Reversal of the phenylseleno- and phenylsulpheno-cyclizations. Synthesis of olefins from phenylseleno- and phenylsulpheno-lactones, phenylselenoethers, and α-hydroxyselenides
- 1 January 1979
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 2,p. 83-85
- https://doi.org/10.1039/c39790000083
Abstract
Sodium in liquid ammonia reacts with phenylseleno- and phenylsulpheno-lactones, phenylselenoethers, and α-silyloxyselenides to give olefinic products in good to excellent yields.This publication has 2 references indexed in Scilit:
- Synthesis and Biological Properties of Prostaglandin Endoperoxides, Thromboxanes and ProstacyclinsAngewandte Chemie International Edition in English, 1978
- Synthesis of (4E)-9-deoxy-6,9α-epoxy-Δ4-PGF1α, a prostacyclin (PGX) isomerJournal of the Chemical Society, Chemical Communications, 1977