Issue 8, 2022

Base-mediated unprecedented tandem cyclization reaction of nitrilimines and sulfur ylides: facile approaches to multifunctionalized pyrazolines

Abstract

An interesting three-component tandem reaction between hydrazonoyl chlorides and α-keto-derived sulfonium salts is reported. Highly substituted pyrazolines were obtained in moderate to excellent yields under mild conditions. Moreover, α-keto-stabilised sulfur ylides served as two-carbon synthons in this tandem [3 + 2] cycloaddition reaction.

Graphical abstract: Base-mediated unprecedented tandem cyclization reaction of nitrilimines and sulfur ylides: facile approaches to multifunctionalized pyrazolines

Supplementary files

Article information

Article type
Research Article
Submitted
11 Feb 2022
Accepted
05 Mar 2022
First published
09 Mar 2022

Org. Chem. Front., 2022,9, 2204-2208

Base-mediated unprecedented tandem cyclization reaction of nitrilimines and sulfur ylides: facile approaches to multifunctionalized pyrazolines

C. Wang, L. Fang, L. Zhang, Y. Wang, F. Gao and Z. Wang, Org. Chem. Front., 2022, 9, 2204 DOI: 10.1039/D2QO00232A

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