D. Ma

发表

Mild method for Ullmann coupling reaction of amines and aryl halides.

D. Ma, Q. Cai, H. Zhang, 2003 .

Amino acid promoted CuI-catalyzed C-N bond formation between aryl halides and amines or N-containing heterocycles.

D. Ma, Q. Cai, H. Zhang, 2005, The Journal of organic chemistry.

First total synthesis of martinellic acid, a naturally occurring bradykinin receptor antagonist.

D. Ma, C. Xia, J. Jiang, 2001, Organic letters.

Total synthesis of (±)-martinelline

Dawei Ma, D. Ma, C. Xia, 2002 .

Aromatic nucleophilic substitution or CuI-catalyzed coupling route to martinellic acid.

D. Ma, C. Xia, Jiqing Jiang, 2003, The Journal of organic chemistry.

Copper/amino acid catalyzed cross-couplings of aryl and vinyl halides with nucleophiles.

D. Ma, Q. Cai, 2008, Accounts of chemical research.

Stereospecific total synthesis of (−)-8-epi-hyperaspine

Wei Zhu, D. Ma, 2003 .

First Total Synthesis of Martinellic Acid, a Naturally Occurring Bradykinin Receptor Antagonist.

D. Ma, C. Xia, Jiqing Jiang, 2001 .

Two-component method to enantiopure quinolizidinones and Indolizidinones. Total synthesis of (-)-lasubine II.

D. Ma, W. Zhu, W. Zhu, 2001, Organic letters.

ENANTIOSELECTIVE SYNTHESES OF TUSSILAGINE AND ISOTUSSILAGINE

D. Ma, Jianhua Zhang, 1998 .

Room Temperature Cu-Catalyzed N-Arylation of Oxazolidinones and Amides with (Hetero)Aryl Iodides.

Subhajit Bhunia, D. Ma, Subhadip De, 2022, Organic letters.

Copper-Catalyzed Coupling Reaction of (Hetero)Aryl Chlorides and Amides.

Junli Yin, D. Ma, Subhadip De, 2017, Organic letters.

Selected Copper-Based Reactions for C-N, C-O, C-S, and C-C Bond Formation.

Subhajit Bhunia, Yongwen Jiang, D. Ma, 2017, Angewandte Chemie.

Modern Ullmann–Goldberg Chemistry: Arylation of N‐Nucleophiles with Aryl Halides

Yongwen Jiang, D. Ma, 2013 .

Copper‐Catalyzed Ligand Promoted Ullmann‐Type Coupling Reactions

Yongwen Jiang, D. Ma, 2010 .

Pd/Cu-catalyzed couplings of β-amino esters with aryl bromides. Synthesis of chiral 1,2,3,4-tetrahydro-4-oxo-2-alkyl-1-quinolines

D. Ma, Jiqing Jiang, 1998 .

A sequential reaction process to assemble polysubstituted indolizidines, quinolizidines and quinolizidine analogues

Wei Zhu, D. Ma, G. Cai, 2006 .

Total Synthesis of (.+‐.)‐Martinelline.

D. Ma, C. Xia, L. Heng, 2003 .

Synthesis and biology of a 7-nitro-2,1,3-benzoxadiazol-4-yl derivative of 2-phenylindole-3-acetamide: a fluorescent probe for the peripheral-type benzodiazepine receptor.

A. Kozikowski, N. Boujrad, M. Kotoula, 1997, Journal of medicinal chemistry.

Oxalic Diamides and tert-Butoxide: Two Types of Ligands Enabling Practical Access to Alkyl Aryl Ethers via Cu-Catalyzed Coupling Reaction.

Li Zhang, Zhixiang Chen, Yongwen Jiang, 2019, Journal of the American Chemical Society.

Studies on the structure-activity relationship of 1,3,3,4-tetra-substituted pyrrolidine embodied CCR5 receptor antagonists. Part 1: Tuning the N-substituents.

J. Deadman, Miao Wang, G. Pei, 2010, Bioorganic & medicinal chemistry letters.

Studies on the structure-activity relationship of 1,3,3,4-tetra-substituted pyrrolidine embodied CCR5 receptor antagonists. Part 2: Discovery of highly potent anti-HIV agents.

J. Deadman, Miao Wang, G. Pei, 2010, Bioorganic & medicinal chemistry letters.

Synthesis and Biological Evaluation of 1,3,3,4‐Tetrasubstituted Pyrrolidine CCR5 Receptor Antagonists. Discovery of a Potent and Orally Bioavailable Anti‐HIV Agent

Kunqian Yu, Hualiang Jiang, Renxiao Wang, 2007, ChemMedChem.

Synthesis and biological activity of l-aminoindan-l,3-dicarboxylic acid, a benzo-analogue of (1S, 3R)-ACPD†

D. Ma, K. Ding, Xin-rong Zhang, 2010 .

Recent advances in the synthesis of ent-kaurane diterpenoids.

D. Ma, Bastien Cacherat, Xiangbo Zhao, 2021, Natural product reports.

Synthesis of Benzofuran Analogue of Go6976, an Isoform‐Selective Protein Kinase C Inhibitor

D. Ma, Xin-rong Zhang, Shi-hui Wu, 2010 .

Synthesis of 7,8-disubstituted benzolactam-V8 and its binding to protein kinase C.

P. Blumberg, A. Kozikowski, N. Lewin, 2001, Bioorganic & medicinal chemistry letters.

Total synthesis of cyclic tetrapeptide FR235222, a potent immunosuppressant that inhibits mammalian histone deacetylases.

D. Pei, D. Ma, B. Zou, 2005, Organic letters.

Synthesis and antitumor activity of cyclodepsipeptide zygosporamide and its analogues.

Jun O. Liu, Yihua Zhang, Feiran Zhang, 2008, Bioorganic & medicinal chemistry letters.

Assembly of Substituted 3-Methyleneisoindolin-1-ones via a CuI/L-Proline-Catalyzed Domino Reaction Process of 2-Bromobenzamides and Terminal Alkynes.

Miao Wang, Yongwen Jiang, D. Ma, 2009 .

Pyridinylpyrimidines selectively inhibit human methionine aminopeptidase-1.

Jun O. Liu, L. Amzel, Renxiao Wang, 2013, Bioorganic & medicinal chemistry.

Pyridinylquinazolines selectively inhibit human methionine aminopeptidase-1 in cells.

Michelle S. Miller, Jun O. Liu, L. Amzel, 2013, Journal of medicinal chemistry.

Total Synthesis of Complex Natural Products via Dearomatization

D. Ma, W. Xie, 2016 .

Modeling, chemistry, and biology of the benzolactam analogues of indolactam V (ILV). 2. Identification of the binding site of the benzolactams in the CRD2 activator-binding domain of PKCdelta and discovery of an ILV analogue of improved isozyme selectivity.

R. Glazer, P. Blumberg, A. Kozikowski, 1997, Journal of medicinal chemistry.

Cu-Mediated Ullmann-Type Cross-Coupling and Industrial Applications in Route Design, Process Development, and Scale-up of Pharmaceutical and Agrochemical Processes

Qiang Yang, D. Ma, Yinsong Zhao, 2022, Organic Process Research & Development.

CuI/Oxalamide Catalyzed Couplings of (Hetero)aryl Chlorides and Phenols for Diaryl Ether Formation.

W. Zhou, Mengyang Fan, Yongwen Jiang, 2016, Angewandte Chemie.

Assembly of N-Containing Heterocycles via Pd- and Cu-Catalyzed C–N Bond Formation Reactions

Yongwen Jiang, D. Ma, 2013 .

Copper(I) Oxide/N,N′‐Bis[(2‐furyl)methyl]oxalamide‐Catalyzed Coupling of (Hetero)aryl Halides and Nitrogen Heterocycles at Low Catalytic Loading

Haibo Wu, D. Ma, Subhadip De, 2017 .

