Synthetic studies of didemnins. II. Approaches to statine diastereomers
- 31 December 1987
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 28 (25) , 2837-2840
- https://doi.org/10.1016/s0040-4039(00)96222-1
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Renin inhibitors. Syntheses of subnanomolar, competitive, transition-state analog inhibitors containing a novel analog of statineJournal of Medicinal Chemistry, 1985
- Asymmetric reduction of prochiral 3-aryl-3-oxoesters with lithium borohydride using N,N′-dibenzoylcystine as a chiral auxiliaryJournal of the Chemical Society, Chemical Communications, 1985
- Stereoselective reduction of .ALPHA.-methyl-.BETA.-hydroxy ketones with zinc borohydride.CHEMICAL & PHARMACEUTICAL BULLETIN, 1984
- Cram rule selectivity in the Lewis acid catalyzed cyclocondensation of chiral aldehydes. A convenient route to chiral systems of biological interestThe Journal of Organic Chemistry, 1982
- Stereoselective Synthesis of Diastereomeric Amino Alcohols from Chiral Aminocarbonyl Compounds by Reduction or by Addition of Organometallic ReagentsSynthesis, 1982
- Didemnins: Antiviral and Antitumor Depsipeptides from a Caribbean TunicateScience, 1981
- Synthesis of all the stereoisomers of statine (4-amino-3-hydroxy-6-methylheptanoic acid). Inhibition of pepsin activity by N-carbobenzoxy-L-valyl-L-valyl-statine derived from the four stereoisomersJournal of Medicinal Chemistry, 1979
- Synthesis of 4-amino-3-hydroxy-6-methylheptanoic acid by a modified Reformatsky reactionThe Journal of Organic Chemistry, 1978
- The Stereoselective Synthesis of threo-3-Hydroxy-4-amino AcidsBulletin of the Chemical Society of Japan, 1976
- Synthesis of (3S, 4S)- and (3S, 4R)-4-Amino-3-hydroxy-6-methylheptanoic Acid, and Their N-(Acetyl-l-valyl-l-valyl) DerivativesBulletin of the Chemical Society of Japan, 1975