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Org Lett ; 6(8): 1285-8, 2004 Apr 15.
Article in English | MEDLINE | ID: mdl-15070318

ABSTRACT

Utilizing our lateral metalation coupled with Jacobsen's catalytic asymmetric amino nitrile synthesis, we have demonstrated the ability to synthesize isoxazole-containing amino acid glutamate analogues in high yield and high enantiomeric excesses. Chiral centers alpha or beta at the C-5 position do not detract from diastereoselectivity of the Jacobsen-Strecker reaction. [reaction: see text]


Subject(s)
Glutamates/chemical synthesis , Neurons/drug effects , Neurotransmitter Agents/chemical synthesis , Animals , Binding, Competitive , Brain/metabolism , Catalysis , Glutamates/metabolism , Glutamates/pharmacology , Isoxazoles/chemistry , Mice , Models, Chemical , Neurotransmitter Agents/metabolism , Neurotransmitter Agents/pharmacology , Stereoisomerism , Temperature
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