Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/14911
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dc.contributor.authorChillal, Abhinay Subodhen_US
dc.contributor.authorMaurya, Chandanien_US
dc.contributor.authorKshirsagar, Umesh Achyutraoen_US
dc.date.accessioned2024-12-18T10:34:08Z-
dc.date.available2024-12-18T10:34:08Z-
dc.date.issued2024-
dc.identifier.citationChillal, 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.4c03052en_US
dc.identifier.issn0743-7463-
dc.identifier.otherEID(2-s2.0-85207013034)-
dc.identifier.urihttps://doi.org/10.1021/acs.langmuir.4c03052-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/14911-
dc.description.abstractAn 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.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.sourceLangmuiren_US
dc.titleMicelle-Assisted C(sp2)-H Functionalization for C-Se and C-X Bond Formation in the Aqueous Mediumen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

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