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Chem Pharm Bull (Tokyo) ; 60(8): 1063-6, 2012.
Article in English | MEDLINE | ID: mdl-22863711

ABSTRACT

The preparation of novel tetrahydro-1H-pyrazolo[4,3-c]pyridines is reported. Pivotal to the synthesis of these compounds was the development of mild reaction conditions to generate a highly functionalized nitrilimine capable of undergoing an intramolecular cycloaddition with a tethered alkyne. The desired cycloadduct was formed as an equal mixture of diastereomers.


Subject(s)
Cyclization , Imines/chemistry , Nitriles/chemistry , Pyridines/chemical synthesis , Magnetic Resonance Spectroscopy , Mass Spectrometry , Models, Molecular
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