Diastereoselection in the nucleophilic c
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P. Perlmutter; M. Tabone
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Article
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1988
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Elsevier Science
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French
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Nucleophilic conjugate addition of benzylamine to 2-hydroxyalkylpropenoates la-c proceeds in high yield with modest diastereoselection. However, addition of benxylamine to the silyl ether of lc produces only the anti-isomer 2d in high yield Although nucleophilic conjugate additions of amines to 2-su