Novel synthesis of indolylquinoline derivatives via the C-alkylation of Baylis-Hillman adducts

Chintakunta Ramesh; Veerababurao Kavala; B. Rama Raju; Chun Wei Kuo; Ching Fa Yao

doi:10.1016/j.tetlet.2009.04.064

Novel synthesis of indolylquinoline derivatives via the C-alkylation of Baylis-Hillman adducts

Chintakunta Ramesh
, Veerababurao Kavala
, B. Rama Raju
, Chun Wei Kuo
, Ching Fa Yao^*

^*Corresponding author for this work

Department of Chemistry

Research output: Contribution to journal › Article › peer-review

28 Citations (Scopus)

Abstract

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 described.

Original language	English
Pages (from-to)	4037-4041
Number of pages	5
Journal	Tetrahedron Letters
Volume	50
Issue number	28
DOIs	https://doi.org/10.1016/j.tetlet.2009.04.064
Publication status	Published - 2009 Jul 15

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

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10.1016/j.tetlet.2009.04.064

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title = "Novel synthesis of indolylquinoline derivatives via the C-alkylation of Baylis-Hillman adducts",

abstract = "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 described.",

author = "Chintakunta Ramesh and Veerababurao Kavala and Raju, \{B. Rama\} and Kuo, \{Chun Wei\} and Yao, \{Ching Fa\}",

note = "Funding Information: Financial support for this work by the National Science Council of the Republic of China and National Taiwan Normal University (TOP001) is gratefully acknowledged.",

year = "2009",

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doi = "10.1016/j.tetlet.2009.04.064",

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T1 - Novel synthesis of indolylquinoline derivatives via the C-alkylation of Baylis-Hillman adducts

AU - Ramesh, Chintakunta

AU - Kavala, Veerababurao

AU - Raju, B. Rama

AU - Kuo, Chun Wei

AU - Yao, Ching Fa

N1 - Funding Information: Financial support for this work by the National Science Council of the Republic of China and National Taiwan Normal University (TOP001) is gratefully acknowledged.

PY - 2009/7/15

Y1 - 2009/7/15

N2 - 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 described.

AB - 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 described.

UR - https://www.scopus.com/pages/publications/66149085238

UR - https://www.scopus.com/pages/publications/66149085238#tab=citedBy

U2 - 10.1016/j.tetlet.2009.04.064

DO - 10.1016/j.tetlet.2009.04.064

M3 - Article

AN - SCOPUS:66149085238

SN - 0040-4039

VL - 50

SP - 4037

EP - 4041

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 28

ER -

Novel synthesis of indolylquinoline derivatives via the C-alkylation of Baylis-Hillman adducts

Abstract

ASJC Scopus subject areas

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CCDC 714386: Experimental Crystal Structure Determination

CCDC 714387: Experimental Crystal Structure Determination

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Novel synthesis of indolylquinoline derivatives via the C-alkylation of Baylis-Hillman adducts

Abstract

ASJC Scopus subject areas

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Datasets

CCDC 714386: Experimental Crystal Structure Determination

CCDC 714387: Experimental Crystal Structure Determination

Cite this