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Dipolar cycloaddition based multi-component reaction: Synthesis of spiro tethered acenaphthylene-indolizine-pyridinone hybrids
Journal article   Peer reviewed

Dipolar cycloaddition based multi-component reaction: Synthesis of spiro tethered acenaphthylene-indolizine-pyridinone hybrids

Raju Suresh Kumar, Abdulrahman I. Almansour, Natarajan Arumugam, Govindasami Periyasami, S. Athimoolam, Raju Ranjith Kumar, Mohammad Asad and Abdullah M. Asiri
Tetrahedron letters, Vol.59(35), pp.3336-3340
29/08/2018
DOI: https://doi.org/10.1016/j.tetlet.2018.07.051

Abstract

Chemistry Chemistry, Organic Physical Sciences Science & Technology
The stereoselective syntheses of novel dispiro acenaphthylene-indolizine-pyridinone hybrid heterocycles have been achieved through one-pot four-component domino 1,3-dipolar cycloaddition-Michael addition-air oxidation sequence of reactions. (C) 2018 Elsevier Ltd. All rights reserved.

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