Title of article :
1,3-Rearrangement of ketene-N,O-acetals
Author/Authors :
Suzuki، نويسنده , , Tatsuo and Inui، نويسنده , , Masaharu and Hosokawa، نويسنده , , Seijiro and Kobayashi، نويسنده , , Susumu، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2003
Pages :
4
From page :
3713
To page :
3716
Abstract :
Ketene N,O-acetals were prepared stereoselectively and submitted to a Lewis acid-mediated 1,3-rearrangement to afford C-alkylated products. The reactions proceeded in a stereoselective manner to construct a chiral quaternary carbon in high selectivity. The stereochemistry of the quaternary center was found to be opposite to that obtained by an anionic direct dienolate alkylation.
Journal title :
Tetrahedron Letters
Serial Year :
2003
Journal title :
Tetrahedron Letters
Record number :
1662016
Link To Document :
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