Literature DB >> 21216172

Sonochemical multi-component synthesis of spirooxindoles.

Minoo Dabiri1, Zeinab Noroozi Tisseh, Mahboobeh Bahramnejad, Ayoob Bazgir.   

Abstract

New and efficient multi-component methods have been developed for the synthesis of spirooxindoles in the presence of a catalytic amount of p-TSA as an inexpensive and available catalyst in EtOH under ultrasound irradiation. The method is simple, starts from readily accessible commercial starting materials, and provides biologically interesting products in good yields and short reaction times.
Copyright © 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 21216172     DOI: 10.1016/j.ultsonch.2010.12.004

Source DB:  PubMed          Journal:  Ultrason Sonochem        ISSN: 1350-4177            Impact factor:   7.491


  5 in total

Review 1.  Advancements in tetronic acid chemistry. Part 2: Use as a simple precursor to privileged heterocyclic motifs.

Authors:  Moaz M Abdou; Rasha A El-Saeed; Khaled M Elattar; Zeynel Seferoğlu; John Boukouvalas
Journal:  Mol Divers       Date:  2016-06-27       Impact factor: 2.943

Review 2.  Sonochemical Protocols for Heterocyclic Synthesis: A Representative Review.

Authors:  Meena Devi; Rahul Singh; Jayant Sindhu; Ashwani Kumar; Sohan Lal; Ramesh Kumar; Khalid Hussain; Megha Sachdeva; Devender Singh; Parvin Kumar
Journal:  Top Curr Chem (Cham)       Date:  2022-02-12

3.  Catalyst-free synthesis of acenaphthoindolopyrimidine derivatives.

Authors:  Nahale Kakavand; Mohammad Bayat; Yadollah Bayat
Journal:  Mol Divers       Date:  2022-09-20       Impact factor: 3.364

4.  One-pot, sequential four-component synthesis of novel heterocyclic [3.3.3] propellane derivatives at room temperature.

Authors:  Maryam Beyrati; Alireza Hasaninejad
Journal:  RSC Adv       Date:  2018-04-17       Impact factor: 4.036

5.  Synthesis of spiro[dihydropyridine-oxindoles] via three-component reaction of arylamine, isatin and cyclopentane-1,3-dione.

Authors:  Yan Sun; Jing Sun; Chao-Guo Yan
Journal:  Beilstein J Org Chem       Date:  2013-01-03       Impact factor: 2.883

  5 in total

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