Asymmetric Michael Reaction of α-Cyano Esters Catalyzed by Chiral Rh(I) Complexes with a New Optically Active Biphosphine Ligand

Kohji Inagaki; Kyoko Nozaki; Hidemasa Takaya

doi:10.1055/s-1997-712

Asymmetric Michael Reaction of α-Cyano Esters Catalyzed by Chiral Rh(I) Complexes with a New Optically Active Biphosphine Ligand

Synlett ◽

10.1055/s-1997-712 ◽

2004 ◽

Vol 1 (01) ◽

pp. 119-120 ◽

Cited By ~ 16

Author(s):

Kohji Inagaki ◽

Kyoko Nozaki ◽

Hidemasa Takaya

Keyword(s):

Michael Reaction ◽

Optically Active ◽

Asymmetric Michael Reaction

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Cover Picture: Organocatalytic Asymmetric Michael Reaction of Cyclic 1,3-Dicarbonyl Compounds andα,β-Unsaturated Ketones—A Highly Atom-Economic Catalytic One-Step Formation of Optically Active Warfarin Anticoagulant (Angew. Chem. Int. Ed. 40/2003)

Angewandte Chemie International Edition ◽

10.1002/anie.200390597 ◽

2003 ◽

Vol 42 (40) ◽

pp. 4837-4837 ◽

Cited By ~ 1

Author(s):

Nis Halland ◽

Tore Hansen ◽

Karl Anker Jørgensen

Keyword(s):

Michael Reaction ◽

Optically Active ◽

Dicarbonyl Compounds ◽

Unsaturated Ketones ◽

One Step ◽

Asymmetric Michael Reaction

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ChemInform Abstract: Asymmetric Michael Reaction of α-Cyano Esters Catalyzed by Chiral Rh(I) Complexes with a New Optically Active Bisphosphine Ligand.

ChemInform ◽

10.1002/chin.199723040 ◽

2010 ◽

Vol 28 (23) ◽

pp. no-no

Author(s):

K. INAGAKI ◽

K. NOZAKI ◽

H. TAKAYA

Keyword(s):

Michael Reaction ◽

Optically Active ◽

Asymmetric Michael Reaction

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Organocatalytic Asymmetric Michael Reaction of Cyclic 1,3-Dicarbonyl Compounds andα,β-Unsaturated Ketones—A Highly Atom-Economic Catalytic One-Step Formation of Optically Active Warfarin Anticoagulant

Angewandte Chemie ◽

10.1002/ange.200352136 ◽

2003 ◽

Vol 115 (40) ◽

pp. 5105-5107 ◽

Cited By ~ 66

Author(s):

Nis Halland ◽

Tore Hansen ◽

Karl Anker Jørgensen

Keyword(s):

Michael Reaction ◽

Optically Active ◽

Dicarbonyl Compounds ◽

Unsaturated Ketones ◽

One Step ◽

Asymmetric Michael Reaction

Download Full-text

Titelbild: Organocatalytic Asymmetric Michael Reaction of Cyclic 1,3-Dicarbonyl Compounds andα,β-Unsaturated Ketones—A Highly Atom-Economic Catalytic One-Step Formation of Optically Active Warfarin Anticoagulant (Angew. Chem. 40/2003)

Angewandte Chemie ◽

10.1002/ange.200390624 ◽

2003 ◽

Vol 115 (40) ◽

pp. 4985-4985

Author(s):

Nis Halland ◽

Tore Hansen ◽

Karl Anker Jørgensen

Keyword(s):

Michael Reaction ◽

Optically Active ◽

Dicarbonyl Compounds ◽

Unsaturated Ketones ◽

One Step ◽

Asymmetric Michael Reaction

Download Full-text

Organocatalytic Asymmetric Michael Reaction of Cyclic 1,3-Dicarbonyl Compounds andα,β-Unsaturated Ketones—A Highly Atom-Economic Catalytic One-Step Formation of Optically Active Warfarin Anticoagulant

Angewandte Chemie International Edition ◽

10.1002/anie.200352136 ◽

2003 ◽

Vol 42 (40) ◽

pp. 4955-4957 ◽

Cited By ~ 200

Author(s):

Nis Halland ◽

Tore Hansen ◽

Karl Anker Jørgensen

Keyword(s):

Michael Reaction ◽

Optically Active ◽

Dicarbonyl Compounds ◽

Unsaturated Ketones ◽

One Step ◽

Asymmetric Michael Reaction

Download Full-text

Organocatalytic Asymmetric Michael Reaction of Cyclic 1,3-Dicarbonyl Compounds and α,β-Unsaturated Ketones — A Highly Atom-Economic Catalytic One-Step Formation of Optically Active Warfarin Anticoagulant.

ChemInform ◽

10.1002/chin.200406024 ◽

2004 ◽

Vol 35 (6) ◽

Author(s):

Nis Halland ◽

Tore Hansen ◽

Karl Anker Joergensen

Keyword(s):

Michael Reaction ◽

Optically Active ◽

Dicarbonyl Compounds ◽

Unsaturated Ketones ◽

One Step ◽

Asymmetric Michael Reaction

Download Full-text

ChemInform Abstract: High Diastereoselectivity Induced by a Fluorous Alkyl Group in the Asymmetric Michael Reaction of Nitroalkenes Catalyzed by a Prolinol Methyl Ether.

ChemInform ◽

10.1002/chin.201418075 ◽

2014 ◽

Vol 45 (18) ◽

pp. no-no

Author(s):

Kazumasa Funabiki ◽

Masaya Ohta ◽

Yuta Sakaida ◽

Kiyofumi Oida ◽

Yasuhiro Kubota ◽

...

Keyword(s):

Methyl Ether ◽

Alkyl Group ◽

Michael Reaction ◽

Asymmetric Michael Reaction

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Diastereoselective synthesis of (−)-1-methyl-(3S,4R)-3,4-bis((2S)-N-(tert-butyloxycarbonyl)pyrrolidin-2-yl)-2-pyrrolidinone by an asymmetric Michael reaction

Tetrahedron Asymmetry ◽

10.1016/s0957-4166(98)00241-9 ◽

1998 ◽

Vol 9 (13) ◽

pp. 2369-2376 ◽

Cited By ~ 5

Author(s):

Siavosh Mahboobi ◽

Alfred Popp ◽

Thomas Burgemeister ◽

Dieter Schollmeyer

Keyword(s):

Michael Reaction ◽

Diastereoselective Synthesis ◽

Asymmetric Michael Reaction

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Methyl methacrylate as acceptor in the asymmetric Michael reaction using chiral β-enaminoesters: Simultaneous, complete stereocontrol of a quaternary carbon center and a tertiary one in the β-position

Tetrahedron Asymmetry ◽

10.1016/0957-4166(94)00356-g ◽

1995 ◽

Vol 6 (1) ◽

pp. 79-82 ◽

Cited By ~ 17

Author(s):

Christian Cavé ◽

Valérie Daley ◽

Jean d'Angelo ◽

André Guingant

Keyword(s):

Methyl Methacrylate ◽

Michael Reaction ◽

Quaternary Carbon ◽

Asymmetric Michael Reaction

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Cationic [2,6-Bis(2‘-oxazolinyl)phenyl]palladium(II) Complexes: Catalysts for the Asymmetric Michael Reaction

Organometallics ◽

10.1021/om990710h ◽

2000 ◽

Vol 19 (7) ◽

pp. 1282-1291 ◽

Cited By ~ 116

Author(s):

Mark A. Stark ◽

Geraint Jones ◽

Christopher J. Richards

Keyword(s):

Michael Reaction ◽

Asymmetric Michael Reaction

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