Xanthic anhydrides: A novel and convenient source of alkoxythiocarbonyl and alkyl radicals.
- 1 September 1993
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 49 (36) , 8257-8266
- https://doi.org/10.1016/s0040-4020(01)88043-1
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- On the mechanism of deoxygenation of secondary alcohols by tin hydride reduction of methyl xanthates and other thiocarbonyl derivativesTetrahedron Letters, 1990
- Improved methods for the radical deoxygenation of secondary alcoholsTetrahedron Letters, 1989
- A novel radical chain reaction of xanthic anhydrides. Further observations on the intermediacy of alkoxy-thiocarbonyl radicals in the Barton-McCombie reactionTetrahedron Letters, 1989
- On the use of S-(4-alkenyl)-dithiocarbonates as mechanistic probes in the barton-McCombie radical deoxygenation reactionTetrahedron Letters, 1988
- On the mechanism of reductive degradation of dithiocarbonates by tributylstannaneJournal of the Chemical Society, Perkin Transactions 1, 1988
- On the mechanism of the deoxygenation of secondary alcohols by the reduction of their methyl xanthates by tin hydridesTetrahedron, 1986
- On the mechanism of reduction of dithiocarbonates (xanthates) with tributylstannaneJournal of the Chemical Society, Chemical Communications, 1985
- Nucleic acid related compounds. 42. A general procedure for the efficient deoxygenation of secondary alcohols. Regiospecific and stereoselective conversion of ribonucleosides to 2'-deoxynucleosidesJournal of the American Chemical Society, 1983
- Modern methods for the radical deoxygenation of alcoholsTetrahedron, 1983
- A new method for the deoxygenation of secondary alcoholsJournal of the Chemical Society, Perkin Transactions 1, 1975