Jump to main content
Jump to site search

Issue 28, 2014
Previous Article Next Article

A survey of enoldiazo nucleophilicity in selective C–C bond forming reactions for the synthesis of natural product-like frameworks

Author affiliations

Abstract

A survey of in situ, catalytically generated carbocations for coupling with enoldiazoacetate nucleophiles was performed. These couplings facilitate the rapid assembly of complex organodiazo compounds that provide a template for the synthesis of a variety of carbocyclic and heterocyclic ring systems.

Graphical abstract: A survey of enoldiazo nucleophilicity in selective C–C bond forming reactions for the synthesis of natural product-like frameworks

Back to tab navigation
Please wait while Download options loads

Supplementary files

Publication details

The article was received on 03 Apr 2014, accepted on 30 May 2014 and first published on 03 Jun 2014


Article type: Paper
DOI: 10.1039/C4OB00709C
Citation: Org. Biomol. Chem., 2014,12, 5227-5234
  •   Request permissions

    A survey of enoldiazo nucleophilicity in selective C–C bond forming reactions for the synthesis of natural product-like frameworks

    Y. Liu, Y. Liu, C. S. Shanahan, X. Xu and M. P. Doyle, Org. Biomol. Chem., 2014, 12, 5227
    DOI: 10.1039/C4OB00709C

Search articles by author