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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Chillal, Abhinay Subodh | en_US |
dc.contributor.author | Maurya, Chandani | en_US |
dc.contributor.author | Kshirsagar, Umesh Achyutrao | en_US |
dc.date.accessioned | 2024-12-18T10:34:08Z | - |
dc.date.available | 2024-12-18T10:34:08Z | - |
dc.date.issued | 2024 | - |
dc.identifier.citation | Chillal, A. S., Maurya, C., & Kshirsagar, U. A. (2024). Micelle-Assisted C(sp2)-H Functionalization for C-Se and C-X Bond Formation in the Aqueous Medium. Langmuir. Scopus. https://doi.org/10.1021/acs.langmuir.4c03052 | en_US |
dc.identifier.issn | 0743-7463 | - |
dc.identifier.other | EID(2-s2.0-85207013034) | - |
dc.identifier.uri | https://doi.org/10.1021/acs.langmuir.4c03052 | - |
dc.identifier.uri | https://dspace.iiti.ac.in/handle/123456789/14911 | - |
dc.description.abstract | An environmentally sustainable, versatile, and cost-effective approach for C-Se and C-X (X = I, Br, and Cl) bond formation through C-H functionalization assisted by micellar catalysis in water is developed. The reaction utilizes a minimum amount of diorganyl diselenides and potassium halides for the respective functionalizations. The present protocol was suitable for scale-up synthesis, which directly provided the desired selenylated products without the need for chromatographic purification, in sufficient purity. The aqueous micellar catalysis system was reusable for up to 5 reaction cycles without compromising the reaction yield. © 2024 American Chemical Society. | en_US |
dc.language.iso | en | en_US |
dc.publisher | American Chemical Society | en_US |
dc.source | Langmuir | en_US |
dc.title | Micelle-Assisted C(sp2)-H Functionalization for C-Se and C-X Bond Formation in the Aqueous Medium | en_US |
dc.type | Journal Article | en_US |
Appears in Collections: | Department of Chemistry |
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