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Diasteroselective and Enantioselective Ir-Catalyzed Allylic Substitutions of 1-Substituted 1-Fluoro-1-(arenesulfonyl)methylene Derivatives
The Journal of Organic Chemistry ( IF 3.6 ) Pub Date : 2017-09-18 00:00:00 , DOI: 10.1021/acs.joc.7b01782
Jiteng Chen 1, 2 , Xiaoming Zhao 1, 2 , Wenyan Dan 1, 2
Affiliation  

diasteroselective and enantioselective Ir-catalyzed allylic substitutions of 1-substituted 1-fluoro-1-(arenesulfonyl)methylene derivatives are presented, which afford the fluorinated allyl products with two chirality centers. The steric demand of 1-substituted 1-fluoro-1-(arenesulfonyl)methylene derivatives and allylic substrates has a great influence on the dr values of these reactions. The transformation of the branched allyl product into the fluorinated 3,4-dihydro-2H-pyrrole 1-oxide was discussed, as well.

中文翻译:

1-取代的1-氟-1-(芳烃磺酰基)亚甲基衍生物的非对映选择性和对映选择性Ir催化的烯丙基取代

提出了1-取代的1-氟-1-(芳烃磺酰基)亚甲基衍生物的非对映选择性和对映选择性Ir催化的烯丙基取代,其提供了具有两个手性中心的氟化烯丙基产物。1-取代的1-氟-1-(芳烃磺酰基)亚甲基衍生物和烯丙基底物的空间需求对这些反应的dr值有很大影响。还讨论了支链烯丙基产物向氟化的3,4-二氢-2 H-吡咯1-氧化物的转化。
更新日期:2017-09-19
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