dc.contributor.author
Mavroskoufis, Andreas
dc.contributor.author
Jakob, Michael
dc.contributor.author
Hopkinson, Matthew N.
dc.date.accessioned
2020-10-13T13:10:07Z
dc.date.available
2020-10-13T13:10:07Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/28507
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-28256
dc.description.abstract
The combination of N‐heterocyclic carbene (NHC)‐organocatalysis with photochemical activation can lead to unprecedented reaction pathways not observed without light. A selection of dual catalytic systems merging NHCs with photoredox catalysis, for example, have leveraged the ability of NHCs to stabilize intermediate radical species and facilitate single electron transfer events. Furthermore, NHCs can transiently modulate the photochemical properties of a substrate and enable direct absorption of otherwise photoinactive organic compounds. In this Concept article, the recent advances in this rapidly developing field are summarized. For each transformation, a particular focus is placed on the mechanistic aspects of the process while key features that highlight the synthetic potential of the light mediated NHC organocatalysis are presented.
en
dc.rights.uri
https://creativecommons.org/licenses/by-nc/4.0/
dc.subject
N-Heterocyclic carbenes
en
dc.subject
organocatalysis
en
dc.subject
photochemistry
en
dc.subject
photoredox catalysis
en
dc.subject
single electron transfer
en
dc.subject.ddc
500 Naturwissenschaften und Mathematik::540 Chemie::540 Chemie und zugeordnete Wissenschaften
dc.title
Light‐Promoted Organocatalysis with N‐Heterocyclic Carbenes
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.1002/cptc.202000120
dcterms.bibliographicCitation.journaltitle
ChemPhotoChem
dcterms.bibliographicCitation.number
10
dcterms.bibliographicCitation.pagestart
5147
dcterms.bibliographicCitation.pageend
5153
dcterms.bibliographicCitation.volume
4
dcterms.bibliographicCitation.url
https://doi.org/10.1002/cptc.202000120
refubium.affiliation
Biologie, Chemie, Pharmazie
refubium.funding
DEAL Wiley
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.eissn
2367-0932
dcterms.isPartOf.zdb
2881321-2