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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Mobin, Shaikh M. | en_US |
| dc.contributor.author | Misra, Rajneesh | en_US |
| dc.date.accessioned | 2022-03-17T01:00:00Z | - |
| dc.date.accessioned | 2022-03-21T11:32:29Z | - |
| dc.date.available | 2022-03-17T01:00:00Z | - |
| dc.date.available | 2022-03-21T11:32:29Z | - |
| dc.date.issued | 2014 | - |
| dc.identifier.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 | en_US |
| dc.identifier.issn | 1359-7345 | - |
| dc.identifier.other | EID(2-s2.0-84904548271) | - |
| dc.identifier.uri | https://doi.org/10.1039/c4cc03857f | - |
| dc.identifier.uri | https://dspace.iiti.ac.in/handle/123456789/9351 | - |
| dc.description.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. | en_US |
| dc.language.iso | en | en_US |
| dc.source | Chemical Communications | en_US |
| dc.subject | aliphatic amine | en_US |
| dc.subject | alkyl group | en_US |
| dc.subject | carbon | en_US |
| dc.subject | deoxyribodipyrimidine photolyase | en_US |
| dc.subject | enamine | en_US |
| dc.subject | hydrogen | en_US |
| dc.subject | nitrogen | en_US |
| dc.subject | article | en_US |
| dc.subject | catalyst | en_US |
| dc.subject | crystal structure | en_US |
| dc.subject | optics | en_US |
| dc.subject | oxidation | en_US |
| dc.subject | position | en_US |
| dc.subject | substitution reaction | en_US |
| dc.title | Meso enamine substituted BODIPYs | en_US |
| dc.type | Journal Article | en_US |
| Appears in Collections: | Department of Chemistry | |
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