(Q63344119)

English

A new approach to the stereoselective synthesis of conveniently protected α-allyl substituted amino acids; chiral key compounds in the synthesis of constrained peptide isostere constituents

article by Ramón Badorrey et al published January 1997 in Tetrahedron: Asymmetry

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scholarly article

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A new approach to the stereoselective synthesis of conveniently protected α-allyl substituted amino acids; chiral key compounds in the synthesis of constrained peptide isostere constituents (English)

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stereoselectivity

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inferred from title

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María D. Díaz-de-Villegas

object named as

Maria D. Díaz-de-Villegas

3

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author name string

Ramón Badorrey

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Carlos Cativiela

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JoséA. Gálvez

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Yolanda Lapeña

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publication date

January 1997

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Tetrahedron: Asymmetry

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8

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2

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311-317

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Conformationally constrained renin inhibitory peptides: gamma-lactam-bridged dipeptide isostere as conformational restriction

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Enantiomerically Enriched α-Methyl Amino Acids. Use of an Acyclic, Chiral Alanine-Derived Dianion with a High Diastereofacial Bias.†.

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Synthesis of (R)- and (S)-2-amino-2-methylbutanoic acid (Iva) in enantiomerically pure form

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New approaches to the asymmetric synthesis of α-methylphenylalanine

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Asymmetric synthesis of 3,3-diphenyl-2-methylalanine, a new unusual α-amino acid for peptides of biological interest

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Chiral 2-cyano esters as synthetic intermediates in the synthesis of R and S α-methylvaline

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Asymmetric Synthesis of .beta.-Lactams. Highly Diastereoselective Alkylation of Chiral 2-Cyano Esters

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Chiral 2-Cyanocinnamates in Conjugate Addition Asymmetric Enolate Trapping Reactions

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10.1016/S0957-4166(96)00516-2

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