Solid-Phase Development of Chiral Phosphoramidite Ligands for Enantioselective Conjugate Addition Reactions

Chemistry - A European Journal ◽

10.1002/1521-3765(20021018)8:20<4767::aid-chem4767>3.0.co;2-o ◽

2002 ◽

Vol 8 (20) ◽

pp. 4767-4780 ◽

Author(s):

Oliver Huttenloch ◽

Eltepu Laxman ◽

Herbert Waldmann

Keyword(s):

Solid Phase ◽

Conjugate Addition ◽

Addition Reactions ◽

Phase Development

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Solid phase aldol and conjugate addition reactions using Evans' oxazolidinone chiral auxiliary

Tetrahedron Letters ◽

10.1016/s0040-4039(98)00230-5 ◽

1998 ◽

Vol 39 (17) ◽

pp. 2655-2658 ◽

Author(s):

Chee Wee Phoon ◽

Chris Abell

Keyword(s):

Solid Phase ◽

Conjugate Addition ◽

Chiral Auxiliary ◽

Addition Reactions

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Oxadiazinones as chiral auxiliaries: Asymmetric conjugate addition reactions with Ephedra based oxadiazinones

10.1021/scimeetings.0c01411 ◽

2020 ◽

Author(s):

Fatima Olayemi Obe ◽

Shawn Hitchcock

Keyword(s):

Conjugate Addition ◽

Addition Reactions ◽

Chiral Auxiliaries

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Recent Advances in Photoredox‐Mediated Radical Conjugate Addition Reactions: An Expanding Toolkit for the Giese Reaction

Angewandte Chemie ◽

10.1002/ange.202016666 ◽

2021 ◽

Author(s):

Anastasia L. Gant Kanegusuku ◽

Jennifer L Roizen

Keyword(s):

Conjugate Addition ◽

Addition Reactions ◽

Recent Advances

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ChemInform Abstract: Peptide-Catalyzed Stereoselective Conjugate Addition Reactions Generating All-Carbon Quaternary Stereogenic Centers.

10.1002/chin.201348091 ◽

2013 ◽

Vol 44 (48) ◽

pp. no-no

Author(s):

Robert Kastl ◽

Helma Wennemers

Keyword(s):

Conjugate Addition ◽

Addition Reactions ◽

Stereogenic Centers ◽

Quaternary Stereogenic Centers

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Unusual O-Conjugate Addition Reactions of β-Ketoesters and 1,3-Diketones to Ethyl Propynoate: Applications to the Synthesis of Furans.

10.1002/chin.200322071 ◽

2003 ◽

Vol 34 (22) ◽

Author(s):

Jinsung Tae ◽

Kwang-Ok Kim

Keyword(s):

Conjugate Addition ◽

Addition Reactions

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Corrigendum to “Advances on asymmetric organocatalytic 1,4-conjugate addition reactions in aqueous and semi-aqueous media” [Tetrahedron: Asymmetry 2017, 849–875]

Tetrahedron Asymmetry ◽

10.1016/j.tetasy.2017.10.009 ◽

2017 ◽

Author(s):

Anirban Mondal ◽

Sudipto Bhowmick ◽

Ayndrila Ghosh ◽

Tanmoy Chanda ◽

Kartick C. Bhowmick

Keyword(s):

Aqueous Media ◽

Conjugate Addition ◽

Addition Reactions

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Conjugate addition reactions of some magnesium-based organocuprates with α-ethylenic carbonyl compounds

Journal of Organometallic Chemistry ◽

10.1016/s0022-328x(00)84517-9 ◽

1980 ◽

Vol 199 (1) ◽

pp. 9-14 ◽

Author(s):

M.T. Rahman ◽

S.L. Saha ◽

A.-T. Hansson

Keyword(s):

Carbonyl Compounds ◽

Conjugate Addition ◽

Addition Reactions

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(Trimethylstannyl)vinyl Cuprates: Generation and Conjugate Addition Reactions

The Journal of Organic Chemistry ◽

10.1021/jo960245n ◽

1996 ◽

Vol 61 (16) ◽

pp. 5406-5413 ◽

Author(s):

Oswy Z. Pereira ◽

Tak-Hang Chan

Keyword(s):

Conjugate Addition ◽

Addition Reactions

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Conjugate Addition Reactions of Functionalized Organozinc and Copper Reagents to (2-Propynylidene)morpholinium Triflates

Synthesis ◽

10.1055/s-1995-4024 ◽

1995 ◽

Vol 1995 (08) ◽

pp. 957-963 ◽

Author(s):

Martina Brunner ◽

Gerhard Maas

Keyword(s):

Conjugate Addition ◽

Addition Reactions

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Stereoselective aldol and conjugate addition reactions mediated by proline‐based catalysts and its analogues: A concise review

European Journal of Organic Chemistry ◽

10.1002/ejoc.202100945 ◽

2021 ◽

Author(s):

Nagula Shankaraiah ◽

Durgesh Gurukkala Valapil ◽

Manasa Kadagathur

Keyword(s):

Conjugate Addition ◽

Addition Reactions ◽

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