Nickel-Catalyzed Reductive Amidation of Unactivated Alkyl Bromides

Author

Serrano, Eloisa

Martin, Ruben

Publication date

2016



Abstract

<p> A user-friendly, nickel-catalyzed reductive amidation of unactivated primary, secondary, and tertiary alkyl bromides with isocyanates is described. This catalytic strategy offers an efficient synthesis of a wide range of aliphatic amides under mild conditions and with an excellent chemoselectivity profile while avoiding the use of stoichiometric and sensitive organometallic reagents.</p>

Document Type

Article

Language

English

Publisher

Wiley

Version of

Angew. Chem. Int. Ed

Grant Agreement Number

info:eu-repo/grantAgreement/ERC/FP7/277883

MINECO (CTQ2015-65496-R

Severo Ochoa Excellence Accredi

Related items

European Research Council (ERC- 277883)

MINECO (CTQ2015-65496-R

Severo Ochoa Excellence Accreditation 2014-2018

FEDER

Cellex

European Research Council (ERC- 277883), MINECO (CTQ2015-65496-R and Severo Ochoa Excellence Accreditation 2014-2018, SEV-2013-0319), FEDER & Cellex

Documents

Ni-cat reductive amidation alkylBr-changes.pdf

1.437Mb

 

Rights

© 1999 - 2016 John Wiley & Sons, Inc.

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Papers [1244]