BF3·OEt2-mediated one pot synthesis of 10-indolyldibenzo[b,f]azepine derivatives via tandem ring expansion and C-C bond formation

Trimurtulu Kotipalli, Donala Janreddy, Veerababurao Kavala, Chun Wei Kuo, Ting Shen Kuo, Mei Ling Chen, Chiu Hui He, Ching Fa Yao

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

A simple and efficient one pot protocol was developed for the synthesis of new structurally diverse 10-indolyldibenzo[b,f]azepine derivatives. The reaction involves Lewis-acid mediated ring expansion followed by C-C bond formation through nucleophilic addition of indole moiety. This journal is

Original languageEnglish
Pages (from-to)47833-47840
Number of pages8
JournalRSC Advances
Volume4
Issue number88
DOIs
Publication statusPublished - 2014

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Azepines
Lewis Acids
Derivatives
Acids
indole

ASJC Scopus subject areas

  • Chemistry(all)
  • Chemical Engineering(all)

Cite this

BF3·OEt2-mediated one pot synthesis of 10-indolyldibenzo[b,f]azepine derivatives via tandem ring expansion and C-C bond formation. / Kotipalli, Trimurtulu; Janreddy, Donala; Kavala, Veerababurao; Kuo, Chun Wei; Kuo, Ting Shen; Chen, Mei Ling; He, Chiu Hui; Yao, Ching Fa.

In: RSC Advances, Vol. 4, No. 88, 2014, p. 47833-47840.

Research output: Contribution to journalArticle

Kotipalli, Trimurtulu ; Janreddy, Donala ; Kavala, Veerababurao ; Kuo, Chun Wei ; Kuo, Ting Shen ; Chen, Mei Ling ; He, Chiu Hui ; Yao, Ching Fa. / BF3·OEt2-mediated one pot synthesis of 10-indolyldibenzo[b,f]azepine derivatives via tandem ring expansion and C-C bond formation. In: RSC Advances. 2014 ; Vol. 4, No. 88. pp. 47833-47840.
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