Synthesis of C(3) Benzofuran-Derived Bisaryl Quaternary Centers: Approaches to Diazonamide A
- 4 October 2000
- journal article
- letter
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 2 (22) , 3521-3523
- https://doi.org/10.1021/ol006578v
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Progress toward Synthesis of Diazonamide A. Preparation of a 3-(Oxazol-5-yl)-4-trifluoromethylsulfonyloxyindole and Its Use in Biaryl Coupling ReactionsOrganic Letters, 2000
- Synthesis of the 4-arylindole portion of the antitumor agent diazonamide and related studiesTetrahedron Letters, 2000
- Synthesis of the dichlorobisoxazole-indole portion of the antitumor agent diazonamide by a putative biogenetic strategyTetrahedron Letters, 2000
- Macrocyclic Triarylethylenes via Heck Endocyclization: A System Relevant to Diazonamide SynthesisThe Journal of Organic Chemistry, 1998
- Synthetic Studies on Diazonamide A. Benzofuranone-Tyrosine and Indole-Oxazole Fragment Support StudiesSynlett, 1996
- Synthesis of heterocyclic natural products: Model studies towards diazonamide APublished by Walter de Gruyter GmbH ,1994
- A new diazoacylating reagent: preparation, structure, and use of succinimidyl diazoacetateThe Journal of Organic Chemistry, 1993
- Isolation and structure determination of diazonamides A and B, unusual cytotoxic metabolites from the marine ascidian Diazona chinensisJournal of the American Chemical Society, 1991
- Intramolecular cyclopropanation reaction of furanyl diazo ketonesThe Journal of Organic Chemistry, 1989
- The ortho-Claisen Rearrangement. IV. The Rearrangement of X-Cinnamyl p-Tolyl Ethers1Journal of the American Chemical Society, 1961