Discovery of N-(Naphthalen-1-yl)-N'-alkyl Oxalamide Ligands Enables Cu-Catalyzed Aryl Amination with High Turnovers.

Subhajit Bhunia, Lu Gan, D. Ma, 2017, Organic letters.

Samarium iodide-mediated C–C bond formation in the total synthesis of natural products

Yang Gao, D. Ma, 2022, Nature Synthesis.

Total Synthesis of Kopsinitarine E

D. Ma, Karre Nagaraju, Dongshun Ni, 2020, Angewandte Chemie.

Total synthesis of kopsinitarine E.

D. Ma, Karre Nagaraju, Dongshun Ni, 2020, Angewandte Chemie.

Synthetic Studies toward Plumisclerin A.

Yang Gao, D. Ma, Yi-Fei Wei, 2019, Organic letters.

Total synthesis of the indole alkaloid (±)- and (+)-methyl N-decarbomethoxychanofruticosinate.

D. Ma, Yi-Fei Wei, Duo Zhao, 2013, Angewandte Chemie.

A convergent route to the Galbulimima alkaloids (-)-GB 13 and (+)-GB 16.

Shouyun Yu, D. Ma, W. Zi, 2010, Angewandte Chemie.

l-Proline Promoted Ullmann-Type Coupling Reactions of Aryl Iodides with Indoles, Pyrroles, Imidazoles or Pyrazoles

D. Ma, Q. Cai, 2004 .

Synthesis and Biological Evaluation of 1,3,3,4‐Tetrasubstituted Pyrrolidine CCR5 Receptor Antagonists. Discovery of a Potent and Orally Bioavailable anti‐HIV Agent.

D. Ma, 2007 .

Polyfunctionalized pyrrolidinones via the coupling of N,N- disubstituted β-amino esters with ethyl glyoxalate

D. Ma, Jiqing Jiang, 1998 .

Cyclobutane derivatives as novel nonpeptidic small molecule agonists of glucagon-like peptide-1 receptor.

H. Su, Qing Liu, Jia-yu Liao, 2012, Journal of medicinal chemistry.

A Scalable Total Synthesis of the Antitumor Agents Et-743 and Lurbinectedin.

Zhigao Zhang, D. Ma, Weiming He, 2019, Angewandte Chemie.

A Scalable Total Synthesis of the Antitumor Agents Et‐743 and Lurbinectedin

Zhigao Zhang, D. Ma, Weiming He, 2019, Angewandte Chemie.

Synthesis of aryl azides and vinyl azides via proline-promoted CuI-catalyzed coupling reactions.

Wei Zhu, D. Ma, 2004, Chemical communications.

Efficient synthesis of pyrrolo[2,3-d]pyrimidines via a Cu(I)/6-methylpicolinic acid catalyzed coupling reaction

Yongwen Jiang, D. Ma, Dequn Sun, 2015 .

Synthesis of 1,2-disubstituted benzimidazoles by a Cu-catalyzed cascade aryl amination/condensation process.

D. Ma, B. Zou, Qiliang Yuan, 2007, Angewandte Chemie.

Design, synthesis, and evaluation of potent, nonpeptidic mimetics of second mitochondria-derived activator of caspases.

Shaomeng Wang, Chao-yie Yang, Z. Nikolovska-Coleska, 2009, Journal of medicinal chemistry.

Cu/N,N'-Dibenzyloxalamide-Catalyzed N-Arylation of Heteroanilines.

Zhixiang Chen, D. Ma, 2019, Organic letters.

Synthesis of a Cyclic Analogue of Galardin

D. Ma, W. Wu, J. Qian, 2010 .

Organocatalytic approach to 3,5,6-trisubstituted and 4,6-disubstituted tetrahydropyran-2-ones

Yihua Zhang, D. Ma, Dan Xu, 2010 .

Synthesis of 7-substituted benzolactam-V8s and their selectivity for protein kinase C isozymes.

A. Kozikowski, Guozhi Tang, D. Ma, 2002, Organic letters.

Synthesis of 7,8-disubstituted benzolactam-V8 and its binding to protein kinase C.

P. Blumberg, A. Kozikowski, N. Lewin, 2001, Bioorganic & medicinal chemistry letters.

Divergent Total Syntheses of Napelline-Type C20-Diterpenoid Alkaloids: (-)-Napelline, (+)-Dehydronapelline, (-)-Songorine, (-)-Songoramine, (-)-Acoapetaldine D, and (-)-Liangshanone.

D. Ma, Xiangbo Zhao, Shicheng Jin, 2022, Journal of the American Chemical Society.

A Unified Approach for the Assembly of Atisine- and Hetidine-type Diterpenoid Alkaloids: Total Syntheses of Azitine and the Proposed Structure of Navirine C.

Jie Liu, D. Ma, 2018, Angewandte Chemie.

Diastereoselective Henry reactions of N,N-dibenzyl α-amino aldehydes with nitromethane catalyzed by enantiopure guanidines

D. Ma, Fu‐She Han, Q. Pan, 2002 .

An efficient and tunable route to AG7088, a rhinovirus protease inhibitor

D. Pei, Q. Lei, D. Ma, 2004, Tetrahedron Letters.

Copper-catalyzed coupling of aryl iodides and tert-butyl β-keto esters: efficient access to α-aryl ketones and α-arylacetic acid tert-butyl esters

Yongwen Jiang, D. Ma, Duo Zhao, 2014 .

Asymmetric synthesis of (−)-deoxoprosophylline

D. Ma, Nan Ma, 2003 .

Mild method for Ullmann coupling reaction of amines and aryl halides.

D. Ma, Q. Cai, H. Zhang, 2003, Organic letters.

CuI-catalyzed coupling reaction of beta-amino acids or esters with aryl halides at temperature lower than that employed in the normal Ullmann reaction. Facile synthesis of SB-214857.

D. Ma, C. Xia, 2001, Organic letters.

A short synthesis of the HIV-protease inhibitor nelfinavir via a diastereoselective addition of ammonia to the α,β-unsaturated sulfoxide derived from (R)-glyceraldehyde acetonide

Wei Zhu, D. Ma, Hua-Dong Xu, 2002 .

Assembly of Primary (Hetero)Arylamines via CuI/Oxalic Diamide-Catalyzed Coupling of Aryl Chlorides and Ammonia.

W. Zhou, Mengyang Fan, Yongwen Jiang, 2015, Organic Letters.

CuI/DMPAO-catalyzed N-arylation of acyclic secondary amines.

D. Ma, Qizheng Yao, Xinye Yang, 2012, Organic letters.

CuI/N,N-dimethylglycine-catalyzed synthesis of N-aryloxazolidinones from aryl bromides

Yihua Zhang, Yongwen Jiang, D. Ma, 2012 .

Assembly of substituted 1H-benzimidazoles and 1,3-dihydrobenzimidazol-2-ones via CuI/L-proline catalyzed coupling of aqueous ammonia with 2-iodoacetanilides and 2-iodophenylcarbamates.

Yongwen Jiang, D. Ma, Yu-Jie Wang, 2009, The Journal of organic chemistry.

Total synthesis and stereochemistry assignment of 15-membered peptide alkaloids abyssenine B and mucronine E

G. He, D. Ma, Jing Wang, 2007 .

Highly convergent route to cyclopeptide alkaloids: total synthesis of ziziphine N.

G. He, D. Ma, Jing Wang, 2007, Organic letters.

Mild and nonracemizing conditions for Ullmann-type diaryl ether formation between aryl iodides and tyrosine derivatives.

G. He, D. Ma, Q. Cai, 2006, The Journal of organic chemistry.

Mild Ullmann-type biaryl ether formation reaction by combination of ortho-substituent and ligand effects.

D. Ma, Q. Cai, B. Zou, 2006, Angewandte Chemie.

CuI/N,N-dimethylglycine-catalyzed coupling of vinyl halides with amides or carbamates.

