Asymmetric cis - Hydroxylation via Epoxidation-Carboxylation: A Formal Synthesis of (+)-Citreoviral
- 31 December 1987
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 28 (4) , 375-378
- https://doi.org/10.1016/s0040-4039(00)95732-0
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Procedure for the catalytic asymmetric epoxidation of allylic alcohols in the presence of molecular sievesThe Journal of Organic Chemistry, 1986
- Total synthesis and the absolute configuration of citreoviral and citreoviridinTetrahedron Letters, 1985
- Palladium-mediated vicinal cleavage of allyl epoxides with retention of stereochemistry: a cis hydroxylation equivalentJournal of the American Chemical Society, 1985
- PALLADIUM CATALYZED REACTION OF BUTADIENE MONOXIDE WITH CARBON DIOXIDEChemistry Letters, 1985
- Natural polyene α-pyrones. Synthesis of (±)-citreoviralTetrahedron Letters, 1985
- Hrydroxyl-directed iodoetherifications of allylic alcohols. Synthesis of (±)-citreoviral.Tetrahedron Letters, 1985
- Total synthesis of (±)-citreoviralJournal of the Chemical Society, Chemical Communications, 1985
- Isolation and stereostructures of citreoviral, citreodiol, and epicitreodiolTetrahedron Letters, 1984
- Structure of citreoviridin, a mycotoxin produced by penicillium citreo-viride molded on riceTetrahedron, 1977