Back to Search Start Over

Nickel(0)-Catalyzed Hydroalkenylation of Imines with Styrene and Its Derivatives.

Authors :
Xiao LJ
Zhao CY
Cheng L
Feng BY
Feng WM
Xie JH
Xu XF
Zhou QL
Source :
Angewandte Chemie (International ed. in English) [Angew Chem Int Ed Engl] 2018 Mar 19; Vol. 57 (13), pp. 3396-3400. Date of Electronic Publication: 2018 Feb 26.
Publication Year :
2018

Abstract

A nickel(0)-catalyzed hydroalkenylation of imines with styrene and its derivatives is described. A wide range of aromatic and aliphatic imines directly coupled with styrene and its derivatives, thus providing various synthetically useful allylic amines with up to 95 % yield. The reaction offers a new atom- and step-economical approach to allylic amines by using alkenes instead of alkenyl-metallic reagents. Experiments and DFT calculations showed that TsNH <subscript>2</subscript> promotes the proton transfer from the coordinated olefin to the imine, accompanied by a new C-C bond formation.<br /> (© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Details

Language :
English
ISSN :
1521-3773
Volume :
57
Issue :
13
Database :
MEDLINE
Journal :
Angewandte Chemie (International ed. in English)
Publication Type :
Academic Journal
Accession number :
29399987
Full Text :
https://doi.org/10.1002/anie.201713333