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

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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",

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doi = "10.1039/c8cc02445f",

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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 - https://www.scopus.com/pages/publications/85047771668

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

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