Asymmetric syntheses of 3-amino-2-methylpentanoic acids. Configurations of the β-amino acid in majusculamide C, 57-normajusculamide C and dolastatins 11 and 12
Author:
Publisher
Elsevier BV
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis
Reference8 articles.
1. Structure of majusculamide C, a cyclic depsipeptide from Lyngbya majuscula
2. 57-Normajusculamide C, a Minor Cyclic Depsipeptide Isolated from Lyngbya majuscula
3. Isolation and Structure of the Cell Growth Inhibitory Depsipeptides Dolastatins 11 and 12
4. Enantiomeric Z- and E-crotyldiisopinocampheylboranes. Synthesis in high optical purity of all four possible stereoisomers of .beta.-methylhomoallyl alcohols
5. Direct, highly efficient synthesis from (S)-(+)-phenylglycine of the taxol and taxotere side chains
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1. ChemInform Abstract: Asymmetric Syntheses of 3-Amino-2-methylpentanoic Acids. Configurations of the β-Amino Acid in Majusculamide C, 57- Normajusculamide C and Dolastatins 11 and 12.;ChemInform;2010-08-20
2. Allylboration of Carbonyl Compounds;Organic Reactions;2009-04-15
3. Novel silyl-mediated 10-TMS-9-BBD organoborane reagents for asymmetric synthesis;Special Publications;2007
4. C2-Symmetric nitroxides and their potential as enantioselective oxidants;Tetrahedron: Asymmetry;2005-10
5. The Dolastatins;Anticancer Agents from Natural Products;2005-06-13
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