ChemInform Abstract: Highly Efficient Enantioselective Synthesis of Optically Active Dihydropyrones by Chiral Titanium(IV) (5,5′,6,6′,7,7′,8,8′-Octahydro-1,1′-bi-2-naphthol) Complexes.

Bin Wang; Xiaoming Feng; Xin Cui; Hui Liu; Yaozhong Jiang

doi:10.1002/chin.200048151

ChemInform Abstract: Highly Efficient Enantioselective Synthesis of Optically Active Dihydropyrones by Chiral Titanium(IV) (5,5′,6,6′,7,7′,8,8′-Octahydro-1,1′-bi-2-naphthol) Complexes.

ChemInform ◽

10.1002/chin.200048151 ◽

2000 ◽

Vol 31 (48) ◽

pp. no-no

Author(s):

Bin Wang ◽

Xiaoming Feng ◽

Xin Cui ◽

Hui Liu ◽

Yaozhong Jiang

Keyword(s):

Optically Active ◽

Enantioselective Synthesis ◽

Highly Efficient

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Mechanistic switch leading to highly efficient chirality transfer in Pd(0)-catalyzed couplingâ€“cyclization of aryl iodides with 1âˆ¶1 acidâ€“base salts of 2,3-allenoic acids and l-(â€“)-cinchonidine or d-(+)-/l-(â€“)-Î±-methylbenzylamine. Enantioselective synthesis of highly optically active 3-aryl polysubstituted butenolidesElectronic supplementary information (ESI) available: experimental details. See http://www.rsc.org/suppdata/cc/b1/b109645a/

Chemical Communications ◽

10.1039/b109645a ◽

2002 ◽

pp. 540-541 ◽

Cited By ~ 30

Author(s):

Shengming Ma ◽

Zhangjie Shi

Keyword(s):

Optically Active ◽

Enantioselective Synthesis ◽

Supplementary Information ◽

Chirality Transfer ◽

Highly Efficient ◽

Aryl Iodides

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ChemInform Abstract: Highly Efficient Enantioselective Synthesis of Optically Active Carboxylic Acids by Ru(OCOCH3)2((S)-H8-BINAP).

ChemInform ◽

10.1002/chin.199702040 ◽

2010 ◽

Vol 28 (2) ◽

pp. no-no

Author(s):

T. UEMURA ◽

X. ZHANG ◽

K. MATSUMURA ◽

N. SAYO ◽

H. KUMOBAYASHI ◽

...

Keyword(s):

Carboxylic Acids ◽

Optically Active ◽

Enantioselective Synthesis ◽

Highly Efficient

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Highly Efficient Enantioselective Synthesis of Optically Active Carboxylic Acids by Ru(OCOCH3)2[(S)-H8-BINAP]

The Journal of Organic Chemistry ◽

10.1021/jo960426p ◽

1996 ◽

Vol 61 (16) ◽

pp. 5510-5516 ◽

Cited By ~ 105

Author(s):

Toshitsugi Uemura ◽

Xiaoyoung Zhang ◽

Kazuhiko Matsumura ◽

Noboru Sayo ◽

Hidenori Kumobayashi ◽

...

Keyword(s):

Carboxylic Acids ◽

Optically Active ◽

Enantioselective Synthesis ◽

Highly Efficient

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Highly efficient enantioselective synthesis of optically active dihydropyrones by chiral titanium(iv) (5,5′,6,6′,7,7′,8,8′-octahydro-1,1′-bi-2-naphthol) complexes

Chemical Communications ◽

10.1039/b004813p ◽

2000 ◽

pp. 1605-1606 ◽

Cited By ~ 31

Author(s):

Bin Wang ◽

Xiaoming Feng ◽

Xin Cui ◽

Hui Liu ◽

Yaozhong Jiang

Keyword(s):

Optically Active ◽

Enantioselective Synthesis ◽

Highly Efficient

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The Catalytic Enantioselective Synthesis of Optically Active Epoxides and Tetrahydrofurans.Asymmetric Epoxidation, the Desymmetrization of meso-Tetrahydrofurans, and Enantiospecific Ring-Enlargement

Current Organic Chemistry ◽

10.2174/1385272013375364 ◽

2001 ◽

Vol 5 (6) ◽

pp. 663-678 ◽

Cited By ~ 45

Author(s):

Tsutomu Katsuki

Keyword(s):

Optically Active ◽

Enantioselective Synthesis ◽

Ring Enlargement

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Enantioselective synthesis of tetrahydroisoquinolines via catalytic intramolecular asymmetric reductive amination

Organic Chemistry Frontiers ◽

10.1039/d0qo01554g ◽

2021 ◽

Author(s):

Ruixia Liu ◽

Jingkuo Han ◽

Bin Li ◽

Xian Liu ◽

Zhao Wei ◽

...

Keyword(s):

Reductive Amination ◽

Enantioselective Synthesis ◽

Iridium Complex ◽

Highly Efficient ◽

Efficient Access

A highly efficient intramolecular asymmetric reductive amination transformation catalyzed by an iridium complex of tBu-ax-Josiphos has been realized, providing an efficient access to various THIQ alkaloids.

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Enantioselective synthesis of optically active cis-β-thio-α-amino acid derivatives through an organocatalytic cascade thio-Michael/ring opening process

Chemical Communications ◽

10.1039/c2cc30799e ◽

2012 ◽

Vol 48 (39) ◽

pp. 4713 ◽

Cited By ~ 22

Author(s):

Zhi-Cong Geng ◽

Ning Li ◽

Jian Chen ◽

Xiao-Fei Huang ◽

Bin Wu ◽

...

Keyword(s):

Amino Acid ◽

Ring Opening ◽

Optically Active ◽

Enantioselective Synthesis ◽

Amino Acid Derivatives ◽

Opening Process

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Asymmetric Diboration of Terminal Alkenes with a Rhodium Catalyst and Subsequent Oxidation: Enantioselective Synthesis of Optically Active 1,2-Diols

Angewandte Chemie ◽

10.1002/ange.201305181 ◽

2013 ◽

Vol 125 (42) ◽

pp. 11217-11221 ◽

Cited By ~ 19

Author(s):

Kenji Toribatake ◽

Hisao Nishiyama

Keyword(s):

Rhodium Catalyst ◽

Optically Active ◽

Enantioselective Synthesis ◽

Subsequent Oxidation ◽

Terminal Alkenes

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Enantioselective synthesis of optically active β-aminoalcohols via asymmetric reduction

Tetrahedron Asymmetry ◽

10.1016/s0957-4166(00)80269-4 ◽

1992 ◽

Vol 3 (3) ◽

pp. 341-342 ◽

Cited By ~ 27

Author(s):

Byung Tae Cho ◽

Yu Sung Chun

Keyword(s):

Asymmetric Reduction ◽

Optically Active ◽

Enantioselective Synthesis

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ChemInform Abstract: Asymmetric Ion Pair Catalysis of 6π Electrocyclizations: Broensted Acid Catalyzed Enantioselective Synthesis of Optically Active 1,4-Dihydropyridazines.

ChemInform ◽

10.1002/chin.201351184 ◽

2013 ◽

Vol 44 (51) ◽

pp. no-no

Author(s):

Arindam Das ◽

Chandra M. R. Volla ◽

Iuliana Atodiresei ◽

Wolfgang Bettray ◽

Magnus Rueping

Keyword(s):

Ion Pair ◽

Optically Active ◽

Enantioselective Synthesis ◽

Acid Catalyzed

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