Diastereoselective alkylation of sultam-derived amino acid aldimines preparation of Cα-methylated amino acids
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. Asymmetric alkylations of a sultam-derived glycinate equivalent: practical preparation of enantiomerically pure α-amino acids
2. Asymmetric synthesis of L-diphenylalanine and L-9-fluorenylglycine via room temperature alkylations of a sultam-derived glycine imine
3. Asymmetric synthesis of the diastereoisomers of L-1-indanylglycine and L-1-benz[f]indanylglycine, χ1,χ2-constrained side-chain derivatives of L-phenylalanine and L-2-naphthylalanine
4. Acidities of glycine Schiff bases and alkylation of their conjugate bases
5. ?-Alkylation of Amino Acids without Racemization. Preparation of Either (S)- or (R)-?-Methyldopa from (S)-Alanine
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3. ChemInform Abstract: Diastereoselective Alkylation of Sultam-Derived Amino Acid Aldimines. Preparation of Cα-Methylated Amino Acids.;ChemInform;2010-08-17
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