A biomimetic approach to the synthesis of rocaglamide based on a photochemical [2+2] cycloaddition of a cinnamate unit to a flavone.
- 13 August 1993
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 34 (33) , 5313-5316
- https://doi.org/10.1016/s0040-4039(00)73983-9
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Synthesis of the novel anti-leukaemic tetrahydrocyclopenta[b]benzofuran, rocaglamide and related synthetic studiesJournal of the Chemical Society, Perkin Transactions 1, 1992
- Lewis acid catalysis of photochemical reactions. 7. Photodimerization and cross-cycloaddition of cinnamic estersJournal of the American Chemical Society, 1988
- Regioselective photodimerization of cinnamic acid in a micellar solutionJournal of the Chemical Society, Chemical Communications, 1988
- Organic photochemistry in organized mediaTetrahedron, 1986
- Photodimerization of Lewis acid complexes of cinnamate esters in solution and the solid stateJournal of the American Chemical Society, 1984
- X-Ray crystal structure of rocaglamide, a novel antileulemic 1H-cyclopenta[b]benzofuran from Aglaia elliptifoliaJournal of the Chemical Society, Chemical Communications, 1982
- Photocycloaddition of coumarin to tetramethylethylene. Photoreaction associated with the apparent interception of the coumarin singlet excimerJournal of the American Chemical Society, 1975