1173913-69-3Relevant academic research and scientific papers
Synthesis of indolylquinolines, indolylacridines, and indolylcyclopenta[b] quinolines from the Baylis-Hillman adducts: An in situ [1,3]-sigmatropic rearrangement of an indole nucleus to access indolylacridines and indolylcyclopenta[b]quinolines
Ramesh, Chintakunta,Lei, Po-Min,Janreddy, Donala,Kavala, Veerababurao,Kuo, Chun-Wei,Yao, Ching-Fa
, p. 8451 - 8464 (2012/11/07)
A simple and easy route to the synthesis of a variety of structurally diverse indolylquinolines, indolylacridines, and indolylcyclopenta[b]quinoline derivatives via the reductive cyclization of C-alkylated indole derivatives, derived from acyclic as well as cyclic Baylis-Hillman adducts with indoles, is described. An unusual in situ [1,3]-sigmatropic rearrangement of the indole nucleus was observed during the reductive cyclicization of α- regioselective B-H adducts containing indoles to produce indolylacridines and indolylcyclopenta[b]quinoline derivatives.
Novel synthesis of indolylquinoline derivatives via the C-alkylation of Baylis-Hillman adducts
Ramesh, Chintakunta,Kavala, Veerababurao,Raju, B. Rama,Kuo, Chun-Wei,Yao, Ching-Fa
experimental part, p. 4037 - 4041 (2009/10/11)
A new and simple method for the C-alkylation of indoles by various Baylis-Hillman adducts and the one-pot reductive cyclization of C-alkylated indole derivatives generated from 2-nitro-Baylis-Hillman adduct to form indolylquinoline derivatives is describe
