Enantioselective synthesis of a key tricyclic intermediateen route to (+)-gelsemine
- 6 August 1999
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 40 (32) , 5919-5922
- https://doi.org/10.1016/s0040-4039(99)01132-6
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Toward a potential total synthesis of gelsemine: A regioselective hydroboration directed by a remote olefinTetrahedron Letters, 1998
- Free Radical Cyclizations in Alkaloid Total Synthesis: (±)-21-Oxogelsemine and (±)-GelsemineJournal of the American Chemical Society, 1997
- Stereocontrolled Total Synthesis of (±)-GelsemineJournal of the American Chemical Society, 1996
- Total Synthesis of dL-21-OxogelsemineJournal of the American Chemical Society, 1994
- The total synthesis of (±)-gelsemineJournal of the Chemical Society, Chemical Communications, 1994
- A total synthesis of gelsemine: oxindole spiroannelationJournal of the Chemical Society, Chemical Communications, 1994
- Reaction of Na2Fe(CO)4 with an unsaturated aziridinium ion. Unprecedented rearrangement of an alkyltetracarbonylferrate intermediateThe Journal of Organic Chemistry, 1992
- Recent progress in the chemistry of indole alkaloids and mould metabolitesNatural Product Reports, 1992
- A new oxindole synthesisJournal of the Chemical Society, Perkin Transactions 1, 1991
- An approach to gelsemineTetrahedron Letters, 1987