Title of article :
Stereoselective synthesis of trans-disubstituted-β-lactams from N-phenylsulfenylimines
Author/Authors :
Coantic، نويسنده , , Stéphanie and Mouysset، نويسنده , , Dominique and Mignani، نويسنده , , Serge and Tabart، نويسنده , , Michel and Stella، نويسنده , , Lucien، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2007
Pages :
3
From page :
4301
To page :
4303
Abstract :
N-Phenylsulfenylimines derived from aliphatic, aromatic and heteroaromatic aldehydes act as nucleophilic partners in the Staudinger reaction with acetoxyacetyl chloride. Disubstituted-β-lactams are obtained with a surprisingly high trans diastereoselection (up to 99%).
Keywords :
N-Sulfenylimines , Staudinger reaction , N-Thiolated-trans-?-lactams
Journal title :
Tetrahedron Letters
Serial Year :
2007
Journal title :
Tetrahedron Letters
Record number :
1855232
Link To Document :
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