Issue 14, 2014

Polysubstituted pyrrole derivatives via 1,2-alkenyl migration of novel γ-amino-α,β-unsaturated aldehydes and α-diazocarbonyls

Abstract

Tri-substituted pyrrole derivatives were successfully synthesized from aminoaldehyde and α-diazocarbonyl, using a TiCl4 catalyst. The reactions proceeded via 1,2-migration and condensation, leading to the corresponding pyrroles in moderate to excellent yields. Reaction susceptibility was subsequently demonstrated by the variation in substrates.

Graphical abstract: Polysubstituted pyrrole derivatives via 1,2-alkenyl migration of novel γ-amino-α,β-unsaturated aldehydes and α-diazocarbonyls

Supplementary files

Article information

Article type
Communication
Submitted
26 Nov 2013
Accepted
07 Jan 2014
First published
08 Jan 2014

RSC Adv., 2014,4, 7275-7278

Polysubstituted pyrrole derivatives via 1,2-alkenyl migration of novel γ-amino-α,β-unsaturated aldehydes and α-diazocarbonyls

S. Cai, J. Zeng, Y. Li and X. Liu, RSC Adv., 2014, 4, 7275 DOI: 10.1039/C3RA47020B

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