Oxidative Dearomatization of 4,5,6,7-Tetrahydro-1H-indoles Obtained by Metal- and Solvent-Free Thermal 5-endo-dig Cyclization: The Route to Erythrina and Lycorine Alkaloids Article

Andreev, Ivan A, Ratmanova, Nina K, Novoselov, Anton M et al. (2016). Oxidative Dearomatization of 4,5,6,7-Tetrahydro-1H-indoles Obtained by Metal- and Solvent-Free Thermal 5-endo-dig Cyclization: The Route to Erythrina and Lycorine Alkaloids . CHEMISTRY-A EUROPEAN JOURNAL, 22(21), 7262-7267. 10.1002/chem.201600273

cited authors

  • Andreev, Ivan A; Ratmanova, Nina K; Novoselov, Anton M; Belov, Dmitry S; Seregina, Irina F; Kurkin, Alexander V

sustainable development goals

authors

publication date

  • May 17, 2016

webpage

published in

keywords

  • (+/-)-3-DEMETHOXYERYTHRATIDINONE
  • 4,5,6,7-tetrahydroindoles
  • Chemistry
  • Chemistry, Multidisciplinary
  • ENAMINO-KETONES
  • FACILE SYNTHESIS
  • FORMAL TOTAL-SYNTHESIS
  • GAMMA-LACTAMS
  • HEXAHYDROAPOERYSOPINE
  • ONE-POT SYNTHESIS
  • Physical Sciences
  • RADICAL CYCLIZATIONS
  • SIMPLE FURANS
  • Science & Technology
  • WATER
  • alkaloids
  • green chemistry
  • thermally induced cyclization
  • total synthesis

Digital Object Identifier (DOI)

publisher

  • WILEY-V C H VERLAG GMBH

start page

  • 7262

end page

  • 7267

volume

  • 22

issue

  • 21