Abstract
A library of hitherto unknown functionalized and annulated spiro[indoline-3,1`-indolizin]-2-one derivatives incorporating thiophene moiety has been synthesized under conventional and microwave irradiation conditions. The structures, regio and diastereoselectivity of the synthesized cycloadducts have been confirmed using different analytical and spectral tools.
Keywords: 2d NMR, microwave irradiation, regioselectivity, spiro[indoline-3, 1`-indolizin]-2-one derivatives.
Letters in Organic Chemistry
Title:Microwave-mediated Regiospecific Synthesis of Some Novel Annulated Spiro[indoline-3,1`-indolizin]-2-ones
Volume: 12 Issue: 1
Author(s): Abdullah S. Al-Bogami and Abdelaziz S. El-Ahl
Affiliation:
Keywords: 2d NMR, microwave irradiation, regioselectivity, spiro[indoline-3, 1`-indolizin]-2-one derivatives.
Abstract: A library of hitherto unknown functionalized and annulated spiro[indoline-3,1`-indolizin]-2-one derivatives incorporating thiophene moiety has been synthesized under conventional and microwave irradiation conditions. The structures, regio and diastereoselectivity of the synthesized cycloadducts have been confirmed using different analytical and spectral tools.
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Cite this article as:
Al-Bogami S. Abdullah and El-Ahl S. Abdelaziz, Microwave-mediated Regiospecific Synthesis of Some Novel Annulated Spiro[indoline-3,1`-indolizin]-2-ones, Letters in Organic Chemistry 2015; 12 (1) . https://dx.doi.org/10.2174/1570178611666141016215558
DOI https://dx.doi.org/10.2174/1570178611666141016215558 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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