First total synthesis of (+)-allopumiliotoxin 339A. A practical entry to dendrobatid alkaloids of the allopumiliotoxin class
- 1 January 1992
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 114 (1) , 368-369
- https://doi.org/10.1021/ja00027a061
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Pumiliotoxin alkaloids: A new class of sodium channel agentsBiochemical Pharmacology, 1990
- The total synthesis of the polyether antibiotic X-206Journal of the American Chemical Society, 1988
- Pumiliotoxin B binds to a site on the voltage-dependent sodium channel that is allosterically coupled to other binding sites.Proceedings of the National Academy of Sciences, 1988
- Pumiliotoxin alkaloids: relationship of cardiotonic activity to sodium channel activity and phosphatidylinositol turnoverJournal of Medicinal Chemistry, 1988
- Cardiotonic activities of pumiliotoxin B, pyrethroids and a phorbol ester and their relationships with phosphatidylinositol turnoverBiochimica et Biophysica Acta (BBA) - Molecular Cell Research, 1987
- A new class of cardiotonic agents: structure-activity correlations for natural and synthetic analogs of the alkaloid pumiliotoxin B (8-hydroxy-8-methyl-6-alkylidene-1-azabicyclo[4.3.0]nonanes)Journal of Medicinal Chemistry, 1985
- Enantioselective total syntheses of pumiliotoxin B and pumiliotoxin 251D. A general entry to the pumiliotoxin A alkaloids via stereospecific iminium ion-vinylsilane cyclizationsJournal of the American Chemical Society, 1984
- Oxidation of long-chain and related alcohols to carbonyls by dimethyl sulfoxide "activated" by oxalyl chlorideThe Journal of Organic Chemistry, 1978