An efficient preparation of optically active (E)-γ-hydroxy-α,β-unsaturated phenyl sulfones using lipase-mediated acylations
✍ Scribed by Esteban Domínguez; Juan Carlos Carretero; Alfonso Fernández-Mayoralas; Santiago Conde
- Publisher
- Elsevier Science
- Year
- 1991
- Tongue
- French
- Weight
- 221 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
A perfect optical resolution of 7 -hydroxystannanes was demonstrated by the method of lipase-catalyzed enantioselective hydrolysis of the corresponding racemic acetates using lipase P(Pw sp.). The utilization of organotin compounds in modern synthesis continues to grow at an impressive rate.') Alth
o!,P-Epoxy esters were rapidly reduced at room temperature to yield P-hydroxy esters with retention of the configurations at the P-carbon atoms by using Sm12-THF-HMPA system in the presence of N,N-dimethylaminoethanol (DMAE). to the synthesis of vinylogous &'-hydroxy esters. The conditions were succ
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