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Convenient enantioselective synthesis of new 1,4-sulfanylalcohols from γ-lactones

✍ Scribed by Jean-Jacques Filippi; Xavier Fernandez; Louisette Lizzani-Cuvelier; André-Michel Loiseau


Publisher
Elsevier Science
Year
2002
Tongue
French
Weight
119 KB
Volume
43
Category
Article
ISSN
0040-4039

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✦ Synopsis


A synthetic strategy based upon three basic reactions-enzymatic resolution, oxygen-sulfur exchange, reductionallowed us to carry out an easy and useful synthesis of a series of new 1,4-sulfanylalcohols from aliphatic g-lactones. Final products have been obtained in good yields with enantiomeric excesses in a 66-91% range.


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