K. Ding

发表

Copper-catalyzed tandem reaction of isocyanides with N-(2-haloaryl)propiolamides for the synthesis of pyrrolo[3,2-c]quinolin-4-ones.

F. Zhou, Jianguang Liu, Q. Cai, 2011, The Journal of organic chemistry.

2-Pyridinyl beta-ketones as new ligands for room-temperature CuI-catalysed C-N coupling reactions.

Deping Wang, K. Ding, 2009, Chemical communications.

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 .

Structure-activity study on a series of α-glutamic acid scaffold based compounds as new ADAMTS inhibitors.

Honglin Li, Xiaofeng Liu, Lei Duan, 2011, Bioorganic & Medicinal Chemistry Letters.

Mild Conditions for Copper-CatalyzedN-Arylation of Imidazoles

Huaming Chen, Deping Wang, Q. Cai, 2010 .

A CuAAC/Ullmann C-C coupling tandem reaction: copper-catalyzed reactions of organic azides with N-(2-iodoaryl)propiolamides or 2-iodo-N-(prop-2-ynyl)benzenamines.

Q. Cai, K. Ding, Jiajie Yan, 2012, Organic letters.

Copper‐Mediated Diamination of Arylboronic Acids for the Synthesis of 2‐Aryl Benzimidazoles Using Trimethylsilyl Azide as the Amino Sources with Aldehydes

F. Zhou, K. Ding, Zeqiang Xie, 2020 .

Synthesis of 1-Aryl-1H-indazoles via a Ligand-Free Copper- Catalyzed Intramolecular Amination Reaction

Q. Cai, K. Ding, Xianyang Wang, 2011 .

Copper-catalyzed tandem reactions of 1-(2-iodoary)-2-yn-1-ones with isocyanides for the synthesis of 4-oxo-indeno[1,2-b]pyrroles.

F. Zhou, Q. Cai, K. Ding, 2011, Organic letters.

Enantioselective [4+2] cycloadditions of 2-vinyl-1H-indoles with 3-nitro-2H-chromenes catalyzed by a Zn(OTf)2/bis(oxazoline) complex: an efficient approach to fused heterocycles with a quaternary stereocenter.

W. Xiao, Fen Tan, Cong Xiao, 2012, Chemistry, an Asian journal.

Manganese-Catalyzed C−H Annulation of Ketimines with Allenes: Stereoselective Synthesis of 1-Aminoindanes

K. Ding, Lijie Peng, Chong Lei, 2018, Advanced Synthesis & Catalysis.

(2-Pyridyl)acetone-promoted Cu-catalyzed O-arylation of phenols with aryl iodides, bromides, and chlorides.

Deping Wang, Qi Zhang, K. Ding, 2009, The Journal of organic chemistry.

Palladium-catalyzed amidation of N-tosylhydrazones with isocyanides.

F. Zhou, Q. Cai, K. Ding, 2011, Chemistry.

An Efficient Copper-Catalyzed Amination of Aryl Halides by Aqueous Ammonia

Deping Wang, Q. Cai, K. Ding, 2009 .

Copper‐Catalyzed Tandem Reaction of Isocyanides with N‐(2‐Haloaryl)propiolamides for the Synthesis of Pyrrolo[3,2‐c]quinolin‐4‐ones.

F. Zhou, Jianguang Liu, Q. Cai, 2011 .

An Efficient Copper‐Catalyzed Amination of Aryl Halides by Aqueous Ammonia.

Deping Wang, Q. Cai, K. Ding, 2010 .

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

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

Synthesis of [1,2,3]triazolo[1,5-a]quinoxalin-4(5H)-ones through copper-catalyzed tandem reactions of N-(2-haloaryl)propiolamides with sodium azide.

F. Zhou, Q. Cai, K. Ding, 2012, Organic letters.

Assembly of indole-2-carboxylic acid esters through a ligand-free copper-catalysed cascade process.

D. Pei, Zhengqiu Li, Q. Cai, 2009, Chemical communications.

Copper-catalyzed desymmetric intramolecular Ullmann C-N coupling: an enantioselective preparation of indolines.

F. Zhou, Jianguang Liu, Jiajia Guo, 2012, Journal of the American Chemical Society.

Identification of pyrido[1,2-α]pyrimidine-4-ones as new molecules improving the transcriptional functions of estrogen-related receptor α.

Xuefei Gao, Lei Duan, Donghai Wu, 2011, Journal of medicinal chemistry.

Synthesis of aza-fused polycyclic quinolines through copper-catalyzed cascade reactions.

D. Pei, Zhengqiu Li, Q. Cai, 2010, Organic letters.

Chemoselective synthesis of biheterocyclic skeletons tetrahydro-1H-pyrrolo[1,2-c]imidazole and tetrahydropyrrolo[1,2-c]thiazole derivatives via multicomponent self-sorting domino strategy

A. Wu, Cheng Xu, Fengcheng Jia, 2015 .

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 .

Enantio- and Diastereodivergent Synthetic Route to Multifarious Cyclitols from D-Xylose via Ring-Closing Metathesis.

A. Kornienko, M. d'Alarcao, K. Ding, 2008, Synthesis.

Direct Oxidation of N‐Benzylamides to Aldehydes or Ketones by N‐Bromosuccinimide

K. Ding, Guan-Hua Wang, C. Ha, 2008 .

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 .

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.

An Efficient Synthesis of ABT-263, a Novel Inhibitor of Antiapoptotic Bcl-2 Proteins

D. Pei, K. Ding, Hu-Shan Zhang, 2008 .

2-Pyridinyl beta-ketones as new ligands for room-temperature CuI-catalysed C-N coupling reactions.

Deping Wang, K. Ding, 2009, Chemical communications.

Copper-catalyzed desymmetric intramolecular Ullmann C-N coupling: an enantioselective preparation of indolines.

F. Zhou, Jianguang Liu, Jiajia Guo, 2012, Journal of the American Chemical Society.