Enantioselective synthesis of γ-lactones from thioglycolic acid: Syntheses of (−)-muricatacin and 5-epi-(−)-muricatacin
- 1 February 1998
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 9 (3) , 521-529
- https://doi.org/10.1016/s0957-4166(98)00007-x
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Synthesis of (4R,5R)-muricatacin and its (4R,5S)-analog by sequential use of the photo-induced rearrangement of epoxy diazomethyl ketonesTetrahedron, 1995
- Asymmetric synthesis of allylic sulfones useful as asymmetric building blocks.Journal of the American Chemical Society, 1995
- Enantiospecific synthesis of D-daunosamine from thioglycolic acidTetrahedron: Asymmetry, 1994
- Synthesis of (-)-Muricatacin and (-)-(5R,6S)-6-acetoxy-5-hexadecanolide, the Mosquito oviposition attractant pheromone, from D-isoascorbic acidTetrahedron Letters, 1994
- Muricatacin: A simple biologically active acetogenin derivative from the seeds of annona muricata (annonaceae)Tetrahedron Letters, 1991
- Synthesis of optically active α-alkylthioglycolic acid derivativesTetrahedron Letters, 1990
- Sulfoxide-mediated intramolecular hydroxylation of a remote olefin in an acyclic systemJournal of the American Chemical Society, 1984