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Diastereoselective Electrophilic Trifluoromethylthiolation of Chiral Oxazolidinones: Access to Enantiopure α‐SCF3 Alcohols
Advanced Synthesis & Catalysis ( IF 5.4 ) Pub Date : 2018-01-15 , DOI: 10.1002/adsc.201701474
Hélène Chachignon 1 , Evgeniy V. Kondrashov 1, 2 , Dominique Cahard 1
Affiliation  

Lithium imide enolates featuring Evans’ chiral oxazolidinone auxiliary were involved in diastereoselective α‐trifluoromethylthiolation with electrophilic SCF3 donors. Diastereopure products were isolated and converted to enantiopure α‐SCF3 alcohols without racemisation.

中文翻译:

手性恶唑烷酮的非对映选择性亲电子三氟甲基硫醇化:获得对映纯α-SCF3醇

具有Evans手性恶唑烷酮助剂的酰亚胺化锂烯醇盐与亲电子SCF 3供体一起参与非对映选择性α-三氟甲基硫醇化反应。Diastereopure产物分离并转化为对映体纯α-SCF 3个醇无外消旋作用。
更新日期:2018-01-15
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