Iridium-Catalyzed Highly Efficient and Site-Selective Deoxygenation of Alcohols

An iridium-catalyzed, highly efficient, and site-selective deoxygenation of primary, secondary, and tertiary alcohols has been realized, under the assistance of a 4-(N-substituted amino)­aryl directing group. Only the hydroxyl adjacent to the directing group can be deoxygenated. The deoxygenation is...

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Bibliographic Details
Published in:ACS catalysis 2018-10, Vol.8 (10), p.9320-9326
Main Authors: Yang, Shiyi, Tang, Weiping, Yang, Zhanhui, Xu, Jiaxi
Format: Article
Language:English
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Summary:An iridium-catalyzed, highly efficient, and site-selective deoxygenation of primary, secondary, and tertiary alcohols has been realized, under the assistance of a 4-(N-substituted amino)­aryl directing group. Only the hydroxyl adjacent to the directing group can be deoxygenated. The deoxygenation is performed in water, with formic acid as both the promoter and hydride donor. Excellent yields and functionality tolerance, as well as high efficiency (S/C up to 1 000 000, TOF up to 445 000 h–1), are obtained. The kinetic isotope effect studies show that hydride formation is the rate-determining step, and the deoxygenation follows an S N 1-type pathway. The deoxygenation protocol has been demonstrated useful in the structural modification of naturally occurring ketones and steroids.
ISSN:2155-5435
2155-5435
DOI:10.1021/acscatal.8b02495