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Issue 35, 2015
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Peroxide promoted tunable decarboxylative alkylation of cinnamic acids to form alkenes or ketones under metal-free conditions

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Abstract

A tunable decarboxylative alkylation of cinnamic acids with alkanes was developed to form alkenes or ketones under transition metal-free conditions. In the presence of DTBP or DTBP/TBHP, the reaction gave alkenes and ketones respectively via a radical mechanism in moderate to good yields.

Graphical abstract: Peroxide promoted tunable decarboxylative alkylation of cinnamic acids to form alkenes or ketones under metal-free conditions

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Supplementary files

Article information


Submitted
01 Mar 2015
Accepted
22 Mar 2015
First published
24 Mar 2015

Chem. Commun., 2015,51, 7546-7549
Article type
Communication
Author version available

Peroxide promoted tunable decarboxylative alkylation of cinnamic acids to form alkenes or ketones under metal-free conditions

J. Ji, P. Liu and P. Sun, Chem. Commun., 2015, 51, 7546 DOI: 10.1039/C5CC01762A

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