1977Journal of Heterocyclic ChemistryRequires access

Synthesis and conformational analysis of isomeric 3‐propananilidotropanes

Jerome R. Bagley, Thomas N. Riley

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Abstract

Abstract The isomeric 3‐anilino and 3‐propananilidotropanes have been synthesized and obtained in isomerically pure form. The configurations and solute conformations of these isomers were studied via glc and nrar analysis. The 3β‐isomers have been shown to exist in the normal piper‐idine chair conformation whereas the 3α‐anilino tropane exists in a flattened piperidine chair conformation and the 3α‐propananilidotropane isomer preferentially exists in a conformation in which the piperidine ring system is a boat.

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Abstract The isomeric 3‐anilino and 3‐propananilidotropanes have been synthesized and obtained in isomerically pure form. The configurations and solute conformations of these isomers were studied via glc and nrar analysis. The 3β‐isomers have been shown to exist in the normal piper‐idine chair conformation whereas the 3α‐anilino tropane exists in a flattened piperidine chair conformation and the 3α‐propananilidotropane isomer preferentially exists in a conformation in which the piperidine ring system is a boat.

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Available abstract

Abstract The isomeric 3‐anilino and 3‐propananilidotropanes have been synthesized and obtained in isomerically pure form. The configurations and solute conformations of these isomers were studied via glc and nrar analysis. The 3β‐isomers have been shown to exist in the normal piper‐idine chair conformation whereas the 3α‐anilino tropane exists in a flattened piperidine chair conformation and the 3α‐propananilidotropane isomer preferentially exists in a conformation in which the piperidine ring system is a boat.

Key concepts: Chemistry, Piperidine, Tropane, Cyclohexane conformation, Ring (chemistry), Stereochemistry, Molecule, Organic chemistry

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