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An epoxide rearrangement - Rad...
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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.
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Detalhes bibliográficos
Main Authors:
Maxwell, C
,
Hodgson, D
,
Matthews, I
Formato:
Journal article
Publicado em:
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
Por
Hodgson, D
,
Maxwell, C
,
Matthews, I
Publicado em 1998
Journal article
Show all versions (2)
Registos relacionados
An epoxide rearrangement-radical rearrangement approach to 6-substituted 2-azabicyclo[2.2.1]-5-heptenes: Synthesis of an epibatidine analogue
Por: Hodgson, D, et al.
Publicado em: (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
Por: Hodgson, D, et al.
Publicado em: (2001)
2-azabicyclo[2.2.1]-5-heptenes from 7-azabicyclo[2.2.1]heptadienes by tandem intermolecular radical addition - Homoallylic rearrangement.
Por: Hodgson, D, et al.
Publicado em: (2001)
2-Azabicyclo[2.2.1]hept-5-enes from 7-azabicyclo[2.2.1]heptadienes by tandem intermolecular radical addition-homoallylic radical rearrangement
Por: Hodgson, D, et al.
Publicado em: (2001)
Synthesis of alpha-kainic acid from a 7-azabicyclo[2.2.1]heptadiene by tandem radical addition-homoallylic radical rearrangement.
Por: Hodgson, D, et al.
Publicado em: (2005)