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A New and Efficient Approach to the Synthesis of Nicotine and Anabasine Analogues.


ABSTRACT: A straightforward and practical approach was established for the synthesis of nicotine and anabasine analogues by the cyclization of mesylated 1-(3-pyridinyl)-1,4, and 1,5-diol derivatives to form the pyrrolidino or piperidino fragments. Nicotine analogue (S)-15 was prepared with good enantioselectivity using the developed azacyclization procedure of nonracemic (R)-1-pyridin-3-yl-butane-1,4-diol, which was obtained by the borane-mediated reduction of ketone 12 in the presence of the spiroborate ester derived from diphenyl prolinol and ethylene glycol.

SUBMITTER: Huang K 

PROVIDER: S-EPMC2811585 | biostudies-literature | 2009 Nov

REPOSITORIES: biostudies-literature

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A New and Efficient Approach to the Synthesis of Nicotine and Anabasine Analogues.

Huang Kun K   Ortiz-Marciales Margarita M   De Jesús Melvin M   Stepanenko Viatcheslav V  

Journal of heterocyclic chemistry 20091101 6


A straightforward and practical approach was established for the synthesis of nicotine and anabasine analogues by the cyclization of mesylated 1-(3-pyridinyl)-1,4, and 1,5-diol derivatives to form the pyrrolidino or piperidino fragments. Nicotine analogue (S)-15 was prepared with good enantioselectivity using the developed azacyclization procedure of nonracemic (R)-1-pyridin-3-yl-butane-1,4-diol, which was obtained by the borane-mediated reduction of ketone 12 in the presence of the spiroborate  ...[more]

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