Studies on Structure-Activity Relationship of Analgetics. X. Syntheses of 11-Amino-2, 3-benzobicyclo [3. 3. 1] nonane and 3-Phenyl-9-amino-bicyclo [3. 3. 1] nonane Derivatives.
Kemmotsu Mitsuhashi, Shunsaku Shiotani
Abstract
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Kemmotsu Mitsuhashi, Shunsaku Shiotani
Abstract
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Some derivatives of 11-amino-2, 3-benzobicyclo [3. 3. 1] nonane and 3-phenyl-9-amino-bicyclo [3. 3. 1] nonane were synthesized from β-tetralon and 4-phenylcyclohexanone, respectively, through an enamine cyclization. Configuration and conformation of these bicyclic compounds were elucidated by nuclear magnetic resonance spectral analysis. A peculiar property, resembling to Sommelet reaction, of the amino group attached to bridged methylene in bicyclic system is presented. The mass spectra of the amino derivatives of bicyclo [3. 3. 1] nonane system are discussed.
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Some derivatives of 11-amino-2, 3-benzobicyclo [3. 3. 1] nonane and 3-phenyl-9-amino-bicyclo [3. 3. 1] nonane were synthesized from β-tetralon and 4-phenylcyclohexanone, respectively, through an enamine cyclization. Configuration and conformation of these bicyclic compounds were elucidated by nuclear magnetic resonance spectral analysis. A peculiar property, resembling to Sommelet reaction, of the amino group attached to bridged methylene in bicyclic system is presented. The mass spectra of the amino derivatives of bicyclo [3. 3. 1] nonane system are discussed.
Key concepts: Nonane, Bicyclic molecule, Chemistry, Methylene, Stereochemistry, Medicinal chemistry