Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/79348
Title: Cobalt-catalyzed intermolecular hydroacylation of olefins through chelation-assisted imidoyl C-H activation
Authors: Yang, Junfeng
Seto, Yuan Wah
Yoshikai, Naohiko
Keywords: DRNTU::Science::Chemistry::Organic chemistry
Issue Date: 2015
Source: Yang, J., Seto, Y. W., & Yoshikai, N. (2015). Cobalt-catalyzed intermolecular hydroacylation of olefins through chelation-assisted imidoyl C-H activation. ACS Catalysis, 5(5), 3054-3057.
Series/Report no.: ACS catalysis
Abstract: A low-valent cobalt catalyst generated from cobalt(II) bromide, a diphosphine ligand, and zinc powder promotes intermolecular hydroacylation of olefins using N-3-picolin-2-yl aldimines as aldehyde equivalents, which affords, upon acidic hydrolysis, ketone products in moderate to good yields with high linear selectivity. The reaction is applicable to styrenes, vinylsilanes, and aliphatic olefins as well as to various aryl and heteroaryl aldimines. The cobalt catalysis features a distinctively lower reaction temperature (60 °C) compared with those required for the same type of transformations catalyzed by rhodium complexes (typically 130–150 °C).
URI: https://hdl.handle.net/10356/79348
http://hdl.handle.net/10220/38495
DOI: 10.1021/acscatal.5b00581
Schools: School of Physical and Mathematical Sciences 
Rights: © 2015 American Chemical Society. This is the author created version of a work that has been peer reviewed and accepted for publication by ACS Catalysis, American Chemical Society. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1021/acscatal.5b00581].
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SPMS Journal Articles

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