Reductive coupling of imines with redox-active esters by visible light photoredox organocatalysis

Files
Manuscript_revised_.pdf (363.67 KB)

Embargo End Date
2021-01-22

Type
Article

Authors
Jia, Jiaqi
Lefebvre, Quentin
Rueping, Magnus

KAUST Department
Chemical Science Program
KAUST Catalysis Center (KCC)
Physical Science and Engineering (PSE) Division

Date
2020

Submitted Date
2019-11-29

Abstract
The direct alkylation of imines with redox-active esters by visible light photoorganocatalysis provides a direct way for accessing α-branched secondary amines which are found in numerous bioactive molecules.

Citation
Jia, J., Lefebvre, Q., & Rueping, M. (2020). Reductive coupling of imines with redox-active esters by visible light photoredox organocatalysis. Organic Chemistry Frontiers. doi:10.1039/c9qo01428d

Publisher
Royal Society of Chemistry (RSC)

Journal
Organic Chemistry Frontiers

DOI
10.1039/c9qo01428d

Additional Links
http://xlink.rsc.org/?DOI=C9QO01428D

Permanent link to this record
http://hdl.handle.net/10754/661140
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Articles
Chemical Science Program
KAUST Catalysis Center (KCC)
Physical Science and Engineering (PSE) Division