Abstract
A highly efficient and environmentally benign reaction of dimedone with various aldehydes and Narylthioureas to afford monastrol analogues is revealed. The reaction is found to be sensitive towards the steric and electronic effects of the substituents in variable components. A quantitative optimization of catalytic support is also presented.
Keywords: Monastrol, microwaves, multicomponent reactions, electronic and steric effects
Letters in Organic Chemistry
Title: Microwave Accelerated Multicomponent Synthesis for a Novel Scaffold of Monastrol Analogues
Volume: 4 Issue: 5
Author(s): Mazaahir Kidwai, Suchi Kukreja, Shewta Rastogi and Kavita Singhal
Affiliation:
Keywords: Monastrol, microwaves, multicomponent reactions, electronic and steric effects
Abstract: A highly efficient and environmentally benign reaction of dimedone with various aldehydes and Narylthioureas to afford monastrol analogues is revealed. The reaction is found to be sensitive towards the steric and electronic effects of the substituents in variable components. A quantitative optimization of catalytic support is also presented.
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Cite this article as:
Mazaahir Kidwai , Suchi Kukreja , Shewta Rastogi and Kavita Singhal , Microwave Accelerated Multicomponent Synthesis for a Novel Scaffold of Monastrol Analogues, Letters in Organic Chemistry 2007; 4 (5) . https://dx.doi.org/10.2174/157017807781212085
DOI https://dx.doi.org/10.2174/157017807781212085 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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