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Abe Noritaka

Affiliate Master Yamaguchi University

Synthesis of Aryl Conjugated (1-Azaazulenyl)acetylenes and Facile Synthesis of Thiophene Fused 1-Azaazulenes

Heterocycles Volume 72 Page 459-468
published_at 2007
2007020139.pdf
[fulltext] 2.18 MB
Title
Synthesis of Aryl Conjugated (1-Azaazulenyl)acetylenes and Facile Synthesis of Thiophene Fused 1-Azaazulenes
Creators Abe Noritaka
Creators Harada Yohei
Creators Imachi Yukiko
Creators Fujii Hiroyuki
Creators Kakehi Akikazu
Creators Shiro Motoo
3-Ethynyl-1-azaazulene derivatives were obtained by Sonogashira-Hagihara reaction of 3-iodo-2-chloro-1-azaazulenes, and 2-(phenylethynyl)-1-azaazulenes were obtained by the reaction of 2-bromo-1-azaazulenes. Glaser reaction of 2-chloro-3-ethynyl-1-azaazulenes gave 1,4-bis(2-chloro-1-azaazulen-3-yl)-1,3-butadiyne. Treatment of 2-chloro-3-ethynyl-1-azaazulene derivatives with sodium hydrosulfide gave corresponding 1-thia-9-azacyclopent[a]azulene derivatives in good yield.
Languages eng
Resource Type journal article
Publishers 日本複素環化学研究所
Date Issued 2007
File Version Version of Record
Access Rights open access
Relations
[ISSN]0385-5414
[NCID]AA00663739
Schools 大学院医学系研究科(理学) 総合科学実験センター