Your browser doesn't support javascript.
loading
Formylation Reaction of Amines Using N-Formylcarbazole.
Kang, Bubwoong; Shimizu, Yuki; Tamura, Yusaku; Fukuda, Eigo; Hamamoto, Ken-Ichiro; Uchida, Yuichiro; Yasuno, Yoko; Nakayama, Atsushi; Satoh, Tetsuya; Kuse, Masaki; Shinada, Tetsuro.
Afiliação
  • Kang B; Graduate School of Agricultural Science, Kobe University.
  • Shimizu Y; Graduate School of Agricultural Science, Kobe University.
  • Tamura Y; Graduate School of Science, Osaka City University (Currently known as Osaka Metropolitan University).
  • Fukuda E; Graduate School of Science, Osaka City University (Currently known as Osaka Metropolitan University).
  • Hamamoto KI; Graduate School of Science, Osaka City University (Currently known as Osaka Metropolitan University).
  • Uchida Y; Graduate School of Agricultural Science, Kobe University.
  • Yasuno Y; Graduate School of Science, Osaka City University (Currently known as Osaka Metropolitan University).
  • Nakayama A; Graduate School of Science, Osaka City University (Currently known as Osaka Metropolitan University).
  • Satoh T; Graduate School of Science, Osaka City University (Currently known as Osaka Metropolitan University).
  • Kuse M; Graduate School of Agricultural Science, Kobe University.
  • Shinada T; Graduate School of Science, Osaka City University (Currently known as Osaka Metropolitan University).
Chem Pharm Bull (Tokyo) ; 70(7): 492-497, 2022.
Article em En | MEDLINE | ID: mdl-35786568
ABSTRACT
Formamides are useful starting materials for pharmaceutical syntheses. Although various synthetic methods have been documented in this regard, the use of N-formylcarbazole as a formylation reagent for amines has not yet been reported. We report here the first examples of the use of N-formylcarbazole for the formylation of amines. The characteristic reactivity of N-formylcarbazole enables the selective formylation of sterically less hindered aliphatic primary and secondary amines. In contrast, sterically bulkier amines and weakly nucleophilic amines such as anilines are less reactive under the reaction conditions.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carbazóis / Aminas Idioma: En Revista: Chem Pharm Bull (Tokyo) Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Carbazóis / Aminas Idioma: En Revista: Chem Pharm Bull (Tokyo) Ano de publicação: 2022 Tipo de documento: Article