D. Ma, Q. Cai, Xianhua Pan, 2004, Organic letters.

N,N-dimethyl glycine-promoted Ullmann coupling reaction of phenols and aryl halides.

D. Ma, Q. Cai, 2003, Organic letters.

Synthesis of Aryl Carbamates via Copper‐Catalyzed Coupling of Aryl Halides with Potassium Cyanate

Yihua Zhang, D. Ma, Xinye Yang, 2012 .

Synthesis of 1,5-benzothiazepine dipeptide mimetics via two CuI-catalyzed cross coupling reactions.

D. Ma, J. Gan, 2009, Organic letters.

Synthesis of Aryl Hydrazines via CuI/BMPO Catalyzed Cross-Coupling of Aryl Halides with Hydrazine Hydrate in Water

D. Ma, Siripuram Vijay Kumar, 2018, Chinese Journal of Chemistry.

Palladium catalyzed synthesis of annelated indoles

A. Kozikowski, D. Ma, 1991 .

Synthesis of 2-thio-substituted benzothiazoles via a domino condensation/S-arylation/heterocyclization process.

Liu Shi, Yongwen Jiang, D. Ma, 2011, The Journal of organic chemistry.

Synthesis of 1,5‐Benzothiazepine Dipeptide Mimetics via Two CuI‐Catalyzed Cross Coupling Reactions.

D. Ma, J. Gan, 2009 .

Cascade coupling/cyclization process to N-substituted 1,3-dihydrobenzimidazol-2-ones.

D. Ma, B. Zou, Qiliang Yuan, 2007, Organic letters.

L ‐Proline‐Promoted CuI‐Catalyzed C‐S Bond Formation between Aryl Iodides and Thiols

W. Cao, D. Ma, H. Zhang, 2007 .

A general and efficient approach to aryl thiols: CuI-catalyzed coupling of aryl iodides with sulfur and subsequent reduction.

Jinhua Dong, Yongwen Jiang, D. Ma, 2009, Organic letters.

Assembly of isoquinolines via CuI-catalyzed coupling of beta-keto esters and 2-halobenzylamines.

Yihua Zhang, Yongwen Jiang, D. Ma, 2008, Organic letters.

Enantioselective addition of activated terminal alkynes to 1-acylpyridinium salts catalyzed by Cu-Bis(oxazoline) complexes.

Shouyun Yu, D. Ma, Zhankui Sun, 2007, Journal of the American Chemical Society.

Synthesis of N-(Hetero)aryl Carbamates via CuI/MNAO Catalyzed Cross-Coupling of (Hetero)aryl Halides with Potassium Cyanate in Alcohols.

D. Ma, S. V. Kumar, 2018, The Journal of organic chemistry.

CuI/Oxalic Diamide Catalyzed Coupling Reaction of (Hetero)Aryl Chlorides and Amines.

Wei Zhou, Dawei Ma, Mengyang Fan, 2015, Journal of the American Chemical Society.

Assembly of substituted 3-aminoindazoles from 2-bromobenzonitrile via a CuBr-catalyzed coupling/condensation cascade process.

Yongwen Jiang, D. Ma, Q. Pan, 2013, The Journal of organic chemistry.

Formation of arylboronates by a CuI-catalyzed coupling reaction of pinacolborane with aryl iodides at room temperature

Wei Zhu, D. Ma, 2006 .

A New Class of Amide Ligands Enable Cu‐Catalyzed Coupling of Sodium Methanesulfinate with (Hetero)aryl Chlorides

Yongwen Jiang, Tiemin Sun, D. Ma, 2017 .

Copper-Catalyzed Hydroxylation of (Hetero)aryl Halides under Mild Conditions.

Lu Gan, D. Ma, Kailiang Wang, 2016, Journal of the American Chemical Society.

Efficient and economical access to substituted benzothiazoles: copper-catalyzed coupling of 2-haloanilides with metal sulfides and subsequent condensation.

Peng Xue, Jinhua Dong, Dawei Ma, 2009, Angewandte Chemie.

Assembly of 3-acyloxindoles via cui/L-proline-catalyzed intramolecular arylation of beta-keto amides.

D. Ma, Biao Lu, 2006, Organic letters.

Effect of alteration of the heterocyclic nucleus of ILV on its isoform selectivity for PKC. Palladium catalyzed route to benzofuran analogues of ILV

P. Blumberg, A. Kozikowski, N. Lewin, 1995 .

An efficient synthesis of isocoumarins via a CuI catalyzed cascade reaction process

Yongwen Jiang, D. Ma, Leilei Wang, 2009 .

Assembly of conjugated enynes and substituted indoles via CuI/amino acid-catalyzed coupling of 1-alkynes with vinyl iodides and 2-bromotrifluoroacetanilides.

F. Liu, D. Ma, 2007, The Journal of organic chemistry.

A simple and stereospecfic route to 2,6-disubstituted 4-hydroxypiperidines. Synthesis of dendrobate alkaloid (+)-241D and formal synthesis of (-)-indolizidine 167B.

H. Sun, D. Ma, 2000, Organic letters.

Synthesis of 3-substituted and 2,3-disubstituted quinazolinones via Cu-catalyzed aryl amidation.

Yongwen Jiang, D. Ma, Lanting Xu, 2012, Organic letters.

Synthesis of polysubstituted 1,2-dihydroisoquinolines via a CuI-catalyzed arylation/condensation cascade process

Yihua Zhang, Yongwen Jiang, D. Ma, 2009 .

Assembly of Primary (Hetero)Arylamines via CuI/Oxalic Diamide-Catalyzed Coupling of Aryl Chlorides and Ammonia.

W. Zhou, Mengyang Fan, Yongwen Jiang, 2015, Organic letters.

Synthesis of symmetrical and unsymmetrical N,N'-diaryl guanidines via copper/N-methylglycine-catalyzed arylation of guanidine nitrate.

Yongwen Jiang, Yisheng Lai, D. Ma, 2012, The Journal of organic chemistry.

Synthesis, molecular modeling, 2-D NMR, and biological evaluation of ILV mimics as potential modulators of protein kinase C

Yuan-Ping Pang, Slobodan I Macura, John S. Lazo, 1993 .

AN IMPROVED PROCEDURE TO HOMOCHIRAL CYCLIC STATINES

Jingyuan Ma, D. Ma, L. Dai, 1996 .

Sodium Amalgam, a Useful Reducing Reagent for Formation of Amines from Azides Bearing a Variety of Functional Groups

Jidong Zhu, D. Ma, Biao Lu, 2005 .

Total synthesis of halipeptin A: a potent antiinflammatory cyclic depsipeptide.

Shouyun Yu, Xianfeng Lin, D. Ma, 2005, Angewandte Chemie.

Editorial for the Special Issue on Heterocycles.

D. Comins, D. Ma, 2016, The Journal of organic chemistry.

6-Methylenebicyclo[3.2.1]oct-1-en-3-one: A twisted olefin as Diels-Alder dienophile for expedite syntheses of four kaurane diterpenoids.

D. Ma, Junjie Wang, 2019, Angewandte Chemie.

6‐Methylenebicyclo[3.2.1]oct‐1‐en‐3‐one: A Twisted Olefin as Diels–Alder Dienophile for Expedited Syntheses of Four Kaurane Diterpenoids

D. Ma, Junjie Wang, 2019, Angewandte Chemie.

Synthesis of enantiopure alpha,alpha-disubstituted amino acids from the asymmetric Strecker reaction products of aldehydes.

D. Ma, K. Ding, 2000, Organic letters.

Asymmetric Strecker-Type Reaction of alpha-Aryl Ketones. Synthesis of (S)-alphaM4CPG, (S)-MPPG, (S)-AIDA, and (S)-APICA, the Antagonists of Metabotropic Glutamate Receptors.

