2-Azabicyclo[2.2.1]hept-5-enes from 7-azabicyclo[2.2.1]heptadienes by tandem intermolecular radical addition-homoallylic radical rearrangement

Ítems similars

• 2-azabicyclo[2.2.1]-5-heptenes from 7-azabicyclo[2.2.1]heptadienes by tandem intermolecular radical addition - Homoallylic rearrangement.
  per: Hodgson, D, et al.
  Publicat: (2001)
• Synthesis of alpha-kainic acid from a 7-azabicyclo[2.2.1]heptadiene by tandem radical addition-homoallylic radical rearrangement.
  per: Hodgson, D, et al.
  Publicat: (2005)
• Stereocontrolled syntheses of kainoid amino acids from 7-azabicyclo[2.2.1]heptadienes using tandem radical addition-homoallylic radical rearrangement.
  per: Hodgson, D, et al.
  Publicat: (2005)
• 6-Substituted 2-azabicyclo[2.2.1]hept-5-enes by nitrogen-directed radical rearrangement: Synthesis of an epibatidine analogue with high binding affinity at the nicotinic acetylcholine receptor
  per: Hodgson, D, et al.
  Publicat: (2001)
• Radical deoxygenation of 3-azatricyclo[2.2.1.0(2,6)]heptan-5-ols to 2-azabicyclo[2.2.1]hept-5-enes and 1,2-dihydropyridines
  per: Hodgson, D, et al.
  Publicat: (2009)