Synthesis of (−)-bullatacin: The enantiomer of a potent, antitumor, 4-hydroxylated, Annonaceous acetogenin
- 6 August 1993
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 34 (32) , 5043-5046
- https://doi.org/10.1016/s0040-4039(00)60671-8
Abstract
No abstract availableThis publication has 23 references indexed in Scilit:
- Redox-controlled Bergman cycloaromatizations. Designed enediynes with DNA-cleaving properties and antitumor activityJournal of the American Chemical Society, 1992
- The NADH:ubiquinone oxidoreductase (complex I) of respiratory chainsQuarterly Reviews of Biophysics, 1992
- Stereoselective Synthesis of the Cytotoxic Acetogenins (+)- and (-)-MuricatacinSynlett, 1992
- Enantiomeric cholesterol as a probe of ion-channel structureJournal of the American Chemical Society, 1992
- Stereoselective Synthesis of the trans 2,4-Disubstituted Butyrolactone Moiety of Annonaceous AcetogeninsSynlett, 1992
- Synthesis of 1,3-Diynes Using Palladium-Copper CatalysisSynthetic Communications, 1991
- Molecular mode of action of annoninsPesticide Science, 1991
- Acetylcyclopropane as a five–carbon building block in the synthesis of some acetogenin insect pheromonesJournal of the Chemical Society, Perkin Transactions 1, 1991
- Bullatacin, Bullatacinone, and Squamone, a New Bioactive Acetogenin, from the Bark of Annona squamosaJournal of Natural Products, 1990
- Total synthesis of polyether antibiotics. Synthesis of the enantiomer of lasalocid A (X-537A)The Journal of Organic Chemistry, 1983