Enantioselective synthesis of a halichondrin B C(20)→C(36) precursor
- 25 September 1995
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 36 (39) , 7023-7026
- https://doi.org/10.1016/0040-4039(95)01454-p
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- An expeditious synthesis of the C(1)-C(14) subunit of halichondrin BTetrahedron Letters, 1994
- Isohomohalichondrin B, a new antitumour polyether macrolide from the New Zealand deep-water sponge Lissodendoryx sp.Tetrahedron Letters, 1994
- : Isolation and structure of halistatin 1 from the eastern Indian Ocean marine sponge Phakellia carteriThe Journal of Organic Chemistry, 1993
- Interaction of halichondrin B and homohalichondrin B with bovine brain tubulinBiochemical Pharmacology, 1993
- Natural products which interact with tubulin in the vinca domain: Maytansine, rhizoxin, phomopsin a, dolastatins 10 and 15 and halichondrin BPharmacology & Therapeutics, 1992
- Antineoplastic agents. 219. Isolation and structure of the cell growth inhibitory constituents from the western Pacific marine sponge Axinella spJournal of Medicinal Chemistry, 1991
- Synthesis of a C(22)a˚C(34) halichondrin precursor via a double dioxanone-to-dihydropyran rearrangementTetrahedron Letters, 1991
- Total synthesis of halichondrins: Enantioselective construction of a homochiral pentacyclic C1-C15 intermediate from d-riboseTetrahedron Letters, 1990
- Total synthesis of halichondrins: Highly stereoselective construction of a homochiral pentasubstituted H-ring pyran intermediate from α-d-glucoseTetrahedron Letters, 1989
- Halichondrins - antitumor polyether macrolides from a marine spongePure and Applied Chemistry, 1986