A convenient method of synthesis of bisindolylmethanes: Indium trichloride catalyzed reactions of indole with aldehydes and Schiff's bases

Govindarajulu Babu; Nimmagadda Sridhar; Paramasivan T. Perumal

doi:10.1080/00397910008087197

A convenient method of synthesis of bisindolylmethanes: Indium trichloride catalyzed reactions of indole with aldehydes and Schiff's bases

Govindarajulu Babu, Nimmagadda Sridhar, Paramasivan T. Perumal

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

213 Scopus citations

Abstract

Anhydrous indium trichloride (InCl₃) is found to catalyze the electrophilic substitution reaction of indole with aromatic aldehydes and Schiff's bases which resulted in an efficient synthesis of bis- indolylmethanes in good to excellent yield.

Original language	English (US)
Pages (from-to)	1609-1614
Number of pages	6
Journal	Synthetic Communications
Volume	30
Issue number	9
DOIs	https://doi.org/10.1080/00397910008087197
State	Published - 2000
Externally published	Yes

ASJC Scopus subject areas

Organic Chemistry

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10.1080/00397910008087197

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title = "A convenient method of synthesis of bisindolylmethanes: Indium trichloride catalyzed reactions of indole with aldehydes and Schiff's bases",

abstract = "Anhydrous indium trichloride (InCl3) is found to catalyze the electrophilic substitution reaction of indole with aromatic aldehydes and Schiff's bases which resulted in an efficient synthesis of bis- indolylmethanes in good to excellent yield.",

author = "Govindarajulu Babu and Nimmagadda Sridhar and Perumal, {Paramasivan T.}",

year = "2000",

doi = "10.1080/00397910008087197",

language = "English (US)",

volume = "30",

pages = "1609--1614",

journal = "Synthetic Communications",

issn = "0039-7911",

publisher = "Taylor and Francis Ltd.",

number = "9",

}

TY - JOUR

T1 - A convenient method of synthesis of bisindolylmethanes

T2 - Indium trichloride catalyzed reactions of indole with aldehydes and Schiff's bases

AU - Babu, Govindarajulu

AU - Sridhar, Nimmagadda

AU - Perumal, Paramasivan T.

PY - 2000

Y1 - 2000

N2 - Anhydrous indium trichloride (InCl3) is found to catalyze the electrophilic substitution reaction of indole with aromatic aldehydes and Schiff's bases which resulted in an efficient synthesis of bis- indolylmethanes in good to excellent yield.

AB - Anhydrous indium trichloride (InCl3) is found to catalyze the electrophilic substitution reaction of indole with aromatic aldehydes and Schiff's bases which resulted in an efficient synthesis of bis- indolylmethanes in good to excellent yield.

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U2 - 10.1080/00397910008087197

DO - 10.1080/00397910008087197

M3 - Article

AN - SCOPUS:0034040349

SN - 0039-7911

VL - 30

SP - 1609

EP - 1614

JO - Synthetic Communications

JF - Synthetic Communications

IS - 9

ER -

A convenient method of synthesis of bisindolylmethanes: Indium trichloride catalyzed reactions of indole with aldehydes and Schiff's bases

Abstract

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