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Redox-Neutral Cyanoalkylation/Cyclization of Olefinic 1,3-Dicarbonyls with Cycloketone Oxime Esters: Access to Cyanoalkylated Dihydrofurans
The Journal of Organic Chemistry ( IF 3.3 ) Pub Date : 2018-03-20 00:00:00 , DOI: 10.1021/acs.joc.8b00271
Jia-Yu Zhang 1 , Xin-Hua Duan 1 , Jun-Cheng Yang 1 , Li-Na Guo 1
Affiliation  

Metal-catalyzed cyanoalkylation/cyclization of olefinic 1,3-dicarbonyls with cycloketone oxime esters has been developed under redox-neutral conditions. This protocol provided a straightforward approach to diverse cyanoalkylated 2,3-dihydrofurans via a tandem ring-opening/addition/cyclization process.

中文翻译:

氧化还原-中性氰基烷基化/烯烃1,3-二羰基与环酮肟酯的环化:氰基烷基化的二氢呋喃的获得

在氧化还原中性条件下,已经开发了用环酮肟酯对烯烃的1,3-二羰基进行金属催化的氰基烷基化/环化反应。该协议提供了一种通过串联开环/加成/环化工艺来处理各种氰基烷基化的2,3-二氢呋喃的直接方法。
更新日期:2018-03-20
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