Enantioselective synthesis of the 4-hydroxy buteneolide terminus of mucocin and related annonaceous acetogenins
- 1 December 1998
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 39 (52) , 9627-9628
- https://doi.org/10.1016/s0040-4039(98)02206-0
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Total Synthesis of Muconin by Efficient Assembly of Chiral Building BlocksThe Journal of Organic Chemistry, 1998
- Recent Developments in the Synthesis of Annonaceous AcetogeninsIsrael Journal of Chemistry, 1997
- Total synthesis of (+)-13,14-threo-densicomacinTetrahedron Letters, 1995
- Mucocin: A New Annonaceous Acetogenin Bearing a Tetrahydropyran RingJournal of the American Chemical Society, 1995
- Synthetic strategies to acetogenins. The hydroxybutenolide terminusTetrahedron Letters, 1995
- Total synthesis of the potent antitumor, bis-tetrahydrofuranyl annonaceous acetogenins (+)-asimicin and (+)-bullatacinTetrahedron Letters, 1995
- Stereostructural studies on the 4-hydroxylated annonaceous acetogenins: A novel use of Mosher ester data for determining relative configuration [between C(4) and C(36)]Tetrahedron Letters, 1994
- Total synthesis of (+)-rolliniastatin 1Tetrahedron Letters, 1994
- Catalytic asymmetric allylation of aldehydesJournal of the American Chemical Society, 1993
- Synthesis of .gamma.- and .delta.-lactones by free-radical annelation of Se-phenyl selenocarbonatesThe Journal of Organic Chemistry, 1992