Application of a set-induced photospirocyclization methodology to harringtonine ring construction
- 31 December 1989
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 30 (32) , 4185-4188
- https://doi.org/10.1016/s0040-4039(01)80685-7
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Total syntheses of (.+-.)-cephalotaxine and (.+-.)-8-oxocephalotaxineThe Journal of Organic Chemistry, 1988
- Synthesis via vinyl sulfones. 27. Total synthesis of cephalotaxine. The first example of an intramolecular [4 + 2] cycloaddition where the dienophile has been delivered from the face opposite to the tethering moietyJournal of the American Chemical Society, 1988
- Dual diradical and cation diradical cyclization mechanisms for silylalkenyl iminium salt. Electron-transfer induced photocyclization reactionsJournal of the American Chemical Society, 1987
- A photochemical route for erythrane ring constructionThe Journal of Organic Chemistry, 1987
- A novel and stereoselective synthesis of (±)-cephalotaxine and its analogueTetrahedron Letters, 1986
- Exploratory and mechanistic studies of the electron-transfer-initiated photoaddition reactions of allylsilane-iminium salt systemsThe Journal of Organic Chemistry, 1984
- Electron transfer initiated iminium salt photospirocyclization methodologies. Model studies for harringtonine alkaloid synthesisThe Journal of Organic Chemistry, 1982
- Total synthesis of the Cephalotaxus alkaloids. Problem in nucleophilic aromatic substitutionJournal of the American Chemical Society, 1975
- Antitumor Alkaloids from Cephalotaxus harringtonia: Structure and ActivityJournal of Pharmaceutical Sciences, 1972
- Structure of cephalotaxine and related alkaloidsTetrahedron Letters, 1969