Stereoselective synthesis of (2R,3R,4R)-3-hydroxy-2,4,6-trimethylheptanoic acid and determination of the absolute stereochemistry of the natural product from callipeltin A
- 5 July 2002
- journal article
- research article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 13 (12) , 1237-1239
- https://doi.org/10.1016/s0957-4166(02)00328-2
Abstract
No abstract availableKeywords
This publication has 3 references indexed in Scilit:
- Synthetic studies on callipeltin A: stereoselective synthesis of (2R,3R,4S)-3-hydroxy-2,4,6-trimethylheptanoic acidTetrahedron: Asymmetry, 2002
- Callipeltin A, an Anti-HIV Cyclic Depsipeptide from the New Caledonian Lithistida Sponge Callipelta sp.Journal of the American Chemical Society, 1996
- Chiral synthesis via organoboranes. 21. Allyl- and crotylboration of .alpha.-chiral aldehydes with diisopinocampheylboron as the chiral auxiliaryThe Journal of Organic Chemistry, 1989