Efficient synthesis of optically active α-substituted glutamate analogs possessing α-hydroxymethyl and α-alkoxymethyl groups

Design, Synthesis, and Pharmacological Characterization of (+)-2-Aminobicyclo[3.1.0]hexane-2,6-dicarboxylic Acid (LY354740):  A Potent, Selective, and Orally Active Group 2 Metabotropic Glutamate Receptor Agonist Possessing Anticonvulsant and Anxiolytic Properties

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Pharmacological Characterization, Active Group 2, Psychotropic Medication +16

Synthesis of four diastereomeric L-2-(carboxycyclopropyl)glycines. Conformationally constrained L-glutamate analogs

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Bioorganic Chemistry, Chemical Analysis, Altmetric Attention Score +16

Syntheses and Conformational Analyses of Glutamate Analogs:  2-(2-Carboxy-3-substituted-cyclopropyl)glycines as Useful Probes for Excitatory Amino Acid Receptors

Keiko Shimamoto, Yasufumi Ohfune · Journal of Medicinal Chemistry · 1996 · 111 citations

Total Synthesis and Absolute Structure of Manzacidin A and C

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Absolute Structure, Medicinal Chemistry, Bioorganic Chemistry +14

A useful application of benzyl trichloroacetimidate for the benzylation of alcohols

Peter Eckenberg, Ulrich Groth, Thomas Huhn et al. · Tetrahedron · 1993 · 82 citations

Chemical Engineering, Derivative (Chemistry), Engineering +7