dc.contributor.author
Serrano, Eloisa
dc.contributor.author
Martin, Ruben
dc.date.accessioned
2018-01-15T16:04:07Z
dc.date.accessioned
2018-02-15T10:29:04Z
dc.date.accessioned
2024-04-23T10:36:36Z
dc.date.available
2018-01-15T16:04:07Z
dc.date.available
2018-02-15T10:29:04Z
dc.date.available
2024-04-23T10:36:36Z
dc.identifier.uri
http://hdl.handle.net/2072/305944
dc.description.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>
dc.relation
European Research Council (ERC- 277883)
dc.relation
MINECO (CTQ2015-65496-R
dc.relation
Severo Ochoa Excellence Accreditation 2014-2018
dc.relation
European Research Council (ERC- 277883), MINECO (CTQ2015-65496-R and Severo Ochoa Excellence Accreditation 2014-2018, SEV-2013-0319), FEDER & Cellex
dc.relation.ispartof
Angew. Chem. Int. Ed
dc.rights
© 1999 - 2016 John Wiley & Sons, Inc.
dc.title
Nickel-Catalyzed Reductive Amidation of Unactivated Alkyl Bromides
dc.type
info:eu-repo/semantics/article
dc.relation.projectID
info:eu-repo/grantAgreement/ERC/FP7/277883
dc.relation.projectID
MINECO (CTQ2015-65496-R
dc.relation.projectID
Severo Ochoa Excellence Accredi
dc.identifier.doi
https://doi.org/10.1002/anie.201605162
dc.rights.accessLevel
info:eu-repo/semantics/openAccess
