Diastereoselective deuteration of (Z)-α,β-dehydrotryptophanyl-containing biological peptides controlled by chiral rhodium catalysts
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference19 articles.
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3. Asymmetric deuteration of N-acetyl-(Z)-α,β-dehydrotryptophan-(L)-phenylalanine methyl ester produced by (L)-tryptophan 2′,3′-oxidase from Chromobacterium violaceum. A new route for stereospecific labelling of peptides
4. Proton and tritium nmr relaxation studies of peptide inhibitor binding to bacterial collagenase: Conformation and dynamics
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1. ChemInform Abstract: Diastereoselective Deuteration of (Z)-α,β-Dehydrotryptophanyl-Containing Biological Peptides Controlled by Chiral Rhodium Catalysts.;ChemInform;2010-06-20
2. NMR Confirmation That Tryptophan Dehydrogenation Occurs with Syn Stereochemistry during the Biosynthesis of CDA in Streptomyces coelicolor;The Journal of Organic Chemistry;2007-10-11
3. Stereochemical Course of Tryptophan Dehydrogenation during Biosynthesis of the Calcium-Dependent Lipopeptide Antibiotics;Organic Letters;2007-03-14
4. Animal experimentation in snake venom research and in vitro alternatives;Toxicon;2003-08
5. Photochemistry of cyclopropanes, methylenecyclopropanes, and vinylidenecyclopropanes;Journal of Photochemistry and Photobiology C: Photochemistry Reviews;2000-12
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