Direct asymmetric bromination of aldehydes catalyzed by a binaphthyl-based secondary amine: highly enantio- and diastereoselective one-pot synthesis of bromohydrins

One-pot stereoselective synthesis of bromohydrins as a useful chiral building block was achieved by the reaction of Grignard reagents with optically active α-bromoaldehydes, which were in situ generated by direct asymmetric bromination of aldehydes catalyzed by a binaphthyl-based secondary amine (S)...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2010-10, Vol.46 (40), p.7590-7592
Hauptverfasser: Kano, Taichi, Shirozu, Fumitaka, Maruoka, Keiji
Format: Artikel
Sprache:eng
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Zusammenfassung:One-pot stereoselective synthesis of bromohydrins as a useful chiral building block was achieved by the reaction of Grignard reagents with optically active α-bromoaldehydes, which were in situ generated by direct asymmetric bromination of aldehydes catalyzed by a binaphthyl-based secondary amine (S)-3.
ISSN:1359-7345
1364-548X
DOI:10.1039/c0cc02739a