环丁烷
环己烷类
环加成
化学
分子间力
环己烷
组合化学
基质(水族馆)
立体化学
反应条件
印丹
计算化学
环庚烷
有机化学
有机合成
环己酮
迪亚德
萘
化学合成
立体选择性
作者
Min Zhao,Zhengwei Ding,Saima Perveen,Lulu Qin,Zaicheng Nie,Tao Yu,Mingming Mao,Yuanyuan Cheng,Junyu Wang,Pengfei Li
标识
DOI:10.1021/acs.joc.6c00183
摘要
The cyclohexane skeleton is ubiquitous in small-molecule drugs and bioactive natural products. However, there remains a lack of synthetic methods for polysubstituted cyclohexanes that simultaneously satisfy the requirements of readily available starting materials, high atom economy, and low-cost catalysts, which to a certain extent limits the application of this type of skeleton in the field of drug research and development. Herein, we report the first example of a boron radical-catalyzed intermolecular (4 + 2) cycloaddition reaction between cyclobutanes and alkenes, a strategy that provides an efficient and general method for the synthesis of polysubstituted cyclohexanes. This reaction exhibits broad substrate scope, being compatible with monosubstituted, 1,1-disubstituted, and trisubstituted alkenes and can selectively construct tri-, tetra-, and pentasubstituted cyclohexane derivatives in moderate-to-excellent yields.
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