Catalyst-free aqueous-mediated conjugative addition of indoles to β-nitrostyrenes

Pateliya Mujjamil Habib; Veerababurao Kavala; Chun Wei Kuo; Ching Fa Yao

doi:10.1016/j.tetlet.2008.09.109

Catalyst-free aqueous-mediated conjugative addition of indoles to β-nitrostyrenes

Pateliya Mujjamil Habib, Veerababurao Kavala, Chun Wei Kuo, Ching Fa Yao

Department of Chemistry

Research output: Contribution to journal › Article

53 Citations (Scopus)

Abstract

A catalyst free aqueous-mediated alkylation of indoles with various β-nitrostyrenes was performed at elevated temperature. No catalyst, clean reaction conditions, simple workup procedure, easy isolation, viability for large scale preparation, and environmentally acceptable medium are the best features in this process.

Original language	English
Pages (from-to)	7005-7007
Number of pages	3
Journal	Tetrahedron Letters
Volume	49
Issue number	49
DOIs	https://doi.org/10.1016/j.tetlet.2008.09.109
Publication status	Published - 2008 Dec 1

ASJC Scopus subject areas

Biochemistry
Drug Discovery
Organic Chemistry

Access to Document

10.1016/j.tetlet.2008.09.109

Fingerprint Dive into the research topics of 'Catalyst-free aqueous-mediated conjugative addition of indoles to β-nitrostyrenes'. Together they form a unique fingerprint.

Cite this

Habib, P. M., Kavala, V., Kuo, C. W., & Yao, C. F. (2008). Catalyst-free aqueous-mediated conjugative addition of indoles to β-nitrostyrenes. Tetrahedron Letters, 49(49), 7005-7007. https://doi.org/10.1016/j.tetlet.2008.09.109

@article{6c7e040a1d584b92a47464b611c0655d,

title = "Catalyst-free aqueous-mediated conjugative addition of indoles to β-nitrostyrenes",

abstract = "A catalyst free aqueous-mediated alkylation of indoles with various β-nitrostyrenes was performed at elevated temperature. No catalyst, clean reaction conditions, simple workup procedure, easy isolation, viability for large scale preparation, and environmentally acceptable medium are the best features in this process.",

author = "Habib, {Pateliya Mujjamil} and Veerababurao Kavala and Kuo, {Chun Wei} and Yao, {Ching Fa}",

year = "2008",

month = dec,

day = "1",

doi = "10.1016/j.tetlet.2008.09.109",

language = "English",

volume = "49",

pages = "7005--7007",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "49",

}

TY - JOUR

T1 - Catalyst-free aqueous-mediated conjugative addition of indoles to β-nitrostyrenes

AU - Habib, Pateliya Mujjamil

AU - Kavala, Veerababurao

AU - Kuo, Chun Wei

AU - Yao, Ching Fa

PY - 2008/12/1

Y1 - 2008/12/1

N2 - A catalyst free aqueous-mediated alkylation of indoles with various β-nitrostyrenes was performed at elevated temperature. No catalyst, clean reaction conditions, simple workup procedure, easy isolation, viability for large scale preparation, and environmentally acceptable medium are the best features in this process.

AB - A catalyst free aqueous-mediated alkylation of indoles with various β-nitrostyrenes was performed at elevated temperature. No catalyst, clean reaction conditions, simple workup procedure, easy isolation, viability for large scale preparation, and environmentally acceptable medium are the best features in this process.

UR - http://www.scopus.com/inward/record.url?scp=54049093542&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=54049093542&partnerID=8YFLogxK

U2 - 10.1016/j.tetlet.2008.09.109

DO - 10.1016/j.tetlet.2008.09.109

M3 - Article

AN - SCOPUS:54049093542

VL - 49

SP - 7005

EP - 7007

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 49

ER -