Title of article :
Synthesis of enantiomerically pure tertiary 1,2-aminoalcohols by the highly diastereoselective reductive ring opening of oxazolidines
Author/Authors :
Philip C. Bulman Page، نويسنده , , Benjamin R. Buckley، نويسنده , , Mark R.J. Elsegood، نويسنده , , Colin M. Hayman، نويسنده , , Harry Heaney، نويسنده , , Gerasimos A. Rassias، نويسنده , , Salem A. Talib، نويسنده , , John Liddle، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2007
Pages :
9
From page :
10991
To page :
10999
Abstract :
A number of enantiomerically pure 1,2-aminoalcohols containing tertiary nitrogen atoms bearing chiral substituents have been prepared by highly diastereoselective reductive ring cleavage of oxazolidines derived from ketones and pseudoephedrine or ephedrine. The ring cleavage occurs with retention of configuration.
Keywords :
Oxazolidine , Aminoalcohol , Reductive cleavage , Enantiomerically pure , Reduction , Stereoselective
Journal title :
Tetrahedron
Serial Year :
2007
Journal title :
Tetrahedron
Record number :
1093369
Link To Document :
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