dc.contributor.author
Tortajada, Andreu
dc.contributor.author
Ryo, Ninokata
dc.contributor.author
Martín, Rubén
dc.date.accessioned
2018-03-26T14:58:45Z
dc.date.accessioned
2024-04-23T10:18:47Z
dc.date.available
2019-01-27T01:45:06Z
dc.date.available
2024-04-23T10:18:47Z
dc.date.issued
2018-01-27
dc.identifier.uri
http://hdl.handle.net/2072/307101
dc.description.abstract
A site-selective catalytic incorporation of multiple CO2 molecules into 1,3-dienes en route to adipic acids is described. This protocol is characterized by its mild conditions, excellent chemo- and regioselectivity and ease of execution under CO2 (1 atm), including the use of bulk butadiene and/or isoprene feedstocks.
eng
dc.format.extent
5 p.
cat
dc.publisher
American Chemical Society
cat
dc.relation.ispartof
Journal of the American Chemical Society
cat
dc.rights
© American Chemical Society
dc.source
RECERCAT (Dipòsit de la Recerca de Catalunya)
dc.subject.other
54 - Química
cat
dc.title
Ni-Catalyzed Site-Selective Dicarboxylation of 1,3-Dienes with CO2
cat
dc.type
info:eu-repo/semantics/article
cat
dc.type
info:eu-repo/semantics/acceptedVersion
cat
dc.embargo.terms
12 mesos
cat
dc.identifier.doi
https://doi.org/10.1021/jacs.7b13220
dc.rights.accessLevel
info:eu-repo/semantics/openAccess
