Chinese Journal of Organic Chemistry >
Research Progress in the Cyclization Reactions with Propargyl Alcohols
Received date: 2022-03-20
Revised date: 2022-06-12
Online published: 2022-06-23
Supported by
National Natural Science Foundation of China(21961034); National Natural Science Foundation of China(21502154); National Natural Science Foundation of China(21362033); Gansu Provincial Science and Technology Program(21JR1RA232); Industrial Support Program of Gansu Province for Colleges(2021CYZC-17)
Propargyl alcohols as a classical bifunctional group compounds possess alcohol hydroxyl group and carbon-carbon triple bond. Due to their special structure, they show unique reaction characteristics, and are employed in reactions via activating its alcoholic hydroxyl group or triple bond. The most typical reaction for propargyl alcohols is various cyclization reactions with different compounds to assemble a richer variety of cyclized compounds such as cyclopentene, pyrrole, furan, cyclic carbonate, pyran, pyridine and azepine cyclic compounds. The recent research progress in the cyclization reaction of propargyl alcohols with various compounds, including [3+2], [2+3], [3+3], [4+2], [2+4], [4+1], [3+4] and other types of cyclization reactions, is summarized.
Xiaozheng Zhao , Qinqin Ling , Guiyan Cao , Xing Huo , Xiaolong Zhao , Yingpeng Su . Research Progress in the Cyclization Reactions with Propargyl Alcohols[J]. Chinese Journal of Organic Chemistry, 2022 , 42(9) : 2605 -2639 . DOI: 10.6023/cjoc202203037
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