Title of article :
Synthesis of optically active β-alkyl aspartate via [3,3] sigmatropic rearrangement of α-acyloxytrialkylsilane
Author/Authors :
Sakaguchi، نويسنده , , Kazuhiko and Yamamoto، نويسنده , , Masahiro and Kawamoto، نويسنده , , Tetsuo and Yamada، نويسنده , , Takeshi and Shinada، نويسنده , , Tetsuro and Shimamoto، نويسنده , , Keiko and Ohfune، نويسنده , , Yasufumi، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2004
Pages :
4
From page :
5869
To page :
5872
Abstract :
The synthesis of four types of optically active β-carbon-substituted analogs of threo-β-hydroxy aspartate (THA) and a β-carbon-substituted analog of threo-β-benzyloxy aspartate (TBOA), which are potent blockers of excitatory amino acid transporters in the mammalian central nervous system, via the chirality-transferring ester–enolate Claisen rearrangement of α-acyloxytrialkylsilane is described.
Keywords :
threo-?-Hydroxy aspartate , Glutamate transporter , ?-Acyloxysilane , threo-?-Benzyloxy aspartate , Ester–enolate Claisen rearrangement , ?-hydroxysilane
Journal title :
Tetrahedron Letters
Serial Year :
2004
Journal title :
Tetrahedron Letters
Record number :
1842781
Link To Document :
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