Olefin cross-metathesis/Suzuki-Miyaura reactions on 4-vinylphenylboronic acid pinacol ester
Baltus, Christine, Press, Neil, Coles, Simon, Tizzard, Graham, Spencer, John, Chuckowree, Irina and Day, Iain (2013) Olefin cross-metathesis/Suzuki-Miyaura reactions on 4-vinylphenylboronic acid pinacol ester. Tetrahedron Letters, 54 (10). pp. 1211-1217. ISSN 0040-4039
Abstract
A series of alkenyl phenylboronic acid pinacol esters have been synthesized via an olefin cross-metathesis reaction of 4-vinylphenylboronic acid pinacol ester. After catalytic hydrogenation, the resulting boronates were reacted in a microwave-mediated Suzuki-Miyaura coupling reaction to form a library of biarylethyl aryl and cycloalkyl derivatives. A complementary reaction sequence involved an initial Suzuki-Miyaura coupling of 4-vinylphenylboronic acid with aryl halides prior to the cross metathesis reaction and hydrogenation sequence.
Item Type: | Article |
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Additional Information: | Paper resulting from CASE collaboration. No proprietary structures. |
Keywords: | Arylboronic esters, Cross-metathesis reaction, Suzuki-Miyaura coupling, C-C bond formation, Microwaves. |
Date Deposited: | 13 Oct 2015 13:14 |
Last Modified: | 13 Oct 2015 13:14 |
URI: | https://oak.novartis.com/id/eprint/6294 |