A new synthesis of allylic alcohols or their derivatives via reductive elimination from γ-phenylthio-β-nitroalcohols with tributyltinhydride
- 31 December 1984
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 25 (46) , 5319-5322
- https://doi.org/10.1016/s0040-4039(01)81593-8
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- The Michael reaction of silyl enol ethers or ketene silyl acetals with conjugated nitro olefins activated by Lewis acids: new synthesis of 1,4-diketones and .gamma.-oxo estersJournal of the American Chemical Society, 1984
- 2′‐Nitro‐2′‐propen‐1′‐yl 2,2‐Dimethylpropanoate (NPP), A Multiple Coupling ReagentHelvetica Chimica Acta, 1984
- A convenient preparation of conjugated nitro olefins by electrochemical methodTetrahedron Letters, 1983
- FREE RADICAL CHAIN ELIMINATION REACTION (ERC1). CONVERSION OF VICINAL DINITRO COMPOUNDS OR β-NITRO SULFONES TO OLEFINS WITH TRIBUTYLTIN HYDRIDEChemistry Letters, 1981
- Stereochemistry of free-radical eliminations on .beta.-phenylsulfonyl radicalsThe Journal of Organic Chemistry, 1980
- The stereochemistry of free radical eliminations on .beta.-phenylthio radicalsJournal of the American Chemical Society, 1976
- Stereoselective Synthesis of Trisubstituted OlefinsSynthesis, 1971
- β-Nitrosulfides and β-AminosulfidesJournal of the American Chemical Society, 1951