Synthesis of octalactin lactone and side chain
- 1 July 1996
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 37 (29) , 5049-5052
- https://doi.org/10.1016/0040-4039(96)01014-3
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- A synthetic approach towards octalactin A, based on the stereoselective reduction of α,β-unsaturated ketonesTetrahedron Letters, 1995
- Medium ring lactonesTetrahedron, 1995
- Total Synthesis of (+)-Octalactins A and B: Unusual Metabolites from a Marine MicrobeJournal of the American Chemical Society, 1994
- Total Synthesis of Octalactin A and BJournal of the American Chemical Society, 1994
- Octalactins A and B: cytotoxic eight-membered-ring lactones from a marine bacterium, Streptomyces spJournal of the American Chemical Society, 1991
- Asymmetric synthesis using tartrate ester modified allylboronates. 1. Factors influencing stereoselectivityThe Journal of Organic Chemistry, 1990
- A convenient procedure for the monosilylation of symmetric 1,n-diolsThe Journal of Organic Chemistry, 1986
- 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
- Pyridinium chlorochromate. An efficient reagent for oxidation of primary and secondary alcohols to carbonyl compoundsTetrahedron Letters, 1975
- Control of the steric course of the Wittig reactionTetrahedron, 1963