D. Ma, Guixiang Zou, H. Tian, 1999, The Journal of organic chemistry.

Assembly of substituted 3-methyleneisoindolin-1-ones via a CuI/l-proline-catalyzed domino reaction process of 2-bromobenzamides and terminal alkynes.

Miao Wang, Yongwen Jiang, D. Ma, 2009, Organic letters.

A one-pot coupling/hydrolysis/condensation process to pyrrolo[1,2-a]quinoxaline.

D. Ma, Qiliang Yuan, 2008, The Journal of organic chemistry.

Elaboration of 2-(trifluoromethyl)indoles via a cascade coupling/condensation/deacylation process.

D. Ma, Yu Chen, Zheming Sun, 2008, Organic letters.

Facile access to polysubstituted indoles via a cascade Cu-catalyzed arylation-condensation process.

D. Ma, Yu Chen, Xiaoan Xie, 2007, The Journal of organic chemistry.

CuI-catalyzed domino process to 2,3-disubstituted benzofurans from 1-bromo-2-iodobenzenes and beta-keto esters.

Yihua Zhang, D. Ma, Bao Wang, 2007, The Journal of organic chemistry.

CuI-catalyzed coupling reaction of aryl halides with terminal alkynes in the absence of palladium and phosphine.

F. Liu, D. Ma, Feng Liu, 2004, Chemical communications.

Oxidative coupling strategies for the synthesis of indole alkaloids.

D. Ma, Karre Nagaraju, 2018, Chemical Society reviews.

Palladium-catalyzed direct functionalization of 2-aminobutanoic acid derivatives: application of a convenient and versatile auxiliary.

Mengyang Fan, D. Ma, 2013, Angewandte Chemie.

Assembly of N,N-disubstituted hydrazines and 1-aryl-1H-indazoles via copper-catalyzed coupling reactions.

Yongwen Jiang, D. Ma, Xiaodong Xiong, 2012, Organic letters.

Enantioselective arylation of 2-methylacetoacetates catalyzed by CuI/trans-4-hydroxy-L-proline at low reaction temperatures.

D. Ma, Yu Chen, Xiaoan Xie, 2006, Journal of the American Chemical Society.

Mild Ullmann-type biaryl ether formation reaction by combination of ortho-substituent and ligand effects.

D. Ma, Q. Cai, B. Zou, 2006, Angewandte Chemie.

CuI/L-proline-catalyzed coupling reactions of aryl halides with activated methylene compounds.

D. Ma, G. Cai, Xiaoan Xie, 2005, Organic letters.

CuI/N,N-Dimethylglycine-Catalyzed Cross-Coupling Reaction of Vinyl Halides with Phenols and its Application to the Assembly of Substituted Benzofurans

D. Ma, Q. Cai, Xiaoan Xie, 2005 .

Synthesis of aryl sulfones via L-proline-promoted CuI-catalyzed coupling reaction of aryl halides with sulfinic acid salts.

Wei Zhu, D. Ma, 2005, The Journal of organic chemistry.

Cu(I)/L-proline-catalyzed coupling of substituted 3-iodoprop-2-en-1-ols with 1-alkynes and subsequent cyclization: a convenient approach for synthesizing polysubstituted furans.

D. Ma, You Wang, Lanting Xu, 2010, Chemistry, an Asian journal.

Highly stereoselective isomerization of ynones to conjugated dienones catalyzed by transition metal complexes

Y. Yu, D. Ma, Xiyan Lu, 1989 .

Stereoselective synthesis of (S)-MPPG, (S)-MTPG and (S)-(+)-αM4CPG from (R)-4-hydroxyphenylglycine

D. Ma, H. Tian, 1997 .

The N-aryl aminocarbonyl ortho-substituent effect in Cu-catalyzed aryl amination and its application in the synthesis of 5-substituted 11-oxo-dibenzodiazepines.

Yongwen Jiang, Yinlong Guo, Wei Zhu, 2011, Organic letters.

Iridium(III)-Catalyzed Regioselective C7-Amination of N-Pivaloylindoles with Sulfonoazides.

L. Tan, D. Ma, Lanting Xu, 2016, The Journal of organic chemistry.

Rhodium-Catalyzed Regioselective C7-Functionalization of N-Pivaloylindoles.

L. Tan, D. Ma, Yu-Peng He, 2016, Angewandte Chemie.

Organocatalytic Michael Addition of Aldehydes to Trisubstituted Nitroolefins.

D. Ma, Leilei Wang, Xiaojing Zhang, 2013 .

Diastereoselective aldol reaction of N,N-dibenzyl-alpha-amino aldehydes with ketones catalyzed by proline.

D. Ma, Q. Pan, Yu-Jie Wang, 2004, Organic letters.

Intramolecular dearomative oxidative coupling of indoles: a unified strategy for the total synthesis of indoline alkaloids.

Z. Zuo, D. Ma, W. Zi, 2015, Accounts of chemical research.

Organocatalytic Michael addition of aldehydes to gamma-keto-alpha,beta-unsaturated esters. an efficient entry to versatile chiral building blocks.

D. Ma, Jing Wang, A. Ma, 2008, Organic letters.

Total synthesis and absolute stereochemical assignment of (-)-communesin F.

Z. Zuo, D. Ma, W. Xie, 2010, Journal of the American Chemical Society.

Total synthesis of the monoterpenoid indole alkaloid (±)-aspidophylline A.

M. Teng, D. Ma, W. Zi, 2014, Angewandte Chemie.

CuBr/N,N-Dimethylglycine-Catalyzed Coupling Reaction of 2-Chlorotrifluoroacetanilides with Phenols at Mild Conditions

Yihua Zhang, Yongwen Jiang, D. Ma, 2010 .

Facile synthesis of 1,4-benzodiazepin-3-ones from o-bromobenzylamines and amino acids via a cascade coupling/condensation process

Yongwen Jiang, D. Ma, Kun Gao, 2009 .

Assembly of Conjugated Enynes and Substituted Indoles via CuI/Amino Acid Catalyzed Coupling of 1‐Alkynes with Vinyl Iodides and 2‐Bromotrifluoroacetanilides.

F. Liu, D. Ma, 2007 .

Highly asymmetric bromocyclization of tryptophol: unexpected accelerating effect of DABCO-derived bromine complex.

Yisheng Lai, D. Ma, Guangde Jiang, 2014, Organic letters.

Total synthesis and cytotoxicity of bisebromoamide and its analogues

Shouyun Yu, D. Ma, Wenhua Li, 2011 .

Organocatalytic approach to polysubstituted piperidines and tetrahydropyrans.

D. Ma, Shaolin Zhu, You Wang, 2011, Organic letters.

Assembly of 4‐Substituted 3‐Nitro‐1,2,3,4‐tetrahydropyridines via Organocatalytic Michael Addition

Yihua Zhang, D. Ma, A. Ma, 2012 .

Stereospecific route to enantiopure all cis-2,3,6-trisubstituted piperidines. Facile synthesis of (-)-deoxocassine and (+)-azimic acid

D. Ma, Nan Ma, 2003 .

Total synthesis of clavepictines A and B and pictamine.

Tiejun Cheng, Renxiao Wang, Shanghai Yu, 2006, Organic letters.

An efficient sequential reaction process to polysubstituted indolizidines and quinolizidines and its application to the total synthesis of indolizidine 223A.

Wei Zhu, D. Ma, X. Pu, 2005, Organic letters.

Prepartion of syn-δ-Hydroxy-β-amino esters via an intramolecular hydrogen bond directed diastereoselective hydrogenation. Total synthesis of (3S,4aS,6R,8S)-hyperaspine

Wei Zhu, D. Ma, 2003 .

