ID 61271
フルテキストURL
著者
Chen, Qiang Graduate School of Natural Science and Technology, Okayama University
Fu, Liyan Graduate School of Natural Science and Technology, Okayama University
You, Jingwen Graduate School of Natural Science and Technology, Okayama University
Nishihara, Yasushi Research Institute for Interdisciplinary Science, Okayama University ORCID Kaken ID publons researchmap
抄録
Nickel-catalyzed decarbonylative alkynylation of acyl fluorides with terminal silylethynes under copper-free conditions is described. This newly developed method has a wide substrate scope, affording internal silylethynes in moderate to high yields. The formation of 1,3-diynes as homocoupled products and conjugate enones as carbonyl-retentive products were effectively suppressed.
キーワード
nickel catalysis
decarbonylation
silylalkynes
alkynylation
acyl fluorides
sila-Sonogashira–Hagihara reaction
備考
This is an Accepted Manuscript of an article published by Thieme Gruppe.
発行日
2020-10-28
出版物タイトル
Synlett
出版者
Thieme Gruppe
ISSN
0936-5214
NCID
AA10731110
資料タイプ
学術雑誌論文
言語
英語
OAI-PMH Set
岡山大学
著作権者
© 2020. Thieme.
論文のバージョン
author
DOI
Web of Science KeyUT
関連URL
isVersionOf https://doi.org/10.1055/s-0040-1705954
過去1年のアクセス数
アクセス数 : ?
ダウンロード数 : ?

今月のアクセス数
アクセス数 : ?
ダウンロード数 : ?