Protocols for the Syntheses of 2,2′-Bis(indolyl)arylmethanes, 2-Benzylated lndoles, and 5,7-Dihydroindolo[2,3-<i>b</i>]carbazoles

Lafzi F., KILIÇ H., SARAÇOĞLU N.

JOURNAL OF ORGANIC CHEMISTRY, cilt.84, sa.18, ss.12120-12130, 2019 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 84 Sayı: 18
  • Basım Tarihi: 2019
  • Doi Numarası: 10.1021/acs.joc.9b02124
  • Dergi Adı: JOURNAL OF ORGANIC CHEMISTRY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Index Chemicus (IC), Current Chemical Reactions (CCR)
  • Sayfa Sayıları: ss.12120-12130
  • Ankara Üniversitesi Adresli: Hayır

Özet

The electrophilic substitution reaction of 4,7-dihydroindole with aryl-aldehydes as an electrophilic partner followed by an oxidation step to deliver 2,2'-bis(indolyl)arylmethanes was studied for the first time. The reaction afforded regioselectivity at the 2,2'-positions of indole in an operationally simple and inexpensive procedure with a variety of substrates. To the best of our knowledge, this is the first set of examples of 2,2'-bis(indolyl)arylmethanes obtained in a substituent-free manner. A facile method from dipyrromethanes to the corresponding 2-benzylindoles was also reported. In addition, 2,2'-bis(indolyl)arylmethanes were converted to 5,7-dihydroindolo[2,3-b]carbazoles.