Tandem intermolecular radical addition-rearrangement for azacycle synthesis

Tandem intermolecular radical addition-rearrangement for azacycle synthesis

Podrobná bibliografie
Hlavní autoři:	Hodgson, D, Hachisu, S
Médium:	Conference item
Vydáno:	2004

Podobné jednotky

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Stereocontrolled syntheses of kainoid amino acids from 7-azabicyclo[2.2.1]heptadienes using tandem radical addition-homoallylic radical rearrangement.
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Correction to “Highly Regioselective Synthesis of Oxindolyl-Pyrroles and Quinolines via a One-Pot, Sequential Meyer–Schuster Rearrangement, Anti-Michael Addition/C(sp3)–H Functionalization, and Azacyclization”
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Highly enantioenriched 2-azabenzonorbornenes from 7-azabenzonorbornadienes by asymmetric hydroboration-oxidation and tandem deoxygenation-rearrangement-electrophile trapping
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Epoxide opening-induced tandem 8-azabicyclo[3.2.1]octane to 6-azabicyclo[3.2.1]octane rearrangement-iminium allylation: synthesis of (+/-)-peduncularine.
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