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
- 31 January 1993
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 4 (1) , 69-72
- https://doi.org/10.1016/s0957-4166(00)86016-4
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Direct, highly efficient synthesis from (S)-(+)-phenylglycine of the taxol and taxotere side chainsThe Journal of Organic Chemistry, 1991
- Enantiomeric 3,7-Dimethylocta-1,7-dienes as Useful Chiral Building Blocks. A New Access to Both Optical Antipodes of Natural (E)-3,7-Dimethyloct-2-ene-1,8-diol and (E)-3,7-Dimethyloct-2-ene-1,8-dicarboxylic AcidHelvetica Chimica Acta, 1990
- Isolation and Structure of the Cell Growth Inhibitory Depsipeptides Dolastatins 11 and 12HETEROCYCLES, 1989
- 57-Normajusculamide C, a Minor Cyclic Depsipeptide Isolated from Lyngbya majusculaJournal of Natural Products, 1988
- Enantiomeric Z- and E-crotyldiisopinocampheylboranes. Synthesis in high optical purity of all four possible stereoisomers of .beta.-methylhomoallyl alcoholsJournal of the American Chemical Society, 1986
- Structure of majusculamide C, a cyclic depsipeptide from Lyngbya majusculaThe Journal of Organic Chemistry, 1984