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Synthesis of N-phenacyl Pyridines and N-phenacyl Piperidines

These N-substituted piperidines, because of their similarity in structure to the pressor amines, are expected to be physiologically active. By varying the position and size of the alkyl groups attached to the pyridine ring, difference in degree and type of physiological activity are likely.

Identiferoai:union.ndltd.org:unt.edu/info:ark/67531/metadc798281
Date06 1900
CreatorsGoode, William E.
PublisherNorth Texas State Teachers College
Source SetsUniversity of North Texas
LanguageEnglish
Detected LanguageEnglish
TypeThesis or Dissertation
FormatText
RightsPublic, Copyright, Copyright is held by the author, unless otherwise noted. All rights

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