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ID 57467
Author
Mitsudo, Koichi Division of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University ORCID Kakenhi publons
Yoshioka, Kazuki Division of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University
Hirata, Takayuki Division of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University
Mandai, Hiroki Division of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University ORCID Kakenhi publons
Midorikawa, Koji Division of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University
Suga, Seiji Division of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University ORCID Kakenhi
Abstract
A 1,10-phenanthroline-promoted cyanation of aryl iodides has been developed. 1,10-Phenanthroline worked as an organocatalyst for the reaction of aryl iodides with tetraalkylammonium cyanide to afford aryl cyanides. A similar reaction occurred through an electroreductive process.
Keywords
cyanation
organocatalysis
electrochemistry
aryl iodides
aryl cyanides
Note
This fulltext will be available in Jun 2020
Published Date
2019-06
Publication Title
Synlett
Volume
volume30
Issue
issue10
Publisher
GEORG THIEME
Start Page
1209
End Page
1214
ISSN
09365214
NCID
AA10731110
Content Type
Journal Article
language
英語
OAI-PMH Set
岡山大学
File Version
author
DOI
Web of Sience KeyUT
Related Url
isVersionOf https://doi.org/10.1055/s-0037-1611793
Funder Name
Japan Society for the Promotion of Science
助成番号
16K05695 : 電気化学的に発生させた有機金属種を用いる選択的カップリング反応の開発 Research Project
16K05777 : 環状イミニウムカチオンと炭素求核剤の反応における立体化学の逆転現象
16H01155 : マイクロフローシステムによる高活性反応プロモーターの発生と合成反応の集積化
18H04415 : 反応集積化に適した高活性反応プロモーターを用いるマイクロフローシステムの開発