Synthesis of spiro-4H-pyrazole-oxindoles and fused 1H-pyrazoles via divergent, thermally induced tandem cyclization/migration of alkyne-tethered diazo compounds†
Cheng Zhang,Shanliang Dong,Yang Zheng,Ciwang He,Jiaolong Chen,Jingsen Zhen,Lihua Qiu,Xinfang Xu
Organic & Biomolecular Chemistry Pub Date : 12/06/2017 00:00:00 , DOI:10.1039/C7OB02802D
Abstract

A thermally induced, substrate-dependent reaction of alkynyl diazo compounds has been developed. This transformation produces spiro-4H-pyrazole-oxindoles and fused 1H-pyrazoles in good to high yields from the corresponding alpha-cyano and alpha-sulfonyl diazo compounds. The salient features of this reaction include excellent chemoselectivity and atom-economy, mild reaction conditions, simple purification and potential for large scale production.

Graphical abstract: Synthesis of spiro-4H-pyrazole-oxindoles and fused 1H-pyrazoles via divergent, thermally induced tandem cyclization/migration of alkyne-tethered diazo compounds