Atroposelective remote meta-C–H activation
暂无分享,去创建一个
jin-quan yu | Peng Wang | Jiahui Zhao | Jian-jun Li | Huan Shen | K. Wu | Xin Kuang
[1] A. Lledós,et al. Palladium-Catalyzed Ortho C–H Arylation of Unprotected Anilines: Chemo- and Regioselectivity Enabled by the Cooperating Ligand [2,2′-Bipyridin]-6(1H)-one , 2022, ACS catalysis.
[2] S. You,et al. Synthesis of Atropisomers by Transition-Metal-Catalyzed Asymmetric C-H Functionalization Reactions. , 2021, Journal of the American Chemical Society.
[3] B. Tan,et al. Recent Advances in Catalytic Asymmetric Construction of Atropisomers. , 2021, Chemical reviews.
[4] D. Blackmond,et al. Insights into the Role of Transient Chiral Mediators and Pyridone Ligands in Asymmetric Pd-Catalyzed C-H Functionalization. , 2020, Journal of Organic Chemistry.
[5] Bing‐Feng Shi,et al. Transition Metal-Catalyzed Enantioselective C-H Functionalization via Chiral Transient Directing Group Strategy. , 2020, Angewandte Chemie.
[6] W. Gu,et al. Enantioselective Cross-Coupling for Axially Chiral Tetra-ortho-Substituted Biaryls and Asymmetric Synthesis of Gossypol. , 2020, Journal of the American Chemical Society.
[7] Robert J. Phipps,et al. Enantioselective remote C–H activation directed by a chiral cation , 2020, Science.
[8] Qi‐Jun Yao,et al. Recent advances in the synthesis of axially chiral biaryls via transition metal-catalysed asymmetric C-H functionalization. , 2019, Chemical communications.
[9] Huan‐Chang Hsiao,et al. Palladium-Catalyzed Benzofulvenation of o -Arylanilines through C−H Bond Activation by Using Two Diarylacetylenes as an Implicit Benzofulvene , 2019, Advanced Synthesis & Catalysis.
[10] Scott J. Miller,et al. Peptide-Based Catalysts Reach the Outer Sphere through Remote Desymmetrization and Atroposelectivity , 2018, Accounts of chemical research.
[11] jin-quan yu,et al. Enantioselective remote meta-C–H arylation and alkylation via a chiral transient mediator , 2018, Nature.
[12] K. Zhao,et al. Enhanced Reactivity by Torsional Strain of Cyclic Diaryliodonium in Cu-Catalyzed Enantioselective Ring-Opening Reaction , 2018 .
[13] jin-quan yu,et al. Ligand-Enabled meta-Selective C-H Arylation of Nosyl-Protected Phenethylamines, Benzylamines, and 2-Aryl Anilines. , 2017, Journal of the American Chemical Society.
[14] M. Fontana,et al. Pd/Norbornene: A Winning Combination for Selective Aromatic Functionalization via C-H Bond Activation. , 2016, Accounts of chemical research.
[15] P. Keller,et al. A twist of nature--the significance of atropisomers in biological systems. , 2015, Natural product reports.
[16] jin-quan yu,et al. Ligand-Enabled Meta-C-H Alkylation and Arylation Using a Modified Norbornene. , 2015, Journal of the American Chemical Society.
[17] Guangbin Dong,et al. Simple Amine-Directed Meta-Selective C-H Arylation via Pd/Norbornene Catalysis. , 2015, Journal of the American Chemical Society.
[18] W. Gong,et al. Ligand-enabled meta-C–H activation using a transient mediator , 2015, Nature.
[19] Y. Ichikawa,et al. Enantioselective synthesis of multisubstituted biaryl skeleton by chiral phosphoric acid catalyzed desymmetrization/kinetic resolution sequence. , 2013, Journal of the American Chemical Society.
[20] Yuhong Zhang,et al. Free-amine-directed alkenylation of C(sp2)-H and cycloamination by palladium catalysis. , 2012, Chemistry.
