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An efficient entry to 1,2-benzisoxazoles via1,3-dipolar cycloaddition of in situ generated nitrile oxides and benzyne†
Christopher Mason,Fengzhi Zhang,Dougal J. Ritson,Steve Keeling,John E. Moses
Organic & Biomolecular Chemistry Pub Date : 04/07/2010 00:00:00 , DOI:10.1039/B927235F
Abstract

An efficient protocol for the synthesis of a range of 1,2-benzisoxazoles using an improved 1,3-dipolar cycloaddition of nitrile oxides and benzyne is described. Key to the procedure is the in situ generation of the reactive nitrile oxide and benzyne reactants simultaneously.

Graphical abstract: An efficient entry to 1,2-benzisoxazoles via 1,3-dipolar cycloaddition of in situ generated nitrile oxides and benzyne
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