ChemInform Abstract: Synthesis of Enantiomerically Pure Mono-, Di-, and Trisubstituted 2- Sulfinylbuta-1,3-dienes, via β-Hydroxy Selenides.
✍ Scribed by P. GOSSELIN; E. BONFAND; C. MAIGNAN
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 33 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
Synthesis of Enantiomerically Pure Mono-, Di-, and Trisubstituted 2-Sulfinylbuta-1,3-dienes, via β-Hydroxy Selenides.
-While deoxygenation of the epoxide (III) results in the exclusive formation of the sulfide (IV), elimination of the hydroxy selenides ( VI) according to the methods of Krief and Reich gives the desired optically active sulfinylbutadienes (VII), which are potentially useful in terpenoid synthesis. -(GOSSELIN, P.; BONFAND,
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