Title of article :
The asymmetric aminohydroxylation route to GABOB and homoserine derivatives
Author/Authors :
Michael Harding، نويسنده , , Jennifer A. Bodkin، نويسنده , , Fatiah Issa، نويسنده , , Craig A. Hutton، نويسنده , , Anthony C. Willis، نويسنده , , Malcolm D. McLeod، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2009
Pages :
13
From page :
831
To page :
843
Abstract :
The 4-nitrophenyl ether is an efficient directing group in the asymmetric aminohydroxylation reaction of homoallylic ether derivatives. Either regioisomeric product can be obtained with useful levels of enantioselectivity allowing for the short enantioselective synthesis of GABOB and homoserine derivatives. A model based on substrate-catalyst interactions is presented to explain the regio- and enantioselectivity of the aminohydroxylation reactions.
Keywords :
Osmium , Asymmetric catalysis , Regioselective , Amino acid , Asymmetric aminohydroxylation
Journal title :
Tetrahedron
Serial Year :
2009
Journal title :
Tetrahedron
Record number :
1095033
Link To Document :
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