Title of article :
A new diorganozinc-based enantioselective access to truncated d-ribo-phytosphingosine
Author/Authors :
Ayad، نويسنده , , Tahar and Génisson، نويسنده , , Yves and Verdu، نويسنده , , Alexandre and Baltas، نويسنده , , Michel and Gorrichon، نويسنده , , Liliane، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2003
Pages :
4
From page :
579
To page :
582
Abstract :
The use of a trans α,β-epoxyaldehyde as a precursor of d-ribo-phytosphingosines was studied. The highly stereoselective alkylation of the aldehyde with a diorganozinc reagent was ensured through double asymmetric induction. The regioselective opening of the epoxide in turn gives access to an azide from which a C10 phytosphingosine can be easily prepared.
Keywords :
Phytosphingosine , diorganozinc reagent , Double asymmetric induction
Journal title :
Tetrahedron Letters
Serial Year :
2003
Journal title :
Tetrahedron Letters
Record number :
1660163
Link To Document :
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