[21] L. Pu. Enantioselective fluorescent sensors: a tale of BINOL. , 2012, Accounts of chemical research.
[22] O. Hucke,et al. Assessing atropisomer axial chirality in drug discovery and development. , 2011, Journal of medicinal chemistry.
[23] G. Bringmann,et al. Atroposelective total synthesis of axially chiral biaryl natural products. , 2011, Chemical reviews.
[24] Scott J. Miller,et al. Dynamic Kinetic Resolution of Biaryl Atropisomers via Peptide-Catalyzed Asymmetric Bromination , 2010, Science.
[25] S. LaPlante,et al. The challenge of atropisomerism in drug discovery. , 2009, Angewandte Chemie.
[26] Nicola Della Ca’,et al. Catalytic sequential reactions involving palladacycle-directed aryl coupling steps. , 2008, Accounts of chemical research.
[27] J. W. Doane,et al. Reversible photoswitchable axially chiral dopants with high helical twisting power. , 2007, Journal of the American Chemical Society.
[28] Masakatsu Shibasaki,et al. Design and application of linked-BINOL chiral ligands in bifunctional asymmetric catalysis. , 2006, Chemical Society reviews.
[29] J. Brunel. BINOL: a versatile chiral reagent. , 2005, Chemical reviews.
[30] A. Yudin,et al. Modified BINOL ligands in asymmetric catalysis. , 2003, Chemical reviews.
[31] S. Vyskocil,et al. Non-symmetrically substituted 1,1'-binaphthyls in enantioselective catalysis. , 2003, Chemical reviews.
[32] S. Buchwald,et al. Catalytic asymmetric vinylation of ketone enolates. , 2001, Organic letters.
[33] S. Buchwald,et al. A Catalytic Asymmetric Suzuki Coupling for the Synthesis of Axially Chiral Biaryl Compounds , 2000 .
[34] P. Wipf,et al. Formal Total Synthesis of (+)-Diepoxin σ , 2000 .
[35] S. Murai,et al. Atropselective alkylation of biaryl compounds by means of transition metal-catalyzed C–H/olefin coupling , 2000 .
[36] Tamio Hayashi,et al. Chiral monodentate phosphine ligand MOP for transition-metal-catalyzed asymmetric reactions. , 2000, Accounts of chemical research.
[37] S. Vyskocil,et al. Derivatives of 2-Amino-2‘-diphenylphosphino-1,1‘-binaphthyl (MAP) and Their Application in Asymmetric Palladium(0)-Catalyzed Allylic Substitution† , 1998 .
[38] K. Gothelf,et al. A Simple Synthetic Approach to 3,3'-Diaryl BINOLs. , 1998, The Journal of organic chemistry.
[39] Armando Rangoni,et al. A Complex Catalytic Cycle Leading to a Regioselective Synthesis of o,o′‐Disubstituted Vinylarenes , 1997 .
[40] D. Cai,et al. Simple and efficient resolution of l,1′-bi-2-naphthol , 1995 .
[41] P. Sedmera,et al. Synthesis of enantiomerically pure 2,2'-dihydroxy-1,1'-binaphthyl, 2,2'-diamino-1,1'-binaphthyl, and 2-amino-2'-hydroxy-1,1'-binaphthyl. Comparison of processes operating as diastereoselective crystallization and as second order asymmetric transformation , 1992 .
[42] R. Noyori,et al. BINAP: an efficient chiral element for asymmetric catalysis , 1990 .
[43] R. Noyori,et al. Practical synthesis of (R)- or (S)-2,2'-bis(diarylphosphino)-1,1'-binaphthyls (BINAPs) , 1986 .
[44] Wenjun Tang,et al. Efficient Enantioselective Syntheses of Chiral Natural Products Facilitated by Ligand Design. , 2019, Chemical record.
[45] A. Cammidge,et al. The first asymmetric Suzuki cross-coupling reaction , 2000 .