An improved synthesis of N-aryl-hydantoin LFA-1 antagonists via the enantiospecific alkylation of an isobutyraldehyde-derived imidazolidinone template-Reference-Cited by-同舟云学术

An improved synthesis of N-aryl-hydantoin LFA-1 antagonists via the enantiospecific alkylation of an isobutyraldehyde-derived imidazolidinone template

Published:2001-02 Issue:1 Volume:12 Page:101-104
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Frutos Rogelio P.,Stehle Sandra,Nummy Laurence,Yee Nathan

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference11 articles.

1. Synthesis of protected, chiral α,α-disubstituted α-amino acids via a Beckmann rearrangement

2. Enantioselective Synthesis of α,α-Disubstituted Amino Acid Derivatives via Enzymatic Resolution: Preparation of a Thiazolyl-Substituted α-Methyl α-Benzyl Amine

3. Stereoselective synthesis of quaternary α-amino acids. Part 1: Acyclic compounds

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