<p>Construction of spiropyrans <em>via</em> [4+2] photocycloaddition reactions and its computational investigation</p>
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Title Statement |
<p>Construction of spiropyrans <em>via</em> [4+2] photocycloaddition reactions and its computational investigation</p> |
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Added Entry - Uncontrolled Name |
singh, saurabh ; MDS, university, Ajmer, Rajasthan Joshi, Rahul ; Department of Chemistry, University of Rajasthan, Jaipur 302 055, India Pardasani, R T ; School of Chemical Sciences and Pharmacy, Central University of Rajasthan, Bandarsindri, Ajmer 305 801, India |
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Uncontrolled Index Term |
Chalones, 2-Chloropropene, DFT-B3LYP/6-31-G+ (2d,2p), Heteroary ketones, Thioisatin |
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Summary, etc. |
<p><strong>Abstract </strong></p> <p>[4+2]-Photochemical cycloaddition provides one of the most efficient and versatile route for the exploring of carbocyclic and heterocyclic frameworks of different sizes with high atom economy. [4+2] photocycloaddition of the chalcones <strong>(2a-h)</strong> obtained by Knoevenagel condensation of thiosatin and different heteroaryl ketones <em>viz.</em> 2-acetyl, 3-acetyl, 4-acetylpyridines and 2-acetylthiophene olefinic 2-chloropropene with as dienophiles led to the construction of six membered novel spiropyran heterocycles (<strong>3a-h</strong>) with 60% yield. The mechanism of the [4+2] photocycloaddition reaction has been investigated in detail by DFT-B3LYP/6-31-G+ (2d, 2p) computational method.<strong></strong></p><br /> |
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Publication, Distribution, Etc. |
Indian Journal of Chemistry -Section B (IJC-B) 2020-11-09 10:52:30 |
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Electronic Location and Access |
application/pdf http://op.niscair.res.in/index.php/IJCB/article/view/28148 |
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Data Source Entry |
Indian Journal of Chemistry -Section B (IJC-B); ##issue.vol## 59, ##issue.no## 8 (2020): Indian Journal of Chemistry Section - B (IJCB) |
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Language Note |
en |
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