Statine and its derivatives. Conformational studies using nuclear magnetic resonance spectrometry and energy calculations
Author:
Publisher
Wiley
Subject
Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-3011.1983.tb02098.x/fullpdf
Reference16 articles.
1. PEPSTATIN, A NEW PEPSIN INHIBITOR PRODUCED BY AGTINOMYGETES
2. Didemnins: Antiviral and Antitumor Depsipeptides from a Caribbean Tunicate
3. SYNTHESIS OF 4-AMINO-3 HYDROXY-6-METHYLHEPTANOIG ACID, AN AMINE COMPONENT OF PEPSTATIN
4. X-RAY STRUCTURE DETERMINATION OF 4-AMINO-3-HYDROXY-6-METHYLHEPTANOIC ACID, AN AMINE COMPONENT OF PEPSTATIN
5. Synthesis of (3S,4S)-4-amino-3-hydroxy-6-methylheptanoic acid derivatives. Analysis of diastereomeric purity
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1. Conformational preferences and self-association modes of two diastereomeric statine derivatives;International Journal of Peptide and Protein Research;2009-01-12
2. A Simple Microscale Method for Determining the Relative Stereochemistry of Statine Units;The Journal of Organic Chemistry;2008-11-07
3. Quantum mechanical modeling of aspartic proteinase interactions: Difference in binding of diastereomeric statine models;Biochemical and Biophysical Research Communications;1988-12
4. Asymmetric Synthesis via Acetal Templates. 14.1 Preparation of Enantiomerically Pure (3S,4S)- and (3S,4R)-Statine Derivatives;Tetrahedron Letters;1987
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