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

Madden, Katrina S., David, Sylvain, Knowles, Jonathan P. and Whiting, Andrew (2015) Heck–Mizoroki coupling of vinyliodide and applications in the synthesis of dienes and trienes. Chemical Communications, 51 (57). pp. 11409-11412. ISSN 1359-7345

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Official URL: https://doi.org/10.1039/c5cc03273c

Abstract

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

Item Type: Article
Subjects: F100 Chemistry
Department: Faculties > Health and Life Sciences > Applied Sciences
Depositing User: Elena Carlaw
Date Deposited: 15 Mar 2019 15:52
Last Modified: 15 Mar 2019 16:00
URI: http://nrl.northumbria.ac.uk/id/eprint/38427

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