Synthesis of the Antitumor Alkaloid (+)-Pancratistatin Using the β-Azidonation Reaction via a Prochiral 4-Arylcyclohexanone Derivative
- 13 May 1998
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 120 (21) , 5341-5342
- https://doi.org/10.1021/ja980407s
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
- Toluene Dioxygenase-Mediated cis-Dihydroxylation of Aromatics in Enantioselective Synthesis. Asymmetric Total Syntheses of Pancratistatin and 7-Deoxypancratistatin, Promising Antitumor Agents1Journal of the American Chemical Society, 1996
- Hypervalent Iodine Chemistry: New Oxidation Reactions Using the Iodosylbenzene−Trimethylsilyl Azide Reagent Combination. Direct α- and β-Azido Functionalization of Triisopropylsilyl Enol EthersJournal of the American Chemical Society, 1996
- Asymmetric Total Synthesis of (+)-PancratistatinJournal of the American Chemical Society, 1995
- Lycoricidine and pancratistatin analogues from cyclopentadieneJournal of the Chemical Society, Perkin Transactions 1, 1994
- Synthesis of 10b-R-hydroxy-pancratistatin via narciclasineJournal of the Chemical Society, Chemical Communications, 1994
- First Synthesis of Cotarnone, the Key Intermediate for the Synthesis of CotarnineSynthetic Communications, 1990
- New trialkylsilyl enol ether chemistry. Regiospecific and stereospecific sequential electrophilic additionJournal of the American Chemical Society, 1990
- Total synthesis of (.+-.)-pancratistatinJournal of the American Chemical Society, 1989
- Antineoplastic Agents, 120. Pancratium littoraleJournal of Natural Products, 1986
- Isolation and structure of pancratistatinJournal of the Chemical Society, Chemical Communications, 1984