Organocatalytic diimide reduction of enamides in water

Barrie J Marsh; E L Heath; David R Carbery

doi:10.1039/c0cc02272a

Organocatalytic diimide reduction of enamides in water

Barrie J Marsh, E L Heath, David R Carbery

Department of Chemistry

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

42 Citations (SciVal)

Abstract

Bridged flavinium organocatalysts have displayed efficacy in the diimide mediated reduction of enamides in aqueous conditions. This represents the first diimide reduction of an electron rich alkene and offers a clean alternative to the use of alkylating agents for N-alkylation.

Original language	English
Pages (from-to)	280-282
Number of pages	3
Journal	Chemical Communications
Volume	47
Issue number	1
DOIs	https://doi.org/10.1039/c0cc02272a
Publication status	Published - 2010

Access to Document

10.1039/c0cc02272a

Cite this

@article{5328657a34a443b6bbb18b5e88bee43a,

title = "Organocatalytic diimide reduction of enamides in water",

abstract = "Bridged flavinium organocatalysts have displayed efficacy in the diimide mediated reduction of enamides in aqueous conditions. This represents the first diimide reduction of an electron rich alkene and offers a clean alternative to the use of alkylating agents for N-alkylation.",

author = "Marsh, {Barrie J} and Heath, {E L} and Carbery, {David R}",

year = "2010",

doi = "10.1039/c0cc02272a",

language = "English",

volume = "47",

pages = "280--282",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "1",

}

TY - JOUR

T1 - Organocatalytic diimide reduction of enamides in water

AU - Marsh, Barrie J

AU - Heath, E L

AU - Carbery, David R

PY - 2010

Y1 - 2010

N2 - Bridged flavinium organocatalysts have displayed efficacy in the diimide mediated reduction of enamides in aqueous conditions. This represents the first diimide reduction of an electron rich alkene and offers a clean alternative to the use of alkylating agents for N-alkylation.

AB - Bridged flavinium organocatalysts have displayed efficacy in the diimide mediated reduction of enamides in aqueous conditions. This represents the first diimide reduction of an electron rich alkene and offers a clean alternative to the use of alkylating agents for N-alkylation.

UR - http://www.scopus.com/inward/record.url?scp=78649881957&partnerID=8YFLogxK

UR - http://dx.doi.org/10.1039/c0cc02272a

U2 - 10.1039/c0cc02272a

DO - 10.1039/c0cc02272a

M3 - Article

SN - 1359-7345

VL - 47

SP - 280

EP - 282

JO - Chemical Communications

JF - Chemical Communications

IS - 1

ER -

Organocatalytic diimide reduction of enamides in water

Abstract

Access to Document

Other files and links

Fingerprint

Cite this