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Building a Cocrystal by Using Supramolecular Synthons for Pressure-Accelerated Heteromolecular Azide-Alkyne Cycloaddition.

作者信息

Meng Xiao, Chen Changqing, Deng Xinyuan, Wang Zhangyuan, Chen Qi, Ma Yuguo

机构信息

Beijing National Laboratory for Molecular Sciences (BNLMS), Center for Soft Matter Science and Engineering, Key Lab of Polymer Chemistry and Physics of Ministry of Education, College of Chemistry, Peking University, Beijing, 100871, P. R. China.

Department of Chemistry and Physics, Salem State University, 352 Lafayette Street, Salem, MA, 01970, USA.

出版信息

Chemistry. 2019 May 23;25(29):7142-7148. doi: 10.1002/chem.201900391. Epub 2019 Apr 11.

DOI:10.1002/chem.201900391
PMID:30873647
Abstract

Facilitated by the supramolecular synthons of carboxylic acids and amides through cooperative hydrogen-bonding and arene-perfluoroarene interactions, the azide-alkyne cycloaddition reaction between two different molecules in a cocrystal was achieved. This reaction could be accelerated by pressure using a common hydraulic press equipment with excellent regioselectivity to yield 1,4-triazole products. The absence of decarboxylation side reactions in the products in the solid state demonstrated that this strategy can provide a green synthetic route for products not directly accessible by traditional syntheses in solution.

摘要

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