Issue 32, 2015

De novo synthesis of functionalized 1,3-enynes and extended conjugated molecular systems

Abstract

Pd-catalyzed coupling of 1,3-dienyldibromides with triarylbismuths was demonstrated for the synthesis of a diverse range of 1,3-enynes. This study provided easy access to a range of functionalized 1,3-enynes in high yields utilizing triarylbismuths in sub-stoichiometric amounts. A new and concise route was unveiled for the synthesis of extended π-conjugated molecular systems with the help of chemoselective couplings and in conjunction with Sonogashira, Heck and arylation reactions under combined catalysis.

Graphical abstract: De novo synthesis of functionalized 1,3-enynes and extended conjugated molecular systems

Supplementary files

Article information

Article type
Paper
Submitted
26 Jan 2015
Accepted
26 Feb 2015
First published
09 Mar 2015

RSC Adv., 2015,5, 24834-24845

De novo synthesis of functionalized 1,3-enynes and extended conjugated molecular systems

M. L. N. Rao, P. Dasgupta and V. N. Murty, RSC Adv., 2015, 5, 24834 DOI: 10.1039/C5RA01544H

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