Synthesis of enantiopure N-protected 4,5-disubstituted 3-pyrrolidinones and N-protected 2,5-disubstituted 3-pyrrolidinones via the Dieckmann reaction of dicarbonyl compounds derived from enantiopure β-amino esters

D. Ma, Yue Wang, 2001 .

A Simple and Stereospecific Route to 2,6-Disubstituted 4-Hydroxypiperidines. Synthesis of Dendrobate Alkaloid (+)-241D (XII) and Formal Synthesis of (-)-Indolizidine 167B (XVII).

Haiying Sun, D. Ma, 2000 .

Total Synthesis of (2S,3S,4R)-Plakoridine A.

Haiying Sun, D. Ma, 2000 .

Diastereoselective synthesis of 2,4,5-trisubstituted piperidines from enantiopure β-amino esters

Haiying Sun, D. Ma, 1999 .

β-Amino ester route to tussilagine, isotussilagine and (–)-petasinecine

D. Ma, Jianhua Zhang, 1999 .

Total synthesis of leucosceptroids A and B.

Jie Liu, D. Ma, Shengjin Guo, 2015, Angewandte Chemie.

Domino condensation/S-arylation/heterocyclization reactions: copper-catalyzed three-component synthesis of 2-N-substituted benzothiazoles.

Liu Shi, Yongwen Jiang, D. Ma, 2011, Angewandte Chemie.

Assembly of N-substituted pyrrolo[2,1-c][1,4]benzodiazepine-5,11-diones via copper catalyzed aryl amination

Liu Shi, Yongwen Jiang, D. Ma, 2010 .

A flexible route to immunosuppressive agent FR252921. Asymmetric total synthesis of its (13R,14R,19R)-isomer

F. Liu, Shouyun Yu, D. Ma, 2006 .

Assembly of substituted phenothiazines by a sequentially controlled CuI/ L-proline-catalyzed cascade C-S and C-N bond formation.

Yongwen Jiang, D. Ma, H. Zhang, 2010, Angewandte Chemie.

A one-pot formal [4 + 2] cycloaddition approach to substituted piperidines, indolizidines, and quinolizidines. total synthesis of indolizidine (-)-209I.

Shanghai Yu, Wei Zhu, D. Ma, 2005, The Journal of organic chemistry.

Asymmetric total synthesis of (-)-alkaloid 223A and its 6-epimer.

D. Ma, X. Pu, 2003, The Journal of organic chemistry.

Efficient formal synthesis of the dendrobatid alkaloid, indolizidine (−)-209B

Jinyi Wang, D. Ma, X. Pu, 2002 .

Total synthesis of Akuammiline alkaloid (-)-vincorine via intramolecular oxidative coupling.

D. Ma, W. Zi, W. Xie, 2012, Journal of the American Chemical Society.

Synthetic Studies toward Communesins

Z. Zuo, D. Ma, 2011 .

Recent progress on the total synthesis of natural products in China.

Dawei Ma, Qingquan Wu, D. Ma, 2006, Natural product reports.

Asymmetric total syntheses of marine cyclic depsipeptide halipeptins A-D.

Shouyun Yu, D. Ma, Xianhua Pan, 2006, Chemistry.

Highly efficient catalytic system for enantioselective Michael addition of aldehydes to nitroalkenes in water.

Shouyun Yu, D. Ma, Shaolin Zhu, 2008, Angewandte Chemie.

Enantioselective synthesis of functionalized α-amino acids via a chiral guanidine catalyzed Michael addition reaction

D. Ma, Kent Cheng, 1999 .

A formal [3+2] cycloaddition process with nonactivated aziridines to polysubstituted indolizidines.

Wei Zhu, D. Ma, G. Cai, 2005, Organic letters.

Synthesis of enantiopure substituted dihydrofurans via the reaction of (S)-glyceraldehyde acetonide- or Garner aldehyde acetonide-derived enones with sulfonium ylides

Yongwen Jiang, D. Ma, 2002 .

Metal-catalyzed derivatization of C(alpha)-tetrasubstituted amino acids and their use in the synthesis of cyclic peptides.

A. Späth, B. König, D. Ma, 2009, Chemistry, an Asian journal.

Asymmetric synthesis of (S)-1-aminoindan-1,5-dicarboxylic acid and related analogues via intramolecular acylation of enantiopure α,α-disubstituted amino acids

D. Ma, K. Ding, D. Cheng, 2002 .

Enantioselective synthesis of polysubstituted cyclopentanones by organocatalytic double Michael addition reactions.

D. Ma, A. Ma, 2010, Organic letters.

Enantioselective organocatalytic Michael addition of malonates to α,β-unsaturated aldehydes in water

D. Ma, Shaolin Zhu, A. Ma, 2008 .

Enantioselective Organocatalytic Conjugate Addition of Aldehydes to α,β-Unsaturated Thiol Esters

D. Ma, Shaolin Zhu, You Wang, 2009 .

Synthetic studies toward galbulimima alkaloid (-)-GB 13 and (+)-GB 16 and (-)-himgaline.

Shouyun Yu, D. Ma, W. Zi, 2011, Chemistry, an Asian journal.

Enantioselective assembly of substituted dihydropyrones via organocatalytic reaction in water media.

D. Ma, Jing Wang, Xiaojing Zhang, 2008, Organic letters.

Enantioselective assembly of substituted dihydropyrones via organocatalytic reaction in water media.

D. Ma, Jing Wang, Xiaojing Zhang, 2008, Organic letters.

An Efficient Synthesis of Phenol via CuI/8-Hydroxyquinoline-Catalyzed Hydroxylation of Aryl Halides and Potassium Hydroxide

Yongwen Jiang, Wei Liu, D. Ma, 2010 .

Synthesis of Polysubstituted 1,2‐Dihydroisoquinolines via a CuI‐Catalyzed Arylation/Condensation Cascade Process.

Yihua Zhang, Yongwen Jiang, D. Ma, 2009 .

Organocatalytic Michael addition of aldehydes to protected 2-amino-1-nitroethenes: the practical syntheses of oseltamivir (Tamiflu) and substituted 3-aminopyrrolidines.

Shouyun Yu, D. Ma, Shaolin Zhu, 2010, Angewandte Chemie.

Copper-Catalyzed Diaryl Ether Formation from (Hetero)aryl Halides at Low Catalytic Loadings.

W. Zhou, Mengyang Fan, Yisheng Lai, 2017, The Journal of organic chemistry.

Preparation of (R)‐4‐Cyclohexyl‐2,3‐butadien‐1‐ol

Juntao Ye, S. Ma, D. Ma, 2014 .

Total synthesis of antimicrobial and antitumor cyclic depsipeptides.

Wenhua Li, Andreas Schlecker, Dawei Ma, 2010, Chemical communications.

Total synthesis of salinamide A: a potent anti-inflammatory bicyclic depsipeptide.

D. Ma, Li Tan, 2008, Angewandte Chemie.

CuI/N,N-dimethylglycine-catalyzed coupling of vinyl halides with amides or carbamates.

D. Ma, Q. Cai, Xianhua Pan, 2004, Organic letters.

Stereocontrolled cyclopropanation of Garner's aldehyde derived enones

Yongwen Jiang, D. Ma, 2000 .

Enantioselective total syntheses of communesins A and B.

Z. Zuo, D. Ma, Zhiwei Zuo, 2011, Angewandte Chemie.

Total synthesis of piperazimycin A: a cytotoxic cyclic hexadepsipeptide.

D. Ma, Wenhua Li, J. Gan, 2009, Angewandte Chemie.

Synthesis of (2-Arylindol-3-yl)acetamides as Probes of Mitochondrial Steroidogenesis—A New Mechanism for GABAA Receptor Modulation†

J. Auta, A. Kozikowski, M. Guidotti, 1992 .

Convergent Route to ent-Kaurane Diterpenoids: Total Synthesis of Lungshengenin D and 1α,6α-Diacetoxy-ent-kaura-9(11),16-dien-12,15-dione.

