ChemInform Abstract: Michael Addition Reactions Between Nucleophilic Glycine Equivalents and Acrylic Acid Derivatives as a Practical and Generalized Approach to the Asymmetric Synthesis of Î²-Substituted Î±-Amino Acids

Vadim A. Soloshonok; Hisanori Ueki; Trevor K. Ellis

doi:10.1002/chin.201001243

ChemInform Abstract: Michael Addition Reactions Between Nucleophilic Glycine Equivalents and Acrylic Acid Derivatives as a Practical and Generalized Approach to the Asymmetric Synthesis of Î²-Substituted Î±-Amino Acids

ChemInform ◽

10.1002/chin.201001243 ◽

2010 ◽

Vol 41 (1) ◽

pp. no-no

Author(s):

Vadim A. Soloshonok ◽

Hisanori Ueki ◽

Trevor K. Ellis

Keyword(s):

Amino Acids ◽

Acrylic Acid ◽

Asymmetric Synthesis ◽

Michael Addition ◽

Addition Reactions

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ChemInform Abstract: Asymmetric Synthesis of α-Amino Acids via Homologation of Ni(II) Complexes of Glycine Schiff Bases. Part 3. Michael Addition Reactions and Miscellaneous Transformations

ChemInform ◽

10.1002/chin.201442265 ◽

2014 ◽

Vol 45 (42) ◽

pp. no-no

Author(s):

Jose Luis Acena ◽

Alexander E. Sorochinsky ◽

Vadim Soloshonok

Keyword(s):

Amino Acids ◽

Asymmetric Synthesis ◽

Schiff Bases ◽

Michael Addition ◽

Addition Reactions

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Asymmetric synthesis of α-amino acids via homologation of Ni(II) complexes of glycine Schiff bases. Part 3: Michael addition reactions and miscellaneous transformations

Amino Acids ◽

10.1007/s00726-014-1764-5 ◽

2014 ◽

Vol 46 (9) ◽

pp. 2047-2073 ◽

Cited By ~ 83

Author(s):

José Luis Aceña ◽

Alexander E. Sorochinsky ◽

Vadim Soloshonok

Keyword(s):

Amino Acids ◽

Asymmetric Synthesis ◽

Schiff Bases ◽

Michael Addition ◽

Addition Reactions

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Amino Acids. XV. Michael Addition Reactions of Diethyl Acetamidomalonate1

Journal of the American Chemical Society ◽

10.1021/ja01576a035 ◽

1957 ◽

Vol 79 (19) ◽

pp. 5203-5205 ◽

Cited By ~ 10

Author(s):

George H. Cocolas ◽

Walter H. Hartung

Keyword(s):

Amino Acids ◽

Michael Addition ◽

Addition Reactions

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Asymmetric Synthesis of β-Amino Acids via the Michael Addition of Chiral Metal Amides

Journal of Synthetic Organic Chemistry Japan ◽

10.5059/yukigoseikyokaishi.55.26 ◽

1997 ◽

Vol 55 (1) ◽

pp. 26-34 ◽

Cited By ~ 16

Author(s):

Stephen G. DAVIES ◽

Osamu ICHIHARA

Keyword(s):

Amino Acids ◽

Asymmetric Synthesis ◽

Michael Addition ◽

Metal Amides ◽

The Michael Addition

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Asymmetric Synthesis of 3-Methylthio Alcohols by Intramolecular Michael Addition Reactions.

ChemInform ◽

10.1002/chin.200529077 ◽

2005 ◽

Vol 36 (29) ◽

pp. no-no

Author(s):

Aurelio Ortiz ◽

Hector Hernandez ◽

Guadalupe Mendoza ◽

Leticia Quintero ◽

Sylvain Bernes

Keyword(s):

Asymmetric Synthesis ◽

Michael Addition ◽

Addition Reactions

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ChemInform Abstract: Asymmetric Synthesis of α-Amino Acids via Homologation of Ni(II) Complexes of Glycine Schiff Bases. Part 2. Aldol, Mannich Addition Reactions, Deracemization and (S) to (R) Interconversion of α-Amino Acids

ChemInform ◽

10.1002/chin.201351246 ◽

2013 ◽

Vol 44 (51) ◽

pp. no-no

Author(s):

Alexander E. Sorochinsky ◽

Jose Luis Acena ◽

Hiroki Moriwaki ◽

Tatsunori Sato ◽

Vadim Soloshonok

Keyword(s):

Amino Acids ◽

Asymmetric Synthesis ◽

Schiff Bases ◽

Addition Reactions

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Highly Diastereoselective Michael Addition Reactions Between Nucleophilic Glycine Equivalents and β-Substituted α,β-Unsaturated Carboxylic Acid Derivatives: A General Approach to the Stereochemically Defined and Sterically χ-Constrained α-amino Acids

ChemInform ◽

10.1002/chin.200313247 ◽

2003 ◽

Vol 34 (13) ◽

Author(s):

Vadim A. Soloshonok

Keyword(s):

Amino Acids ◽

Carboxylic Acid ◽

Michael Addition ◽

Addition Reactions ◽

Unsaturated Carboxylic Acid

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Highly Diastereoselective Michael Addition Reactions between Nucleophilic Glycine Equivalents and β-substituted-α,β-Unsaturated Carboxylic acid Derivatives a General Approach to the Stereochemically Defined and Sterically χ-Constrained α-Amino Acids

Current Organic Chemistry ◽

10.2174/1385272024605014 ◽

2002 ◽

Vol 6 (4) ◽

pp. 341-364 ◽

Cited By ~ 71

Author(s):

Vadim Soloshonok

Keyword(s):

Amino Acids ◽

Carboxylic Acid ◽

Michael Addition ◽

Addition Reactions ◽

Unsaturated Carboxylic Acid

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ChemInform Abstract: Facile Asymmetric Synthesis of α-Amino Acids Employing Chiral Ligand Mediated Asymmetric Addition Reactions of Phenyllithium with Imines.

ChemInform ◽

10.1002/chin.200116193 ◽

2001 ◽

Vol 32 (16) ◽

pp. no-no

Author(s):

Masayoshi Hasegawa ◽

Daisuke Taniyama ◽

Kiyoshi Tomioka

Keyword(s):

Amino Acids ◽

Asymmetric Synthesis ◽

Addition Reactions ◽

Chiral Ligand ◽

Asymmetric Addition

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Asymmetric synthesis of 3-methylthio alcohols by intramolecular Michael addition reactions

Tetrahedron Letters ◽

10.1016/j.tetlet.2005.02.021 ◽

2005 ◽

Vol 46 (13) ◽

pp. 2243-2246 ◽

Cited By ~ 6

Author(s):

Aurelio Ortiz ◽

Hector Hernández ◽

Guadalupe Mendoza ◽

Leticia Quintero ◽

Sylvain Bernès

Keyword(s):

Asymmetric Synthesis ◽

Michael Addition ◽

Addition Reactions

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