Recent Progress on[3+2] Ring-Expansion Reaction of Cyclopropane with Unsaturated Compounds

doi:10.6023/cjoc201910019

Abstract

Due to its high ring strain, cyclopropanes can react with a variety of unsaturated compounds to construct five- membered carbo- and hetero-cycles through[3+2] ring-expansion reaction. These five-membered compounds are key skeletons of many drugs, natural products and bioactive molecules, and are also an important class of organic intermediates which have wide applications in medicine, agriculture, chemical engineering, organic synthesis and other related areas. Recently, more and more chemists have constructed a lot of complex five-membered carbo- and hetero-cycles by using cyclopropane as a three-carbon synthon, which has promoted the rapid development of focus area. This review summarizes the most recent [3+2] ring-expansion reaction of cyclopropanes with compounds containing unsaturated bonds such as olefins, aldehydes, ketones and nitriles in the past decade. Moreover, the prospects of future development are also discussed.

Key words: cyclopropane, unsaturated bond, [3+2]ring-expansion reaction, five-membered ring

Cite this article

Liu Wenzhu, Dou Lijuan, Mu Weihua. Recent Progress on[3+2] Ring-Expansion Reaction of Cyclopropane with Unsaturated Compounds[J]. Chinese Journal of Organic Chemistry, 2020, 40(5): 1150-1176.

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