Junjie Wang, Dawei Ma, Junjie Wang, 2017, Journal of the American Chemical Society.

Total synthesis of the cyclodepsipeptide apratoxin A and its analogues and assessment of their biological activities.

Jun O. Liu, D. Ma, Xiaoyi Hu, 2006, Chemistry.

Total synthesis of microsclerodermin E.

Jidong Zhu, D. Ma, 2003, Angewandte Chemie.

Diastereoselective construction of continuous all-carbon quaternary centers via intramolecular oxidative coupling reaction

Z. Zuo, D. Ma, W. Zi, 2013 .

A new three-carbon homologating agent for synthesis of α- keto aldehydes

C. Guo, D. Ma, Xiyan Lu, 1991 .

Isomerization of propargylic alcohols catalyzed by an iridium complex

D. Ma, Xiyan Lu, 1989 .

Assembly of indoline-2-carboxylate-embodied dipeptides via Pd-catalyzed C(sp2)-H bond direct functionalization.

Mengyang Fan, D. Ma, Yu-Peng He, 2015, Organic letters.

Asymmetric, Regioselective Bromohydroxylation of 2-Aryl-2-propen-1-ols Catalyzed by Quinine-Derived Catalysts

Yisheng Lai, D. Ma, Ye Zhang, 2013 .

Selective cconversion of pinane into β-pinene catalyzed by an iridium pentahydride complex

D. Ma, Xiyan Lu, Yingrui Lin, 1987 .

Facile synthesis of (2E,4E)-dienoic esters via stereoselective isomerization of 2-ynoic esters

D. Ma, Xiyan Lu, 1989 .

A simple route to α,β-unsaturated aldehydes from prop-2-ynols

D. Ma, Xiyan Lu, 1989 .

CuI/4-hydro-L-proline as a more effective catalytic system for coupling of aryl bromides with N-boc hydrazine and aqueous ammonia.

Yongwen Jiang, Liqin Jiang, D. Ma, 2009, The Journal of organic chemistry.

Cu/ Picolinamides‐Catalyzed Coupling of (Hetero)aryl Halides with Secondary Phosphine Oxides and Phosphite †

Chao Fang, D. Ma, Bang-Guo Wei, 2021, Chinese Journal of Chemistry.

Synthesis of Symmetrical and Unsymmetrical N,N′‐Diaryl Guanidines via Copper/N‐Methylglycine‐Catalyzed Arylation of Guanidine Nitrate.

Yongwen Jiang, Yisheng Lai, D. Ma, 2012 .

N,N'-Bisoxalamides Enhance the Catalytic Activity in Cu-Catalyzed Coupling of (Hetero)Aryl Bromides with Anilines and Secondary Amines.

Subhajit Bhunia, D. Ma, S. V. Kumar, 2017, The Journal of organic chemistry.

A concise route to the proposed structure of lydiamycin B, an antimycobacterial depsipeptide.

D. Ma, Wenhua Li, J. Gan, 2009, Organic letters.

Potentially biomimetic total synthesis and relative stereochemical assignment of (±)-gracilamine.

D. Ma, W. Zi, Songchuan Tian, 2012, Angewandte Chemie.

Highly enantioselective bromocyclization of tryptamines and its application in the synthesis of (-)-chimonanthine.

Yisheng Lai, D. Ma, Jiadong Hu, 2013, Angewandte Chemie.

Asymmetric, protecting-group-free total synthesis of (-)-englerin A.

Qianghui Zhou, D. Ma, Xiaofei Chen, 2010, Angewandte Chemie.

Total synthesis and structure assignment of papuamide B, a potent marine cyclodepsipeptide with anti-HIV properties.

Guangyu Li, D. Ma, W. Zi, 2008, Angewandte Chemie.

2‐Methoxyimino Acetic Acid

D. Ma, C. Martin, 2016 .

Divergent Entry to Gelsedine-Type Alkaloids: Total Syntheses of (-)-Gelsedilam, (-)-Gelsenicine, (-)-Gelsedine, and (-)-Gelsemoxonine.

Yang Gao, D. Ma, Pingluan Wang, 2018, Journal of the American Chemical Society.

Organocatalytic approach for the syntheses of corynantheidol, dihydrocorynantheol, protoemetinol, protoemetine, and mitragynine.

Xuefeng Sun, D. Ma, 2011, Chemistry, an Asian journal.

Total syntheses of (±)-spiroquinazoline, (-)-alantryphenone, (+)-lapatin A, and (-)-quinadoline B.

D. Ma, Ming‐Jung Wu, 2013, Angewandte Chemie.

Total synthesis of kaitocephalin, the first naturally occurring AMPA/KA receptor antagonist.

J. Yang, D. Ma, 2001, Journal of the American Chemical Society.

Stereocontrolled Cyclopropanation of Garner′s Aldehyde Derived Enones.

Yongwen Jiang, D. Ma, 2001 .

Regioselective acylation at the 5- or 6-position of l-tryptophan derivatives

Yongwen Jiang, D. Ma, 2002 .

Facile synthesis of (+)-α-allokainic acid via Pd-catalyzed hydrogenolysis of allyl acetate derived from trans-4-hydroxy-L-proline

P. Deng, Wengen Wu, D. Ma, 2001 .

Accelerating Effect Induced by the Structure of α‐Amino Acid in the Copper‐Catalyzed Coupling Reaction of Aryl Halides with α‐Amino Acids. Synthesis of Benzolactam‐V8.

D. Ma, Shi-hui Wu, Yongdong Zhang, 2010 .

Elaboration of the Oxazepine Ring System via CuI/L‐Proline‐Catalyzed Intramolecular Aryl Amination.

G. Pei, D. Ma, Ben Li, 2008 .

Elaboration of the OxazepineRing System via CuI/l-Proline-Catalyzed IntramolecularAryl Amination

G. Pei, D. Ma, Ben Li, 2008 .

A new methodology to key intermediates for synthesizing polyene compounds

D. Ma, Xiyan Lu, 1990 .

Oxidation of benzylic methylene compounds to ketones with m-chloroperoxybenzoic acid and oxygen

D. Ma, C. Xia, H. Tian, 1999 .

Enantioselective Arylation of 2‐Methylacetoacetates Catalyzed by CuI/trans‐4‐Hydroxy‐L‐proline at Low Reaction Temperatures.

D. Ma, Yu Chen, Xiaoan Xie, 2007 .

Total Synthesis of Lapidilectine B Enabled by Manganese(III)-Mediated Oxidative Cyclization of Indoles.

Mengyang Fan, Yang Gao, D. Ma, 2018, Chemistry.

Total synthesis of microsclerodermin E.

Jidong Zhu, D. Ma, 2003, Angewandte Chemie.

An Improved Procedure to Homochiral Cyclic Statines.

Jingyuan Ma, D. Ma, L. Dai, 1997 .

Conformationally Constrained Analogues ofL-Glutamate as Subtype-Selective Modulators of Metabotropic Glutamate Receptors

D. Ma, 1999 .

General route to 2,4,5-trisubstituted piperidines from enantiopure beta-amino esters. Total synthesis of pseudodistomin B triacetate and pseudodistomin F.

H. Sun, D. Ma, H. Sun, 2000, The Journal of organic chemistry.

Synthesis of Chiral N-Aryl-α-amino Acids by Pd-Cu Catalyzed Couplings of Chiral α-Amino Acids with Aryl Halides

D. Ma, J. Yao, 1997 .

Synthesis of chiral N-aryl-α-amino acids by PdCu catalyzed couplings of chiral α-amino acids with aryl halides

D. Ma, Ji-Yuan Yao, 1996 .

Sodium Amalgam, a Useful Reducing Reagent for Formation of Amines from Azides Bearing a Variety of Functional Groups.

Jidong Zhu, D. Ma, Biao Lu, 2006 .

