Title of article
Highly stereoselective De-Novo synthesis of protected 2-amino-3-C-methyl-2,3-dideoxy-d-altrose
Author/Authors
Sabine Kollmann، نويسنده , , Elisa Nauha، نويسنده , , Dieter Hoppe، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2010
Pages
5
From page
6162
To page
6166
Abstract
A new strategy for the stereoselective synthesis of 2-amino-2-deoxy-aldoses is described. Therefore epoxy carbamates are reacted with isocyanates to furnish urethanes, which will form the title compounds with high diastereoselectivities under basic conditions and O,O-migration of the carbamoyl group.
Keywords
Branched carbohydrates , O , O-Migration , Urethanes , Isocyanates
Journal title
Tetrahedron
Serial Year
2010
Journal title
Tetrahedron
Record number
1101131
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