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8-phenyl-10,10a-dihydropyrido

Marx1, Eberbach

  • 1Institut fur Organische Chemie und Biochemie der Universitat Freiburg, Germany.

Chemistry (Weinheim an Der Bergstrasse, Germany)
|July 14, 2000
PubMed
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Treatment of pyridinium bromides yields dihydropyridoazepines via ylide intermediates. Quantum mechanical calculations explain the observed 8pi-electrocyclization selectivity in this heterocyclic synthesis.

Area of Science:

  • Organic Chemistry
  • Heterocyclic Chemistry
  • Computational Chemistry

Background:

  • Pyridinium salts are versatile precursors in organic synthesis.
  • Electrocyclization reactions are key transformations in forming cyclic systems.
  • Understanding reaction mechanisms and selectivity is crucial for synthetic strategy.

Purpose of the Study:

  • To investigate the reaction of pyridinium bromides with base.
  • To elucidate the mechanism and stereoselectivity of the observed cyclization.
  • To provide a theoretical basis for the reaction's outcome using computational methods.

Main Methods:

  • Base-induced reaction of pyridinium bromides (11a-e).
  • Isolation and characterization of monomolecular products (14a-e).

Related Experiment Videos

  • Quantum mechanical calculations to analyze the electrocyclization pathway.

    • Main Results:

    • Formation of dihydropyridoazepines (14a-e) as the sole monomolecular products.
    • Identification of ylide intermediates (12) preceding cyclization.
    • Experimental evidence confirmed 8pi-electrocyclization, with no 6pi-cyclization products detected.

    Conclusions:

    • The base treatment of pyridinium bromides selectively yields dihydropyridoazepines through an 8pi-electrocyclization pathway.
    • Quantum mechanical calculations successfully rationalize the observed periselective electrocyclization.
    • The study clarifies the reaction mechanism, highlighting the importance of ylide intermediates in forming seven-membered heterocyclic rings.