Electron transfer-induced reduction of organic halides with amines

Takahide Fukuyama; Yuki Fujita; Hayato Miyoshi; Ilhyong Ryu; Shih Chieh Kao; Yen-Ku Wu

doi:10.1039/c8cc02445f

Electron transfer-induced reduction of organic halides with amines

Takahide Fukuyama, Yuki Fujita, Hayato Miyoshi, Ilhyong Ryu^*, Shih Chieh Kao, Yen-Ku Wu

^*Corresponding author for this work

Department of Applied Chemistry

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

43 Scopus citations

Abstract

Reduction of a variety of organo halides was examined by using amines as a sacrificial hydrogen source. UV light-induced reduction of vinyl and aryl halides with triethylamine proceeded smoothly to give the corresponding reduced products. High temperature heating also caused the reduction and DABCO (1,4-diazabicyclo[2.2.2]octane) also served as a good reducing reagent.

Original language	English
Pages (from-to)	5582-5585
Number of pages	4
Journal	Chemical Communications
Volume	54
Issue number	44
DOIs	https://doi.org/10.1039/c8cc02445f
State	Published - 3 May 2018

Access to Document

10.1039/c8cc02445f

Cite this

@article{f755b03b3e024a97ac19260ed9799c82,

title = "Electron transfer-induced reduction of organic halides with amines",

abstract = "Reduction of a variety of organo halides was examined by using amines as a sacrificial hydrogen source. UV light-induced reduction of vinyl and aryl halides with triethylamine proceeded smoothly to give the corresponding reduced products. High temperature heating also caused the reduction and DABCO (1,4-diazabicyclo[2.2.2]octane) also served as a good reducing reagent.",

author = "Takahide Fukuyama and Yuki Fujita and Hayato Miyoshi and Ilhyong Ryu and Kao, {Shih Chieh} and Yen-Ku Wu",

note = "Publisher Copyright: {\textcopyright} 2018 The Royal Society of Chemistry.",

year = "2018",

month = may,

day = "3",

doi = "10.1039/c8cc02445f",

language = "English",

volume = "54",

pages = "5582--5585",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "44",

}

TY - JOUR

T1 - Electron transfer-induced reduction of organic halides with amines

AU - Fukuyama, Takahide

AU - Fujita, Yuki

AU - Miyoshi, Hayato

AU - Ryu, Ilhyong

AU - Kao, Shih Chieh

AU - Wu, Yen-Ku

PY - 2018/5/3

Y1 - 2018/5/3

N2 - Reduction of a variety of organo halides was examined by using amines as a sacrificial hydrogen source. UV light-induced reduction of vinyl and aryl halides with triethylamine proceeded smoothly to give the corresponding reduced products. High temperature heating also caused the reduction and DABCO (1,4-diazabicyclo[2.2.2]octane) also served as a good reducing reagent.

AB - Reduction of a variety of organo halides was examined by using amines as a sacrificial hydrogen source. UV light-induced reduction of vinyl and aryl halides with triethylamine proceeded smoothly to give the corresponding reduced products. High temperature heating also caused the reduction and DABCO (1,4-diazabicyclo[2.2.2]octane) also served as a good reducing reagent.

UR - http://www.scopus.com/inward/record.url?scp=85047771668&partnerID=8YFLogxK

U2 - 10.1039/c8cc02445f

DO - 10.1039/c8cc02445f

M3 - Article

C2 - 29766164

AN - SCOPUS:85047771668

SN - 1359-7345

VL - 54

SP - 5582

EP - 5585

JO - Chemical Communications

JF - Chemical Communications

IS - 44

ER -

Electron transfer-induced reduction of organic halides with amines

Abstract

Access to Document

Other files and links

Fingerprint

Cite this