Thionyl chloride/triethylamine : a powerful reagent for regiospecific and stereospecific formation of olefins from β-hydroxyselenides : stereospecific deoxygenation of di- and trisubstituted epoxides a [C.C] connective route to di-, tri- and tetrasubstituted olefins.
- 31 October 1976
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 17 (41) , 3743-3746
- https://doi.org/10.1016/s0040-4039(00)93098-3
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- New regiospecific routes to olefins from β-hydroxy selenidesTetrahedron Letters, 1976
- Regiospecific synthesis of αβ-unsaturated epoxidesTetrahedron Letters, 1976
- The preparation of seleniranium and selenirenium ionsTetrahedron Letters, 1975
- Selenium stablized anions. Conversion of β-hydroxy selenides into olefinsJournal of the Chemical Society, Chemical Communications, 1975
- A new method for the synthesis of olefins via β-hydroxyalkyl phenyl sulfidesTetrahedron Letters, 1972