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An epoxide rearrangement - Radical rearrangement approach to 6-substituted 2-azabicyclo[2.2.1]-5-heptenes: Synthesis of an epibatidine analogue.

An epoxide rearrangement - Radical rearrangement approach to 6-substituted 2-azabicyclo[2.2.1]-5-heptenes: Synthesis of an epibatidine analogue.

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书目详细资料
Main Authors: Maxwell, C, Hodgson, D, Matthews, I
格式: Journal article
出版: 1999
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  • An epoxide rearrangement-radical rearrangement approach to 6-substituted 2-azabicyclo[2.2.1]-5-heptenes: Synthesis of an epibatidine analogue
    由: Hodgson, D, et al.
    出版: (1998)
  • 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
    由: Hodgson, D, et al.
    出版: (2001)
  • 2-azabicyclo[2.2.1]-5-heptenes from 7-azabicyclo[2.2.1]heptadienes by tandem intermolecular radical addition - Homoallylic rearrangement.
    由: Hodgson, D, et al.
    出版: (2001)
  • 2-Azabicyclo[2.2.1]hept-5-enes from 7-azabicyclo[2.2.1]heptadienes by tandem intermolecular radical addition-homoallylic radical rearrangement
    由: Hodgson, D, et al.
    出版: (2001)
  • Synthesis of alpha-kainic acid from a 7-azabicyclo[2.2.1]heptadiene by tandem radical addition-homoallylic radical rearrangement.
    由: Hodgson, D, et al.
    出版: (2005)

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