Generic placeholder image

Letters in Organic Chemistry

Editor-in-Chief

ISSN (Print): 1570-1786
ISSN (Online): 1875-6255

Tandem One-Pot Synthesis of Indoles Having a Structural Moiety of Propellane

Author(s): Abdolali Alizadeh, Fahimeh Bayat and Vahideh Sadeghi

Volume 12, Issue 3, 2015

Page: [153 - 158] Pages: 6

DOI: 10.2174/1570178612666150108003359

Price: $65

Abstract

A concise and efficient route for the synthesis of indole derivatives having propellane structure at position 3 by simple regioselective one-pot reaction of ninhydrin, malononitrile, tryptamine, and β-dicarbonyl compounds was developed. This protocol provides an alternative method for application in combinatorial and parallel synthesis in drug discovery. The value of this method lies in its simplicity, regioselectivity, and good yields. The structures of new synthesized compounds were corroborated spectroscopically (IR, 1H- and 13C-NMR, and EI-MS). A plausible mechanism for this type of reaction is proposed (Scheme 2).

Keywords: Indole, propellane, tryptamin, ninhydrin, one-pot reaction.

Next »
Graphical Abstract


Rights & Permissions Print Cite
© 2024 Bentham Science Publishers | Privacy Policy