Issue 37, 2013

DABCO-promoted synthesis of pyrazoles from tosylhydrazones and nitroalkenes

Abstract

An efficient synthesis of pyrazoles from tosylhydrazones and nitroalkenes was developed. In comparison with the previously reported 1,3-dipolar cycloaddition reaction of diazo compounds with electron-deficient alkenes or alkynes, this methodology proceeded with a sequential Baylis–Hillman/intramolecular cyclization mechanism and a variety of reversed regioselectivity products were prepared in good yields.

Graphical abstract: DABCO-promoted synthesis of pyrazoles from tosylhydrazones and nitroalkenes

Supplementary files

Article information

Article type
Communication
Submitted
12 Jul 2013
Accepted
30 Jul 2013
First published
01 Aug 2013

Org. Biomol. Chem., 2013,11, 6250-6254

DABCO-promoted synthesis of pyrazoles from tosylhydrazones and nitroalkenes

M. Tang, W. Zhang and Y. Kong, Org. Biomol. Chem., 2013, 11, 6250 DOI: 10.1039/C3OB41435C

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