Synthesis of enantiopure azetidines: a route to new β-amino alcohols |
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| Authors: | Vincent Lemau de Talancé ,Catherine Kadouri-Puchot |
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| Affiliation: | Laboratoire de Chimie Organique-Equipe Synthèse Asymétrique, UMR 7611, Institut de Chimie Moléculaire FR 2769, Université Pierre et Marie Curie, 4 place jussieu, 75005 Paris, France |
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| Abstract: | β-Amino alcohols possessing an E vinylsilane moiety were cyclized in the presence of N-bromosuccinimide to afford diastereoisomerically pure polyfunctional azetidines. These azetidines were then transformed into enantiopure β-amino alcohols with a Z vinylic bromide moiety. |
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| Keywords: | Azetidines β-Amino alcohols N-Bromosuccinimide Vinylsilane Vinylbromide |
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