Synthesis of alpha-kainic acid from a 7-azabicyclo[2.2.1]heptadiene by tandem radical addition-homoallylic radical rearrangement.
Reductive radical addition of 2-iodoethanol to N-Boc 2-tosyl-7-azabicyclo[2.2.1]heptadiene gives N-Boc syn-7-(2-hydroxyethyl)-4-tosyl-2-azabicyclo[2.2.1]hept-5-ene, which is converted into the neuroexcitants 3-(carboxymethyl)pyrrolidine-2,4-dicarboxylic acid and alpha-kainic acid. [structure: see te...
Main Authors: | Hodgson, D, Hachisu, S, Andrews, MD |
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פורמט: | Journal article |
שפה: | English |
יצא לאור: |
2005
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פריטים דומים
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Stereocontrolled syntheses of kainoid amino acids from 7-azabicyclo[2.2.1]heptadienes using tandem radical addition-homoallylic radical rearrangement.
מאת: Hodgson, D, et al.
יצא לאור: (2005) -
2-Azabicyclo[2.2.1]hept-5-enes from 7-azabicyclo[2.2.1]heptadienes by tandem intermolecular radical addition-homoallylic radical rearrangement
מאת: Hodgson, D, et al.
יצא לאור: (2001) -
2-azabicyclo[2.2.1]-5-heptenes from 7-azabicyclo[2.2.1]heptadienes by tandem intermolecular radical addition - Homoallylic rearrangement.
מאת: Hodgson, D, et al.
יצא לאור: (2001) -
Tandem intermolecular radical addition-rearrangement for azacycle synthesis
מאת: Hodgson, D, et al.
יצא לאור: (2004) -
An epoxide rearrangement-radical rearrangement approach to 6-substituted 2-azabicyclo[2.2.1]-5-heptenes: Synthesis of an epibatidine analogue
מאת: Hodgson, D, et al.
יצא לאור: (1998)