A copper-catalyzed coupling reaction of vinyl halides and carbazates: application in the assembly of polysubstituted pyrroles.

D. Ma, Chengang Zhou, 2014, Chemical communications.

Cascade annulation of malonic diamides: a concise synthesis of polycyclic pyrroloindolines.

D. Ma, W. Xie, Fenghua Fan, 2012, Chemical communications.

Iridium pentahydride complex catalyzed dehydrogenation of alcohols in the absence of a hydrogen acceptor

D. Ma, Xiyan Lu, Yuan Lin, 1987 .

Total synthesis of halipeptin A: a potent antiinflammatory cyclic depsipeptide.

Shouyun Yu, Xianfeng Lin, D. Ma, 2005, Angewandte Chemie.

N,N -dimethylglycine -promoted ullmann-type coupling reactions of aryl iodides with aliphatic alcohols

W. Cao, D. Ma, H. Zhang, 2007 .

Identification, biochemical and structural evaluation of species-specific inhibitors against type I methionine aminopeptidases.

Jun O. Liu, A. Addlagatta, D. Ma, 2013, Journal of medicinal chemistry.

Total synthesis of cyclic tetrapeptide FR235222, a potent immunosuppressant that inhibits mammalian histone deacetylases.

D. Pei, D. Ma, B. Zou, 2005, Organic letters.

Synthesis of an oxazoline analogue of apratoxin A.

D. Ma, G. Cai, B. Zou, 2003, Organic letters.

Synthesis of the biaryl moiety of the proteasome inhibitors TMC-95 via a ligandless Pd(OAc)2-catalyzed Suzuki-coupling reaction

D. Ma, Qingquan Wu, 2001 .

Enantioselective construction of the oxidized tryptophan fragment of proteasome inhibitors TMC-95A and TMC-95B

D. Ma, Qingquan Wu, 2000 .

Trypanocidal labdane diterpenoids from the seeds of Aframomum aulacocarpos (Zingiberaceae)

J. D. Connolly, B. Ngadjui, D. Ma, 2007 .

CuI-Catalyzed One-Pot Synthesis of Benzothiazolones from 2-Iodoaniline-Derived Carbamates and Sodium Sulfide.

Yihua Zhang, Yongwen Jiang, D. Ma, 2012 .

Migration of trimethylsilyl groups in enolates of silyl esters

D. Ma, R. R. Roberts, P. F. Hudrlik, 1997 .

Synthesis of (2S,1′R,2′R,3′R)-2-(2′,3′-Dicarboxycyclopropyl)-glycine via the Stereochemically Controlled Cyclopropanation of (S)-Glyceraldehyde Acetonide-Derived Enones

Wengen Wu, Yongwen Jiang, Y. Cao, 2000 .

Reinvestigation on total synthesis of kaitocephalin and its isomers

Shouyun Yu, D. Ma, Shaolin Zhu, 2011 .

Ring-Opening Reactions of α,β-Epoxy Silanes with Organocopper Reagents: Reaction at Carbon or Silicon?

D. Ma, P. F. Hudrlik, A. Hudrlik, 1996 .

Structural basis of RasGRP binding to high-affinity PKC ligands.

I. Enyedy, Shaomeng Wang, P. Blumberg, 2002, Journal of medicinal chemistry.

Synthesis of (S)-α-Cyclopropyl-4- phosphonophenylglycine

Wei Zhu, D. Ma, 2001 .

Organocatalytic Michael addition of aldehydes to trisubstituted nitroolefins

D. Ma, Leilei Wang, Xiaojing Zhang, 2012 .

Organocatalytic and scalable synthesis of the anti-influenza drugs zanamivir, laninamivir, and CS-8958.

D. Ma, J. Zhong, Yunsheng Li, 2014, Angewandte Chemie.

Thiourea-Catalyzed Asymmetric Michael Addition of Carbazolones to 2-Chloroacrylonitrile: Total Synthesis of 5,22-Dioxokopsane, Kopsinidine C, and Demethoxycarbonylkopsin

D. Ma, Dongshun Ni, Yi-Fei Wei, 2018, Angewandte Chemie.

Thiourea-Catalyzed Asymmetric Michael Addition of Carbazolones to 2-Chloroacrylonitrile: Total Synthesis of 5,22-Dioxokopsane, Kopsinidine C, and Demethoxycarbonylkopsin.

D. Ma, Dongshun Ni, Yi-Fei Wei, 2018, Angewandte Chemie.

Asymmetric Strecker reaction of γ-keto acids. Facile entry to α-substituted and α,γ-disubstituted glutamic acids

Guozhi Tang, D. Ma, H. Tian, 2004 .

Synthesis of (S)‐α‐Cyclopropyl‐4‐phosphonophenylglycine.

Wei Zhu, D. Ma, 2001 .

Rhodium-Catalyzed Regioselective C7-Functionalization of Indole Derivatives with Acrylates by Using an N-Imino Directing Group

L. Tan, D. Ma, Lanting Xu, 2017, Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry.

CuI/8‐Hydroxyquinalidine Promoted N‐Arylation of Indole and Azoles

Yihua Zhang, Yongwen Jiang, Yisheng Lai, 2012 .

Construction of polycyclic spiro-indolines via an intramolecular oxidative coupling/cyclization cascade reaction process.

D. Ma, W. Xie, Fenghua Fan, 2012, Organic letters.

Synthesis of (2S,1′ S,2′ S)-2-methyl-2-(carboxycyclopropyl)glycine and (S)-2-amino-2-methyl-4-phosphonobutyric acid from l-alanine

Zhenqiang Yang, D. Ma, Jiqing Jiang, 1997 .

Enantioselective syntheses of α-substituted glutamic acids and α,γ-disubstituted glutamic acids by an asymmetric Strecker reaction

Guozhi Tang, D. Ma, Guixiang Zou, 1999 .

Synthesis and biological evaluation of two analogues of (S)- α-methyl -3-carboxyphenylalanine

J. Wroblewski, A. Kozikowski, D. Ma, 1998 .

Facile synthesis of (2S,1'S,2'S)-2-(Carboxycyclopropyl) glycine, an isotype-selective agonist of metabotropic glutamate receptors

D. Ma, Zhaochun Ma, 1997 .

Synthesis and biological activity of cyclic analogues of MPPG and MCPG as metabotropic glutamate receptor antagonists

J. Wroblewski, Hongbin Sun, D. Ma, 1997 .

STEREOSPECIFIC SYNTHESIS OF (1S,3R)-1-AMINOCYCLOPENTANE-1,3-DICARBOXYLIC ACID, A SELECTIVE AGONIST OF METABOTROPIC GLUTAMATE RECEPTORS

Jingyuan Ma, D. Ma, L. Dai, 1997 .

Palladium-Catalyzed Synthesis of Anellated Indoles.

A. Kozikowski, D. Ma, 1992 .

A palladium catalyzed route to a benzofuran analogue of idolactam V (ILV): Effects on PKC isotype selectivity

P. Blumberg, A. Kozikowski, N. Lewin, 1994 .

General and Stereospecific Route to 9-Substituted, 8,9-Disubstituted, and 9,10-Disubstituted Analogues of Benzolactam-V8

P. Blumberg, A. Kozikowski, N. Lewin, 1999 .

Stereospecific synthesis of 9-substituted benzolactam-V8 from L-tyrosine via regioselective aromatic nitration

D. Ma, Wenjun Tang, 1998 .

A xanthone and a polyketide derivative from the leaves of Cassia obtusifolia (Leguminosae)

D. Ma, P. Tane, H. K. Wabo, 2008 .

Assembly of N,N-disubstituted-N′-arylureas via a copper-catalyzed one-pot three-component reaction of aryl bromides, potassium cyanate, and secondary amines

Yihua Zhang, Yongwen Jiang, D. Ma, 2013 .

