Catalyst free synthesis of α-fluoro-β-hydroxy ketones/α-fluoro-ynols via electrophilic fluorination of tertiary propargyl alcohols using Selectfluor™ (F-TEDA-BF < inf > 4 < /inf > )

dc.contributor.author Naveen, Naganaboina
dc.contributor.author Balamurugan, Rengarajan
dc.date.accessioned 2022-03-27T08:39:11Z
dc.date.available 2022-03-27T08:39:11Z
dc.date.issued 2017-01-01
dc.description.abstract A facile method for the synthesis of α-fluoro-β-hydroxy ketones/α-fluoro-ynols from tertiary propargyl alcohols under electrophilic fluorination conditions using F-TEDA-BF4 has been presented. The products bear pharmaceutically important α-fluoro ketone, gem-diaryl and fluorohydrin moieties in the same molecule. Interestingly, this catalyst free protocol results in monofluorination.
dc.identifier.citation Organic and Biomolecular Chemistry. v.15(9)
dc.identifier.issn 14770520
dc.identifier.uri 10.1039/c7ob00140a
dc.identifier.uri http://xlink.rsc.org/?DOI=C7OB00140A
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/11372
dc.title Catalyst free synthesis of α-fluoro-β-hydroxy ketones/α-fluoro-ynols via electrophilic fluorination of tertiary propargyl alcohols using Selectfluor™ (F-TEDA-BF < inf > 4 < /inf > )
dc.type Journal. Article
dspace.entity.type
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