Novel open‐chain and cyclic conformationally constrained (R)‐ and (S)‐α,α‐disubstituted tyrosine analogues
- 20 September 1995
- journal article
- research article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 78 (6) , 1567-1587
- https://doi.org/10.1002/hlca.19950780613
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- L‐Phenylalanine Cyclohexylamide: A simple and convenient auxiliary for the synthesis of optically pure α,α‐disubstituted (R)‐ and (S)‐amino acidsHelvetica Chimica Acta, 1995
- Three protein kinase structures define a common motifStructure, 1994
- Regulation of src family tyrosine kinases in lymphocytesTrends in Biochemical Sciences, 1993
- Recognition of a high-affinity phosphotyrosyl peptide by the Src homology-2 domain of p56lckNature, 1993
- Protein kinases: coming of ageCurrent Opinion in Structural Biology, 1992
- A New General Approach to Enantiomerically Pure Cyclic and Open‐Chain (R)‐ and (S)‐α,α‐Disubstituted α‐Amino AcidsHelvetica Chimica Acta, 1992
- Crystal structure of the phosphotyrosine recognition domain SH2 of v-src complexed with tyrosine-phosphorylated peptidesNature, 1992
- Mechanisms of biological control by phosphorylationCurrent Opinion in Structural Biology, 1991
- Structural versatility of peptides from Cα,αdialkylated glycines: Linear Ac3c homo‐oligopeptidesBiopolymers, 1989
- Stereochemistry of peptides containing 1‐aminocyclopentanecarboxylic acid (Acc5): Solution and solid‐state conformations of Boc‐Acc5‐Acc5‐NHMeBiopolymers, 1986