Synthesis of the four dl-pairs of 2-amino-3-phenylnorbornane-2-carboxylic acids
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference22 articles.
1. Asymmetric synthesis of β-hydroxy-α-alkylamino acids by asymmetric aldol reaction of α-isocyanocarboxylates catalyzed by chiral ferrocenylphosphine-gold(I) complexes
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3. A synthesis of 2-aminonorbornene-2-carboxylic acid derivatives by diels-alder reaction using α,β-dehydroalaninates as a dienophile
4. Diels–Alder reactions of methyl-N-acyl-α,β-dehydroalaninates with cyclopentadiene
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3. Conformationally Constrained Serine Analogues: Synthesis of New 2-Amino-3-hydroxynorbornanecarboxylic Acid Derivatives;The Journal of Organic Chemistry;2000-08-18
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5. Towards control of χ-space: Conformationally constrained analogues of Phe, Tyr, Trp and His;Tetrahedron;1999-01
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