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

Journal of Organic Chemistry

Volumn 77, Issue 19, 2012, Pages 8451-8464

  Ramesh, Chintakunta ^a   Lei, Po Min ^a   Janreddy, Donala ^a   Kavala, Veerababurao ^a   Kuo, Chun Wei ^a   Yao, Ching Fa ^a  

^a NATIONAL TAIWAN NORMAL UNIVERSITY   (Taiwan)

Author keywords

[No Author keywords available]

Indexed keywords

BAYLIS-HILLMAN ADDUCTS; IN-SITU; INDOLE DERIVATIVES; QUINOLINE DERIVATIVE; REDUCTIVE CYCLIZATION; REGIO-SELECTIVE; SIGMATROPIC REARRANGEMENTS;

CHEMISTRY;

ORGANIC COMPOUNDS;

ACRIDINE DERIVATIVE; INDOLE DERIVATIVE; INDOLYLACRIDINE; INDOLYLCYCLOPENTA[B]QUINOLINE; INDOLYLQUINOLINE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

ALKYLATION; ARTICLE; BAYLIS HILLMAN REACTION; CYCLIZATION; DRUG SYNTHESIS; REACTION ANALYSIS; REDUCTION;

ACRIDINES; ALKYLATION; CYCLIZATION; INDOLES; MOLECULAR STRUCTURE; QUINOLINES;

EID: 84867379825     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo301313m     Document Type: Article

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