Asymmetric Synthesis of Phorboxazole B—Part I: Synthesis of the C20–C38 and C39–C46 Subunits
- 17 July 2000
- journal article
- Published by Wiley in Angewandte Chemie
- Vol. 112 (14) , 2633-2636
- https://doi.org/10.1002/1521-3757(20000717)112:14<2633::aid-ange2633>3.0.co;2-#
Abstract
No abstract availableThis publication has 50 references indexed in Scilit:
- Synthesis of the C22−C26 Tetrahydropyran Segment of Phorboxazole by a Stereoselective Prins CyclizationOrganic Letters, 2000
- Synthetic studies towards phorboxazole A. Stereoselective synthesis of the C3–C19 bis-oxane oxazole portion of the phorboxazole macrolideTetrahedron Letters, 2000
- Palladium-Catalyzed Cross-Coupling of Terminal Alkynes with 4-Trifloyloxazole: Studies toward the Construction of the C26−C31 Subunit of Phorboxazole AOrganic Letters, 2000
- Structure-Activity Investigations of Analogues of the C15-C26 Phorboxazoles SegmentSynlett, 1999
- Phorboxazole Synthetic Studies. 1. Construction of a C(3−19) Subtarget Exploiting an Extension of the Petasis−Ferrier RearrangementOrganic Letters, 1999
- Phorboxazole Synthetic Studies. 2. Construction of a C(20−28) Subtarget, a Further Extension of the Petasis−Ferrier RearrangementOrganic Letters, 1999
- Synthesis of the enantiopure C15–C26 segment of phorboxazole A and BTetrahedron Letters, 1999
- Absolute configuration of phorboxazoles A and B from the marine sponge, Phorbas sp. 2. C43 and complete stereochemistryTetrahedron Letters, 1996
- Absolute Configuration of Phorboxazoles A and B from the Marine Sponge Phorbas sp. 1. Macrolide and Hemiketal RingsJournal of the American Chemical Society, 1996
- Phorboxazoles A and B: potent cytostatic macrolides from marine sponge Phorbas speciesJournal of the American Chemical Society, 1995