New conditions for the Staudinger reaction provide N-unsubstituted-3-amino-4-substituted-?-lactams in satisfactory yields with complete trans-selectivity and high facial diastereoselectivity.
Highly Enantioselective Synthesis of NH-3-Amino-4-Substituted Azetidin-2-ones via a Two-Step Staudinger Reaction
Bandini E;
1996
Abstract
New conditions for the Staudinger reaction provide N-unsubstituted-3-amino-4-substituted-?-lactams in satisfactory yields with complete trans-selectivity and high facial diastereoselectivity.File in questo prodotto:
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