Synthesis of 1,2,4-Benzotriazines via Copper(I) Iodide/1H-Pyrrole-2-carboxylic Acid Catalyzed Coupling of o-Haloacetanilides and N-Boc Hydrazine

Zhigao Zhang, Yongwen Jiang, D. Ma, 2015, Synlett.

Chiral Guanidine Catalyzed Annulation to the Core Structure of (‐)‐Huperzine A

D. Ma, Q. Pan, 2010 .

Asymmetric synthesis of α,α-disubstituted amino acids by diastereoselective functionalization of enantiopure phenyloxazinones, derivatives of asymmetric Strecker reaction products of aldehydes

D. Ma, K. Ding, 2001 .

Amino acid-promoted Ullmann-type coupling reactions and their applications in organic synthesis

F. Liu, J. Wang, G. He, 2009 .

Amination and Formation of sp2 C-N Bonds

C. Bolm, M. Taillefer, D. Ma, 2013 .

Assembly of α‐(Hetero)aryl Nitriles via Copper‐Catalyzed Coupling Reactions with (Hetero)aryl Chlorides and Bromides

Yongwen Jiang, D. Ma, Ying Chen, 2021, Angewandte Chemie.

Tetrahydroisoquinoline based sulfonamide hydroxamates as potent matrix metalloproteinase inhibitors.

Wengen Wu, Jia Li, D. Ma, 2004, Bioorganic & medicinal chemistry letters.

Ligand-Promoted Rosenmund–von Braun Reaction

D. Ma, Quan Zhang, 2022, Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry.

Facile entry to substituted decahydroquinoline alkaloids. Total synthesis of lepadins A-E and H.

D. Ma, X. Pu, 2006, The Journal of organic chemistry.

Total synthesis of lepadins B, d, e, and h; determination of the configuration of the latter three alkaloids.

D. Ma, X. Pu, 2004, Angewandte Chemie.

Facile Entry to Substituted Decahydroquinoline Alkaloids. Total Synthesis of Lepadins A—E and H.

D. Ma, X. Pu, 2007 .

Total Synthesis of Lepadins B, D, E, and H; Determination of the Configuration of the Latter Three Alkaloids (II).

D. Ma, X. Pu, 2004 .

Synthesis of 2-alkyl-2-arylcyanoacetates via CuI/sodium picolinate-catalyzed direct arylation of α-substituted cyanoacetates

P. Qin, M. Li, Yongwen Jiang, 2013 .

Assembly of α-(Hetero)aryl Nitriles via Cu-Catalyzed Coupling Reactions with (Hetero)aryl Chlorides and Bromides.

Yongwen Jiang, D. Ma, Ying Chen, 2020, Angewandte Chemie.

Synthesis of the benzofuran analogue of ILV, a new protein kinase C(PKC) activator

P. Blumberg, A. Kozikowski, N. Lewin, 1994 .

In Pursuit of Synthetic Efficiency: Convergent Approaches.

Yang Gao, D. Ma, 2021, Accounts of chemical research.

Synthesis and protein kinase C binding activity of benzolactam-V7.

P. Blumberg, A. Kozikowski, S. Wang, 1999, Bioorganic & medicinal chemistry letters.

Pd-Catalyzed Dimethylation of Tyrosine-Derived Picolinamide for Synthesis of (S)-N-Boc-2,6-dimethyltyrosine and Its Analogues.

D. Ma, Chao Zhang, Xiaojing Zhang, 2017, Organic letters.

Intramolecular Dearomative Oxidative Coupling of Indoles: A Unified Strategy for the Total Synthesis of Indoline Alkaloids

D. Ma, W. Zi, Zhiwei Zuo, 2015 .

Cu/Oxalic Diamide-Catalyzed Coupling of Terminal Alkynes with Aryl Halides.

D. Ma, Ying Chen, Lanting Xu, 2023, The Journal of organic chemistry.

Accelerating effect induced by the structure of αamino acid in the copper-catalyzed coupling reaction of aryl halides with α-amino acids. Synthesis of benzolactam-V8

马大为, D. Ma, 张勇达, 1998 .

Selective inhibition of matrix metalloproteinase isozymes and in vivo protection against emphysema by substituted gamma-keto carboxylic acids.

Yong Xu, Renxiao Wang, Jin Ren, 2006, Journal of Medicinal Chemistry.

Development of 3‐Phenyl‐N‐(2‐(3‐phenylureido)ethyl)‐thiophene‐2‐sulfonamide Compounds as Inhibitors of Antiapoptotic Bcl‐2 Family Proteins

Renxiao Wang, Jing-quan Li, Xiaomei Yan, 2014, ChemMedChem.

Selected Copper-Based Reactions for C-N, C-O, C-S, and C-C Bond Formation.

Subhajit Bhunia, Yongwen Jiang, D. Ma, 2017, Angewandte Chemie.

Elaboration of 2-(trifluoromethyl)indoles via a cascade coupling/condensation/deacylation process.

D. Ma, Yu Chen, Zheming Sun, 2008, Organic letters.

Amino acid promoted CuI-catalyzed C-N bond formation between aryl halides and amines or N-containing heterocycles.

D. Ma, Q. Cai, H. Zhang, 2005, The Journal of organic chemistry.

Synthesis of Aryl Azides and Vinyl Azides via Proline‐Promoted CuI‐Catalyzed Coupling Reactions.

Wei Zhu, D. Ma, 2004 .

Preparation of N‐Aryl Compounds by Amino Acid‐Promoted Ullmann‐Type Coupling Reactions.

Wei Zhu, D. Ma, Q. Cai, 2005 .

Stereoselective synthesis of (S)-(+)-αM4CPG, a selective antagonist of metabotropic glutamate receptors

D. Ma, H. Tian, 1996 .

A convergent route to the Galbulimima alkaloids (-)-GB 13 and (+)-GB 16.

Shouyun Yu, D. Ma, W. Zi, 2010, Angewandte Chemie.

Total synthesis and cytotoxicity studies of a cyclic depsipeptide with proposed structure of palau'amide.

D. Ma, B. Zou, K. Long, 2005, Organic letters.

Synthesis of 1,2-disubstituted benzimidazoles by a Cu-catalyzed cascade aryl amination/condensation process.

D. Ma, B. Zou, Qiliang Yuan, 2007, Angewandte Chemie.

Total syntheses of (±)-spiroquinazoline, (-)-alantryphenone, (+)-lapatin A, and (-)-quinadoline B.

D. Ma, Ming‐Jung Wu, 2013, Angewandte Chemie.

Rhodium-Catalyzed Regioselective C7-Functionalization of N-Pivaloylindoles.

L. Tan, D. Ma, Yu-Peng He, 2016, Angewandte Chemie.

Total synthesis of leucosceptroids A and B.

Jie Liu, D. Ma, Shengjin Guo, 2015, Angewandte Chemie.

Total synthesis of antimicrobial and antitumor cyclic depsipeptides.

D. Ma, Wenhua Li, A. Schlecker, 2010, Chemical communications.

A Class of Amide Ligands Enable Cu-Catalyzed Coupling of (Hetero)aryl Halides with Sulfinic Acid Salts under Mild Conditions.

Yongwen Jiang, Tiemin Sun, D. Ma, 2018, The Journal of organic chemistry.

CuI‐Catalyzed Hydroxylation of Aryl Bromides under the Assistance of 5‐Bromo‐2‐(1H‐imidazol‐2‐yl)pyridine and Related Ligands.

Yongwen Jiang, D. Ma, Chengling Jiang, 2011 .

A copper-catalyzed coupling reaction of vinyl halides and carbazates: application in the assembly of polysubstituted pyrroles.

D. Ma, Chengang Zhou, 2014, Chemical communications.

Cyclobutane derivatives as novel nonpeptidic small molecule agonists of glucagon-like peptide-1 receptor.

H. Su, Qing Liu, Jia-yu Liao, 2012, Journal of medicinal chemistry.