Issue 91, 2016

Metal-free 1,3-dipolar cycloaddition approach towards the regioselective synthesis of β-carboline and isoxazole based molecular hybrids

Abstract

Nature has nourished β-carboline and isoxazole derivatives as privileged scaffolds and consequently they are ubiquitously found in alkaloids isolated from various sources. Moreover, several drug molecules based on them have been released in the market. Considering their immense impact, novel β-carboline–isoxazole-based molecular hybrids have been designed and a 1,3-dipolar cycloaddition strategy was devised to prepare the desired prototypes. A library of compounds with a wide range of diversity have been developed by employing β-carboline-containing dipolarophiles as well as dipoles. The current method represents a simple, efficient and easy-to-execute protocol towards the regioselective synthesis of β-carboline–isoxazole conjugates.

Graphical abstract: Metal-free 1,3-dipolar cycloaddition approach towards the regioselective synthesis of β-carboline and isoxazole based molecular hybrids

Supplementary files

Article information

Article type
Paper
Submitted
18 ⵢⵓⵏ 2016
Accepted
29 ⵖⵓⵛ 2016
First published
30 ⵖⵓⵛ 2016

RSC Adv., 2016,6, 88066-88076

Metal-free 1,3-dipolar cycloaddition approach towards the regioselective synthesis of β-carboline and isoxazole based molecular hybrids

D. Singh, N. Devi, V. Kumar, C. C. Malakar, S. Mehra, R. K. Rawal, B. S. Kaith and V. Singh, RSC Adv., 2016, 6, 88066 DOI: 10.1039/C6RA15875G

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