Application of the β-azidonation reaction to the synthesis of the antitumor alkaloid (+)-pancratistatin
- 1 December 1998
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 54 (51) , 15509-15524
- https://doi.org/10.1016/s0040-4020(98)00975-2
Abstract
No abstract availableThis publication has 29 references indexed in Scilit:
- A convergent synthesis of (+)-pancratistatin based on intramolecular electrophilic aromatic substitutionTetrahedron, 1997
- 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
- Asymmetric Total Synthesis of (+)-7-DeoxypancratistatinSynlett, 1995
- Asymmetric Total Synthesis of (+)-PancratistatinJournal of the American Chemical Society, 1995
- First Total Synthesis of (+)-Pancratistatin: An Unusual Set of ProblemsJournal of the American Chemical Society, 1995
- Synthesis of 10b-R-hydroxy-pancratistatin via narciclasineJournal of the Chemical Society, Chemical Communications, 1994
- 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
- Allylic and propargylic imidic esters in organic synthesisAccounts of Chemical Research, 1980