Heck-Mizoroki coupling of vinyliodide and applications in the synthesis of dienes and trienes.

Whiting, Andrew
Madden, Katrina S.
David, Sylvain
Knowles, Jonathan P.

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Publication date

July 2015

DOI

10.1039/C5CC03273C

Publisher

Royal Society of Chemistry (RSC)

ISSN

1359-7345

Journal

Chemical Communications

Language

English

Citation count (estimate)

Abstract

Vinyliodide reacts chemoselectively under Heck-Mizoroki conditions with terminal alkenes, including vinylboronate esters, to give dienes. The resulting dienylboronates undergo Suzuki-Miyaura coupling with aryl, heteroaryl and alkenyl halides to access dienes and trienes

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Heck-Mizoroki coupling of vinyliodide and applications in the synthesis of dienes and trienes.

Abstract

Extracted data

Heck-Mizoroki coupling of vinyliodide and applications in the synthesis of dienes and trienes.

Abstract

Extracted data

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