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HERO ID
4271818
Reference Type
Journal Article
Title
Palladium-catalyzed regioselective hydroboration of aryl alkenes with B2pin2
Author(s)
Huang, J; Yan, W; Tan, C; Wu, W; Jiang, H
Year
2018
Is Peer Reviewed?
Yes
Journal
Chemical Communications
ISSN:
1359-7345
EISSN:
1364-548X
Volume
54
Issue
14
Page Numbers
1770-1773
Language
English
PMID
29383345
DOI
10.1039/c7cc09432a
Web of Science Id
WOS:000425105800023
URL
https://www.proquest.com/docview/2221009718?accountid=171501&bdid=64576&_bd=HmLSN3D0Ee8AMlD5y9%2BFP9%2BXEGM%3D
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Abstract
A palladium(ii)-catalyzed hydroboration of aryl alkenes with stable and easy-to-handle (pinacolato)diboron (B2pin2) under mild conditions has been developed. Acetic acid acted as the solvent and the hydrogen source, which has been identified by deuterium experiments. Notably, isomerization-hydroboration of allyl benzene derivatives was observed. As a result, a series of benzyl boronic esters were obtained in moderate to excellent yields with exclusive regioselectivity.
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