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Enantioselective fluorination of α-branched aldehydes and subsequent conversion to α-hydroxyacetals via stereospecific C–F bond cleavage

The highly enantioselective fluorination of α-branched aldehydes was achieved using newly developed chiral primary amine catalyst 1. Furthermore, the C–F bond cleavage of the resulting α-fluoroaldehydes proceeded smoothly under alcoholic alkaline conditions to yield the corresponding α-hydroxyacetal...

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Détails bibliographiques
Publié dans:Chem Sci
Auteurs principaux: Shibatomi, Kazutaka, Kitahara, Kazumasa, Okimi, Takuya, Abe, Yoshiyuki, Iwasa, Seiji
Format: Artigo
Langue:Inglês
Publié: Royal Society of Chemistry 2016
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC5975931/
https://ncbi.nlm.nih.gov/pubmed/29910896
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1039/c5sc03486h
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