Copper-free cycloaddition of azide and alkyne in crystalline state facilitated by arene-perfluoroarene interactions

Ni, Ben-Bo
Wang, Chong
Wu, Huixian
Pei, Jian
Ma, Yuguo

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Publication date

January 2010

DOI

10.1039/b912337g

Publisher

chemical communications

ISSN

1359-7345

Journal

1359-7345

Abstract

Facilitated by arene-perfluoroarene interactions, a 1,3-dipolar cycloaddition between azide and alkyne proceeded in the crystals at room temperature in the absence of a copper(I) catalyst, and the reaction was confirmed to be a highly regioselective process giving the 1,4-triazole product.http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000274207000035&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=8e1609b174ce4e31116a60747a720701Chemistry, MultidisciplinarySCI(E)PubMed17ARTICLE5782-7844

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Copper-free cycloaddition of azide and alkyne in crystalline state facilitated by arene-perfluoroarene interactions

Abstract

Extracted data

Copper-free cycloaddition of azide and alkyne in crystalline state facilitated by arene-perfluoroarene interactions

Abstract

Extracted data

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