Metal-Free Ammonia Borane-Catalyzed Hydroboration of Lactones and Esters to Alcohols

dc.contributor.authorYessengazin, Azamat
dc.contributor.authorSeisenkul, Bakdaulet
dc.contributor.authorTusupbayev, Samat
dc.contributor.authorAndizhanova, Tolganay
dc.contributor.authorKhalimon, Andrey
dc.contributor.institutionDepartment of Chemistry, School of Sciences and Humanities, Nazarbayev University
dc.date.accessioned2025-07-02T06:45:45Z
dc.date.available2025-07-02T06:45:45Z
dc.date.issued2024
dc.description.abstractHerein we describe an efficient methodology for metal-free hydroborative cleavage of lactones and esters with HBPin (Pin =pinacol) to the corresponding alcohol derivatives using ammonia borane as a pre-catalyst. The reactions proceed under mild conditions, can be performed in a solvent-free manner, and do not require an inert atmosphere. Combined experimental and computational mechanistic studies suggest a novel mechanism that involves μ-aminodiboranes as catalytically active species.
dc.format.mediumPDF
dc.identifier.citationYessengazin, A., Seisenkul, B., Tussupbayev, S., Andizhanova, T., & Khalimon, A. Y. (2024). Metal‐Free Ammonia Borane‐Catalyzed Hydroboration of Lactones and Esters to Alcohols. ChemCatChem, 16(20), e202400876. https://doi.org/10.1002/cctc.202400876
dc.identifier.issn1867-3880
dc.identifier.urihttps://doi.org/10.1002/cctc.202400876
dc.identifier.urihttps://nur.nu.edu.kz/handle/123456789/9043
dc.language.isoen
dc.publisherWiley
dc.rightsCC BY-NCen
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/
dc.sourceChemCatChem, 16(20), e202400876
dc.subjectNU-Wiley transformative agreement
dc.subjectMetal‐Free Ammonia
dc.subjectμ-aminodiboranes
dc.subjectHBPin (Pin =pinacol)
dc.titleMetal-Free Ammonia Borane-Catalyzed Hydroboration of Lactones and Esters to Alcohols
dc.typeArticle
person.identifier.orcidhttps://orcid.org/0000-0003-2156-8810
project.funder.nameNazarbayev University

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