Absolute Stereochemistry of Amphidinolides G and H
- 8 August 2000
- journal article
- letter
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 2 (18) , 2805-2807
- https://doi.org/10.1021/ol006223b
Abstract
Absolute stereochemistry of amphidinolides G (1) and H (2), potent cytotoxic 27- and 26-membered macrolides, respectively, isolated from a marine dinoflagellate Amphidinium sp., was determined by X-ray diffraction analysis, synthesis of a degradation product (3) of 2, and interconversion between 1 and 2.Keywords
This publication has 5 references indexed in Scilit:
- Amphidinolide T, Novel 19-Membered Macrolide from Marine Dinoflagellate Amphidinium sp.The Journal of Organic Chemistry, 2000
- Amphidinolide V, novel 14-membered macrolide from marine dinoflagellate Amphidinium sp.Tetrahedron Letters, 2000
- Absolute stereochemistry of amphidinolide BTetrahedron Letters, 1994
- The Structures of Amphidinolide B Isomers: Strongly Cytotoxic Macrolides Produced by a Free-Swimming Dinoflagellate, Amphidinium spJournal of the American Chemical Society, 1994
- Regioselective synthesis of 1-formylcyclohexenes by one-carbon homologationThe Journal of Organic Chemistry, 1991