Highly efficient thermal cyclization reactions of alkylidene esters in continuous flow to give aromatic/heteroaromatic derivatives Article

Lengyel, Laszlo, Nagy, Tibor Zs, Sipos, Gellert et al. (2012). Highly efficient thermal cyclization reactions of alkylidene esters in continuous flow to give aromatic/heteroaromatic derivatives . TETRAHEDRON LETTERS, 53(7), 738-743. 10.1016/j.tetlet.2011.11.125

cited authors

  • Lengyel, Laszlo; Nagy, Tibor Zs; Sipos, Gellert; Jones, Richard; Dorman, Gyoergy; Uerge, Laszlo; Darvas, Ferenc

authors

publication date

  • February 15, 2012

webpage

published in

keywords

  • 4-AMINOQUINOLINES
  • Benzannulation
  • Biphenyls
  • CYCLOADDITION REACTIONS
  • Chemistry
  • Chemistry, Organic
  • Conrad Limpach reaction
  • Flow chemistry
  • Gould Jacobs reaction
  • MELDRUMS
  • Microreactor
  • PYROLYSIS
  • Physical Sciences
  • Pyridopyrimidinones
  • Quinolines
  • Science & Technology
  • Thermal cyclization

Digital Object Identifier (DOI)

publisher

  • PERGAMON-ELSEVIER SCIENCE LTD

start page

  • 738

end page

  • 743

volume

  • 53

issue

  • 7