Synthesis of the four d,l-pairs of 2-amino-3-phenylnorbornane-2-carboxylic acids II. The use of 5(4H)-oxazolones as dienophiles.
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference25 articles.
1. A Bicyclic Amino Acid to Improve Discriminations among Transport Systems
2. Behavior in the Rat of a Transport-specific, Bicyclic Amino Acid
3. 2-Aminonorbornane-2-carboxylic acid. Preparation, properties, and identification of the four isomers
4. A synthesis of 2-aminonorbornene-2-carboxylic acid derivatives by diels-alder reaction using α,β-dehydroalaninates as a dienophile
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1. Hydroarylation of Substituted Norbornene Amino Acids: Studies on Long-Range Stereo-Electronic Effects on the Regioselectivity of the Addition;Current Organic Chemistry;2012-11-01
2. Regioselective 1,3-dipolar cycloaddition of phenanthrolinium N-ylides to substituted arylidene oxazolones;Molecular Diversity;2011-03-22
3. ChemInform Abstract: Synthesis of the Four d,l-Pairs of 2-Amino-3-phenylnorbornane-2- carboxylic Acids. Part 2. The Use of 5(4H)-Oxazolones as Dienophiles.;ChemInform;2010-08-20
4. Uncatalyzed solventless Diels–Alder reaction of 2-amino-3-nitroacrylate: synthesis of new epimeric 2-amino-3-nitro-norbornene- and norbornane-2-carboxylic acids;Tetrahedron;2006-02
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