Total Synthesis and Absolute Configuration of the Novel Microtubule‐Stabilizing Agent Peloruside A
Open Access
- 10 April 2003
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 42 (14), 1648-1652
- https://doi.org/10.1002/anie.200351145
Abstract
No abstract availableThis publication has 24 references indexed in Scilit:
- Dimethylmalonyltrialkylphosphoranes: New General Reagents for Esterification Reactions Allowing Controlled Inversion or Retention of Configuration on Chiral AlcoholsThe Journal of Organic Chemistry, 2003
- An Approach to the Stereoselective Synthesis of syn- and anti-1,3-Diol Derivatives. Retention of Configuration in the Mitsunobu ReactionThe Journal of Organic Chemistry, 2002
- Total Synthesis of (+)-Phorboxazole A Exploiting the Petasis−Ferrier RearrangementJournal of the American Chemical Society, 2001
- Synthesis of Functionalized Olefins by Cross and Ring-Closing MetathesesJournal of the American Chemical Society, 2000
- Peloruside A: A Potent Cytotoxic Macrolide Isolated from the New Zealand Marine Sponge Mycale sp.The Journal of Organic Chemistry, 1999
- Total Synthesis of Bryostatin 2Journal of the American Chemical Society, 1999
- Synthesis of the First Members of a New Class of Biologically Active Bryostatin AnaloguesJournal of the American Chemical Society, 1998
- A Stereochemical Model for Merged 1,2- and 1,3-Asymmetric Induction in Diastereoselective Mukaiyama Aldol Addition Reactions and Related ProcessesJournal of the American Chemical Society, 1996
- The mechanism of the Mitsunobu esterification reaction. Part II. The involvement of (acyloxy)alkoxyphosphoranesThe Journal of Organic Chemistry, 1989
- Chiral synthesis via organoboranes. 13. A highly diastereoselective and enantioselective addition of [(Z)-.gamma.-alkoxyallyl]diisopinocampheylboranes to aldehydesJournal of the American Chemical Society, 1988