5257-08-9Relevant articles and documents
A one-pot "back-to-front" approach for the synthesis of benzene ring substituted indoles using allylboronic acids
Karan, Ganesh,Sahu, Samrat,Maji, Modhu Sudan
supporting information, p. 5274 - 5277 (2021/06/06)
Synthesis of only benzene ring functionalized indoles and poly-substituted carbazoles is reported via a one-pot triple cascade benzannulation protocol. Usage of differently substituted and readily accessible allylboronic acids as a 3-carbon annulating partner enables diverse aliphatic and aromatic substitution patterns, which is still a daunting task. This scalable synthetic protocol tolerates broad scope, thus enabling further downstream modifications. As an application, carbazole based natural products glycozoline and glycozolinol were synthesized. This journal is
Transition metals in organic synthesis - Part 83#: Synthesis and pharmacological potential of carbazoles
Choi, Taylor A.,Czerwonka, Regina,Forke, Ronny,Jaeger, Anne,Knoell, Jan,Krahl, Micha P.,Krause, Tilo,Reddy, Kethiri R.,Franzblau, Scott G.,Knoelker, Hans-Joachim
, p. 374 - 385 (2008/12/23)
A series of carbazole derivatives with promising pharmacological properties has been prepared using either an iron-mediated or a palladium-catalyzed synthetic approach. The carbazole alkaloids carbazoquinocin C, carbazomadurin A and B, epocarbazolin A and
A REGIOSPECIFIC SYNTHESIS OF CARBAZOLES VIA CONSECUTIVE PALLADIUM-CATALYZED CROSS-COUPLING AND ARYNE-MEDIATED CYCLIZATION
Iwao, Masatomo,Takehara, Hirokazu,Furukawa, Sunao,Watanabe, Mitsuaki
, p. 1483 - 1488 (2007/10/02)
A regiospecific synthesis of carbazoles has been developed using palladium-catalyzed cross-coupling of N-(tert-butoxycarbonyl)-2-tributylstannylanilines with 2- or 3-bromochlorobenzene followed by aryne-mediated cyclization as the key reactions.The carbazole alkaloids, glycozolinine and glycozolidine, were synthesized using this procedure.