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区域和对映选择性钯催化的硝基甲烷与单取代烯丙基底物的烯丙基烷基化反应:(R)-罗利普兰和(R)-巴氯芬的合成。

Regio- and enantioselective palladium-catalyzed allylic alkylation of nitromethane with monosubstituted allyl substrates: synthesis of (R)-rolipram and (R)-baclofen.

机构信息

State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, People's Republic of China.

出版信息

J Org Chem. 2012 Oct 19;77(20):8980-5. doi: 10.1021/jo301506p. Epub 2012 Oct 1.

Abstract

The Pd-catalyzed asymmetric allylic alkylation (AAA) reaction of nitromethane with monosubstituted allyl substrates was realized for the first time to provide corresponding products in high yields with excellent regio- and enantioselectivities. The protocol was applied to the enantioselective synthesis of (R)-baclofen and (R)-rolipram.

摘要

钯催化的硝基甲烷与单取代烯丙基底物的不对称烯丙基烷基化(AAA)反应首次实现,以高收率和优异的区域和对映选择性提供相应产物。该方案被应用于(R)-巴氯芬和(R)-罗利普兰的对映选择性合成。

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