Jump to main content
Jump to site search

Issue 13, 2013
Previous Article Next Article

Gold catalyzed stereoselective tandem hydroamination–formal aza-Diels–Alder reaction of propargylic amino esters

Author affiliations

Abstract

A gold-catalyzed tandem intramolecular hydroamination–formal aza-Diels–Alder reaction of propargylic amino esters is described. The overall process leads to the formation of a tetracyclic framework as a single diastereoisomer, with the creation of four bonds and five stereocenters.

Graphical abstract: Gold catalyzed stereoselective tandem hydroamination–formal aza-Diels–Alder reaction of propargylic amino esters

Back to tab navigation

Supplementary files

Publication details

The article was received on 27 Oct 2012, accepted on 21 Dec 2012 and first published on 03 Jan 2013


Article type: Communication
DOI: 10.1039/C2CC37796A
Citation: Chem. Commun., 2013,49, 1336-1338
  •   Request permissions

    Gold catalyzed stereoselective tandem hydroamination–formal aza-Diels–Alder reaction of propargylic amino esters

    S. Fustero, P. Bello, J. Miró, M. Sánchez-Roselló, M. A. Maestro, J. González and C. D. Pozo, Chem. Commun., 2013, 49, 1336
    DOI: 10.1039/C2CC37796A

Search articles by author

Spotlight

Advertisements