Alkoxycarbonylation and selective deprotection of N-silyl derivatives of L-arginine
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. An acid labile arginine derivative for peptide synthesis: NG-2,2,5,7,8-pentamethylchroman-6-sulphonyl-L-arginine
2. A specific inhibitor of nitric oxide formation from l-arginine attenuates endothelium-dependent relaxation
3. Nitric oxide synthase structure and mechanism
4. A one-pot N-protection of L-arginine.
5. Synthesis and biological activity of the novel nitric oxide synthase inhibitor Nω′-hydroxy-Nω-methyl-L-arginine
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1. ChemInform Abstract: Alkoxycarbonylation and Selective Deprotection of N-Silyl Derivatives of L-Arginine.;ChemInform;2010-06-20
2. Studies on the preparation and crystal polymorphism of 2-acetamidobenzamide and related compounds;Arkivoc;2007-12-19
3. Alkylboron and -silicon Compounds;Comprehensive Organic Functional Group Transformations II;2005
4. New tris-alkoxycarbonyl arginine derivatives for peptide synthesis;Journal of Peptide Science;2004
5. Synthesis and absolute configuration of Stellettadine A;Bioorganic & Medicinal Chemistry Letters;2001-06
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