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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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Bibliografske podrobnosti
Main Authors:
Maxwell, C
,
Hodgson, D
,
Matthews, I
Format:
Journal article
Izdano:
1999
Zaloga
Opis
Other Versions (1)
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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
od
Hodgson, D
,
Maxwell, C
,
Matthews, I
Izdano 1998
Journal article
Show all versions (2)
Podobne knjige/članki
An epoxide rearrangement-radical rearrangement approach to 6-substituted 2-azabicyclo[2.2.1]-5-heptenes: Synthesis of an epibatidine analogue
od: Hodgson, D, et al.
Izdano: (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
od: Hodgson, D, et al.
Izdano: (2001)
2-azabicyclo[2.2.1]-5-heptenes from 7-azabicyclo[2.2.1]heptadienes by tandem intermolecular radical addition - Homoallylic rearrangement.
od: Hodgson, D, et al.
Izdano: (2001)
2-Azabicyclo[2.2.1]hept-5-enes from 7-azabicyclo[2.2.1]heptadienes by tandem intermolecular radical addition-homoallylic radical rearrangement
od: Hodgson, D, et al.
Izdano: (2001)
Synthesis of alpha-kainic acid from a 7-azabicyclo[2.2.1]heptadiene by tandem radical addition-homoallylic radical rearrangement.
od: Hodgson, D, et al.
Izdano: (2005)