Issue 76, 2016

Gold-catalyzed [3+2]-annulations of α-aryl diazonitriles with ynamides and allenamides to yield 1-amino-1H-indenes

Abstract

Gold-catalyzed [3+2]-annulations of α-aryl diazonitriles with ynamides and allenamides yield 1-amino-1H-indenes in two distinct pathways; the success of these annulations relies on the high electrophilicity of α-cyano arylgold carbenes to activate an ionic pathway.

Graphical abstract: Gold-catalyzed [3+2]-annulations of α-aryl diazonitriles with ynamides and allenamides to yield 1-amino-1H-indenes

Supplementary files

Article information

Article type
Communication
Submitted
25 May 2016
Accepted
19 Aug 2016
First published
22 Aug 2016

Chem. Commun., 2016,52, 11434-11437

Gold-catalyzed [3+2]-annulations of α-aryl diazonitriles with ynamides and allenamides to yield 1-amino-1H-indenes

R. R. Singh, S. K. Pawar, M. Huang and R. Liu, Chem. Commun., 2016, 52, 11434 DOI: 10.1039/C6CC04308A

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