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https://dspace.iiti.ac.in/handle/123456789/9351
| Title: | Meso enamine substituted BODIPYs |
| Authors: | Mobin, Shaikh M. Misra, Rajneesh |
| Keywords: | aliphatic amine;alkyl group;carbon;deoxyribodipyrimidine photolyase;enamine;hydrogen;nitrogen;article;catalyst;crystal structure;optics;oxidation;position;substitution reaction |
| Issue Date: | 2014 |
| Citation: | Dhokale, B., Jadhav, T., Mobin, S. M., & Misra, R. (2014). Meso enamine substituted BODIPYs. Chemical Communications, 50(65), 9119-9121. doi:10.1039/c4cc03857f |
| Abstract: | Different enamines were introduced at the meso position of the BODIPY by catalyst free oxidation of tert-amines and in situ cross coupling with 8-chloro BODIPY. The reaction conditions were optimized to achieve better yields. The reaction works well with aliphatic tert-amines bearing an N-(CH–CH–) backbone. The N-alkyl substituents perturb the optical properties of enamine substituted BODIPYs. © 2014 The Royal Society of Chemistry. |
| URI: | https://doi.org/10.1039/c4cc03857f https://dspace.iiti.ac.in/handle/123456789/9351 |
| ISSN: | 1359-7345 |
| Type of Material: | Journal Article |
| Appears in Collections: | Department of Chemistry |
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