P III -Mediated intramolecular cyclopropanation and metal-free synthesis of cyclopropane-fused heterocycles
Jiayong Zhang, Jiahang Hao, Zhiqiang Huang, Jie Han, Zhengjie He
Abstract
Jiayong Zhang, Jiahang Hao, Zhiqiang Huang, Jie Han, Zhengjie He
Abstract
A P(NMe2)3-mediated reductive intramolecular cyclopropanation is developed for the first time, which provides facile access to a wide variety of cyclopropane-fused heterocycles including chromanes, tetrahydroquinolines, lactones, and lactams. Catalytic hydrogenative ring-expansion of the cyclopropane-fused heterocycles is also elaborated, leading to various structurally important medium-sized heterocycles.
OpenAlex reports 35 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
A P(NMe2)3-mediated reductive intramolecular cyclopropanation is developed for the first time, which provides facile access to a wide variety of cyclopropane-fused heterocycles including chromanes, tetrahydroquinolines, lactones, and lactams. Catalytic hydrogenative ring-expansion of the cyclopropane-fused heterocycles is also elaborated, leading to various structurally important medium-sized heterocycles.
Key concepts: Cyclopropanation, Cyclopropane, Intramolecular force, Chemistry, Metal, Stereochemistry, Organic chemistry, Catalysis