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Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.1c04359
Abstract: The gem-difluoroalkene moiety is an ideal carbonyl bioisostere in medicinal chemistry, but efficient synthesis of β-gem-difluoroalkene esters remains challenging so far. Herein, we disclose a photoredox-catalyzed allylic defluorinative alkoxycarbonylation of trifluoromethyl alkenes enabled by intermolecular…
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Keywords:
allylic defluorinative;
defluorinative alkoxycarbonylation;
alkoxycarbonylation trifluoromethyl;
catalyzed allylic ... See more keywords
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Published in 2020 at "Synlett"
DOI: 10.1055/s-0040-1707170
Abstract: We report a reductive allylic defluorinative reaction of α-trifluoromethyl alkenes with terminal epoxides, which consists of an iodide-mediated regioselective ring opening and a nickel-catalyzed radical-type cross-coupling, providing diverse tertiary gem-difluorobishomoallylic alcohols in moderate to high…
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Keywords:
trifluoromethyl alkenes;
allylic defluorinative;
reductive allylic;
nickel catalyzed ... See more keywords