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

Jiaqi Jia; Quentin Lefebvre; Magnus Rueping

doi:10.1039/c9qo01428d

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

Jiaqi Jia, Quentin Lefebvre, Magnus Rueping

Research output: Contribution to journal › Article › peer-review

34 Scopus citations

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.

Original language	English (US)
Pages (from-to)	602-608
Number of pages	7
Journal	Organic Chemistry Frontiers
Volume	7
Issue number	3
DOIs	https://doi.org/10.1039/c9qo01428d
State	Published - 2020

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https://repository.kaust.edu.sa/bitstream/10754/661140/1/Manuscript_revised_.pdf

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title = "Reductive coupling of imines with redox-active esters by visible light photoredox organocatalysis",

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.",

author = "Jiaqi Jia and Quentin Lefebvre and Magnus Rueping",

note = "KAUST Repository Item: Exported on 2020-10-01",

year = "2020",

doi = "10.1039/c9qo01428d",

language = "English (US)",

volume = "7",

pages = "602--608",

journal = "Organic Chemistry Frontiers",

issn = "2052-4129",

publisher = "Royal Society of Chemistry",

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T1 - Reductive coupling of imines with redox-active esters by visible light photoredox organocatalysis

AU - Jia, Jiaqi

AU - Lefebvre, Quentin

AU - Rueping, Magnus

N1 - KAUST Repository Item: Exported on 2020-10-01

PY - 2020

Y1 - 2020

N2 - 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.

AB - 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.

UR - http://hdl.handle.net/10754/661140

UR - http://xlink.rsc.org/?DOI=C9QO01428D

UR - http://www.scopus.com/inward/record.url?scp=85079294617&partnerID=8YFLogxK

U2 - 10.1039/c9qo01428d

DO - 10.1039/c9qo01428d

M3 - Article

SN - 2052-4129

VL - 7

SP - 602

EP - 608

JO - Organic Chemistry Frontiers

JF - Organic Chemistry Frontiers

IS - 3

ER -

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

Abstract

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