dc.contributor.author
Moragas, Toni
dc.contributor.author
Martin, Ruben
dc.date.accessioned
2018-01-15T16:03:47Z
dc.date.accessioned
2018-02-15T10:28:47Z
dc.date.accessioned
2024-04-23T10:33:52Z
dc.date.available
2018-01-15T16:03:47Z
dc.date.available
2018-02-15T10:28:47Z
dc.date.available
2024-04-23T10:33:52Z
dc.identifier.uri
http://hdl.handle.net/2072/305895
dc.description.abstract
<div> <p> A Ni-catalyzed reductive carboxylation technique en route to cyclopropyl carboxylic acids has been developed. This user-friendly and mild transformation operates at atmospheric pressure of CO <sub>2 </sub>and utilizes either organic halides or alkene precursors, thus representing the first example of catalytic reductive carboxylation of secondary counterparts lacking adjacent p-components.</p> </div> <p> </p>
dc.relation
the European Research Council (ERC-277883)
dc.relation
MINECO (CTQ2012-34054
dc.relation
Severo Ochoa Excellence Accreditation 2014-2018
dc.relation
Cellex Foundat
dc.relation
the European Research Council (ERC-277883), MINECO (CTQ2012-34054 & Severo Ochoa Excellence Accreditation 2014-2018, SEV-2013-0319) and Cellex Foundat
dc.relation.ispartof
Synthesis
dc.rights
© Georg Thieme Verlag Stuttgart · New York
dc.subject.other
Nickel, carboxylation
dc.subject.other
cross-coupling
dc.subject.other
carbon dioxide
dc.subject.other
catalysis
dc.title
Ni-catalyzed Reductive Carboxylation of Cyclopropyl Motifs with CO2
dc.type
info:eu-repo/semantics/article
dc.relation.projectID
info:eu-repo/grantAgreement/ERC/FP7/277883
dc.relation.projectID
MINECO (CTQ2012-34054
dc.relation.projectID
Severo Ochoa Excellence Accreditation 2014-2018, SEV-2013-0319
dc.identifier.doi
https://doi.org/10.1055/s-0035-1560439
dc.rights.accessLevel
info:eu-repo/semantics/openAccess
