Issue 24, 2016

Expedient synthesis of densely substituted pyrrolo[1,2-a]indoles

Abstract

Cu(OTf)2 catalyzed [6 + 2] cycloaddition reaction of indolyl-2-carbinols with various dienophiles such as indole derived α,β-unsaturated esters, ketones, nitriles and cinnamates is described. The strategy was further applied for the synthesis of optically active pyrrolo[1,2-a]indoles in >97% de using the chiral auxiliary based approach.

Graphical abstract: Expedient synthesis of densely substituted pyrrolo[1,2-a]indoles

  • This article is part of the themed collection: New Talent

Supplementary files

Article information

Article type
Paper
Submitted
21 Apr 2016
Accepted
12 May 2016
First published
12 May 2016

Org. Biomol. Chem., 2016,14, 5843-5860

Expedient synthesis of densely substituted pyrrolo[1,2-a]indoles

D. H. Dethe and R. Boda, Org. Biomol. Chem., 2016, 14, 5843 DOI: 10.1039/C6OB00861E

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