Stereocontrolled Synthesis of 5α- and 5β-Substituted Kainic Acids
- 26 May 1999
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 64 (12) , 4304-4314
- https://doi.org/10.1021/jo982109j
Abstract
No abstract availableKeywords
This publication has 44 references indexed in Scilit:
- Stereocontrolled Synthesis of 4-Substituted (±)-Kainic AcidsThe Journal of Organic Chemistry, 1998
- The role of the C-4 side chain of kainate and dihydrokainate in EAA receptor and transporter selectivityBioorganic & Medicinal Chemistry Letters, 1996
- A Versatile Approach to Acromelic Acid AnaloguesTetrahedron Letters, 1995
- Diastereoselective functionalization of 5-hydroxy prolinates by tandem Horner-Emmons-Michael reactionTetrahedron Letters, 1994
- Enantioselective Synthesis of Novel Functionalised Prolines via [3 + 2] Cycloadditions of a Chiral Azomethine YlidSynlett, 1994
- Synthesis of the ω-phosphonic acid analogue of kainic acidBioorganic & Medicinal Chemistry Letters, 1992
- Configurational variants of hydroxyphenylkainoid: their potent depolarizing activities in the rat central nervous systemBioorganic & Medicinal Chemistry Letters, 1992
- Intermolecular Stereoselective Alkenylation of Chiral N-Acylpyrrolidinium Ions.Acta Chemica Scandinavica, 1992
- Trans-2-carboxy-3-pyrrolidineacetic acid (CPAA), a novel agonist at NMDA-type receptorsNeuroscience Letters, 1988
- A dipeptide derived from kainic and L-glutamic acids: a selective antagonist of amino acid induced neuroexcitation with anticonvulsant propertiesJournal of Medicinal Chemistry, 1985