Issue 1, 2018

Iridium catalyzed fragmentation/cyclization of N-butynyl 4,4-dimethylisoxazolidine-3,5-diones: a unique access to multiply substituted pyrroles

Abstract

A unique protocol for the synthesis of substituted and fused pyrroles has been developed through the iridium catalyzed fragmentation/cyclization of related N-butynyl 4,4-dimethylisoxazolidine-3,5-diones in hot ethanol. Both the substitution pattern and electronic properties can affect the reaction rate and yield.

Graphical abstract: Iridium catalyzed fragmentation/cyclization of N-butynyl 4,4-dimethylisoxazolidine-3,5-diones: a unique access to multiply substituted pyrroles

Supplementary files

Article information

Article type
Research Article
Submitted
07 Aug 2017
Accepted
17 Sep 2017
First published
18 Sep 2017

Org. Chem. Front., 2018,5, 46-50

Iridium catalyzed fragmentation/cyclization of N-butynyl 4,4-dimethylisoxazolidine-3,5-diones: a unique access to multiply substituted pyrroles

M. Shen, X. Ren, Y. Pan and H. Xu, Org. Chem. Front., 2018, 5, 46 DOI: 10.1039/C7QO00698E

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