Tandem intermolecular radical addition-rearrangement for azacycle synthesis
Váldodahkkit: | Hodgson, D, Hachisu, S |
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Materiálatiipa: | Conference item |
Almmustuhtton: |
2004
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Geahča maid
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Synthesis of alpha-kainic acid from a 7-azabicyclo[2.2.1]heptadiene by tandem radical addition-homoallylic radical rearrangement.
Dahkki: Hodgson, D, et al.
Almmustuhtton: (2005) -
Stereocontrolled syntheses of kainoid amino acids from 7-azabicyclo[2.2.1]heptadienes using tandem radical addition-homoallylic radical rearrangement.
Dahkki: Hodgson, D, et al.
Almmustuhtton: (2005) -
2-Azabicyclo[2.2.1]hept-5-enes from 7-azabicyclo[2.2.1]heptadienes by tandem intermolecular radical addition-homoallylic radical rearrangement
Dahkki: Hodgson, D, et al.
Almmustuhtton: (2001) -
2-azabicyclo[2.2.1]-5-heptenes from 7-azabicyclo[2.2.1]heptadienes by tandem intermolecular radical addition - Homoallylic rearrangement.
Dahkki: Hodgson, D, et al.
Almmustuhtton: (2001) -
Development of two processes for the synthesis of bridged azabicyclic systems: intermolecular radical addition-homoallylic rearrangements leading to 2-azanorborn-5-enes and neophyl-type radical rearrangements to 2-azabenzonorbornanes.
Dahkki: Hodgson, D, et al.
Almmustuhtton: (2003)