Substituent-directed oxidation: a simple preparation of γ and δ-lactones by oxidative cyclization of hydroxyalkenes.
- 31 December 1985
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 26 (2) , 127-130
- https://doi.org/10.1016/s0040-4039(00)61860-9
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- A facile entry to bicyclic γ-lactones and a short synthesis of (±)-dihydroactinidiolideTetrahedron Letters, 1984
- An analysis of the diastereomeric transition state interactions for stereoselective epoxidation of acyclic allylic alcohols with peroxy-acidsTetrahedron Letters, 1981
- Further studies on stereospecific epoxidation of allylic alcohols Iltifat HasanTetrahedron Letters, 1980
- The first practical method for asymmetric epoxidationJournal of the American Chemical Society, 1980
- Cooperative effect by a hydroxy and ether oxygen in epoxidation with a peracidTetrahedron Letters, 1979
- Chromyl chloride oxidations of olefins. Possible role of organometallic intermediates in the oxidations of olefins by oxo transition metal speciesJournal of the American Chemical Society, 1977