Intramolecular Diels-Alder route to 6-oxodecahydroisoquinoline-3-carboxylates: Intermediates for the synthesis of conformationally constrained excitatory amino acid antagonists
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. 6-Substituted decahydroisoquinoline-3-carboxylic acids as potent and selective conformationally constrained NMDA receptor antagonists
2. (3SR,4aRS,6RS,8aRS)-6-[2-(1H-Tetrazol-5-yl)ethyl]decahydroisoquinoline-3-carboxylic acid: a structurally novel, systemically active, competitive AMPA receptor antagonist
3. Unusual stereochemical preferences of decahydroisoquinoline-3-cargoxylic acid competitive NMDA antagonists
4. Syntheses of 6-oxodecahydroisoquinoline-3-carboxylates. Useful intermediates for the preparation of conformationally defined excitatory amino acid antagonists
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1. A detailed study of the diastereoselective catalytic hydrogenation of 6-hydroxytetrahydroisoquinoline-(3R)-carboxylic ester intermediates;Catalysis Science & Technology;2012
2. ChemInform Abstract: Intramolecular Diels-Alder Route to 6-Oxodecahydroisoquinoline-3-carboxylates: Intermediates for the Synthesis of Conformationally Constrained Excitatory Amino Acid Antagonists.;ChemInform;2010-08-18
3. Methyl (S)-2-Phthalimido-4-Oxobutanoate;Organic Syntheses;2003-04-28
4. Asymmetric Synthesis of 2-Amino-3-hydroxynorbornene-2-carboxylic Acid Derivatives;The Journal of Organic Chemistry;2001-08-24
5. Stereoselective synthesis of allyl- and homoallylglycines;Tetrahedron Letters;2001-05
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