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Enantioselective synthesis of α-perfluoroalkylated prolines, their 6,7-membered homologues and derivatives. | LitMetric

Enantioselective synthesis of α-perfluoroalkylated cyclic amino acids and their derivatives was elaborated using the organocatalytic Strecker reaction with 5-7 membered cyclic ketimines. The prepared amino nitriles could be transformed into chiral Rf-prolines and their 6,7-membered homologues as well as their corresponding amides and diamines (yields up to 99%, up to >99% ee).

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http://dx.doi.org/10.1039/c8ob01223gDOI Listing

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