Tandem intermolecular radical addition-rearrangement for azacycle synthesis

Tandem intermolecular radical addition-rearrangement for azacycle synthesis

Bibliografiska uppgifter
Huvudupphovsmän:	Hodgson, D, Hachisu, S
Materialtyp:	Conference item
Publicerad:	2004

Liknande verk

Synthesis of alpha-kainic acid from a 7-azabicyclo[2.2.1]heptadiene by tandem radical addition-homoallylic radical rearrangement.
av: Hodgson, D, et al.
Publicerad: (2005)

Stereocontrolled syntheses of kainoid amino acids from 7-azabicyclo[2.2.1]heptadienes using tandem radical addition-homoallylic radical rearrangement.
av: Hodgson, D, et al.
Publicerad: (2005)

2-Azabicyclo[2.2.1]hept-5-enes from 7-azabicyclo[2.2.1]heptadienes by tandem intermolecular radical addition-homoallylic radical rearrangement
av: Hodgson, D, et al.
Publicerad: (2001)

2-azabicyclo[2.2.1]-5-heptenes from 7-azabicyclo[2.2.1]heptadienes by tandem intermolecular radical addition - Homoallylic rearrangement.
av: Hodgson, D, et al.
Publicerad: (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.
av: Hodgson, D, et al.
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New transformations of azacycles
av: Mortimer, C
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A) Nitrogen-directed homoallylic free-radical rearrangements for the construction of bridged azacycles B) Studies on a total synthesis of the microbial immunosuppressive agent FR901483 C) Phosphinoboranes as bifunctional organocatalysts and ambiphilic ligands
av: Bebbington, M, et al.
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Recent Advances in Synthetic Routes to Azacycles
av: Anh Thu Nguyen, et al.
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Synthesis of azabicyclic systems using nitrogen-directed radical rearrangements.
av: Hodgson, D, et al.
Publicerad: (2007)

A one-pot multicomponent reaction for the synthesis of oligoetherols with azacyclic rings
av: Jacek Marek Lubczak, et al.
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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
av: Srinivasarao Yaragorla, et al.
Publicerad: (2018-03-01)

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”
av: Srinivasarao Yaragorla, et al.
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Synthesis of mono- and bicyclic azacycles via palladium- and ruthenium-catalysed enynamide cycloisomerisation
av: Walker, P, et al.
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Palladium-catalyzed cyclization of bromoenynamides to tricyclic azacycles: synthesis of trikentrin-like frameworks.
av: Campbell, C, et al.
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The tandem radical route to indole alkaloids: an unusual rearrangement reaction
av: Stephen T. Hilton, et al.
Publicerad: (2006-11-01)

Enantioselective access to isoquinuclidines by tropenone desymmetrization and homoallylic radical rearrangement: synthesis of (+)-ibogamine.
av: Hodgson, D, et al.
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Difunctionalization of Alkenes and Alkynes via Intermolecular Radical and Nucleophilic Additions
av: Hongjun Yao, et al.
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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
av: Hodgson, D, et al.
Publicerad: (1998)

An epoxide rearrangement - Radical rearrangement approach to 6-substituted 2-azabicyclo[2.2.1]-5-heptenes: Synthesis of an epibatidine analogue.
av: Maxwell, C, et al.
Publicerad: (1999)

Rapid stereoselective syntheses of heteroarene-fused azacycles via diastereoselective conjugate addition of heteroaryl substituted lithium amides
av: Davies, S, et al.
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A tandem intramolecular Michael-addition/elimination sequence in dihydropyrimidone to quinoline rearrangements
av: Nikola Stiasni, et al.
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Tandem catalytic processes involving Rhodium-catalysed intermolecular hydroacylation
av: Lenden, P
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Synthetic studies towards the nor-triterpene pfaffic acid: Synthesis of DEF ring fragment via tandem radical cyclization rearrangement reactions
av: P. J. Biju, et al.
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Enantiospecific synthesis of functionalised bicyclo[3.3.1]nonanes from 10-bromocarvones via tandem intermolecular alkylation-intramolecular Michael addition sequence
av: A. Srikrishna, et al.
Publicerad: (2003-02-01)

Tandem intermolecular Suzuki coupling/intramolecular vinyl triflate-arene coupling
av: Willis, M, et al.
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Tandem intermolecular Suzuki coupling/intramolecular vinyl triflate-arene coupling.
av: Willis, M, et al.
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Highly enantioenriched 2-azabenzonorbornenes from 7-azabenzonorbornadienes by asymmetric hydroboration-oxidation and tandem deoxygenation-rearrangement-electrophile trapping
av: Hodgson, D, et al.
Publicerad: (2006)

Palladium- and ruthenium-catalyzed cycloisomerization of enynamides and enynhydrazides: a rapid approach to diverse azacyclic frameworks.
av: Walker, P, et al.
Publicerad: (2013)

Epoxide opening-induced tandem 8-azabicyclo[3.2.1]octane to 6-azabicyclo[3.2.1]octane rearrangement-iminium allylation: synthesis of (+/-)-peduncularine.
av: Hodgson, D, et al.
Publicerad: (2010)

2-azabenzonorbornanes from 7-azabenzonorbornanols by a nitrogen-directed neophyl-type radical rearrangement.
av: Hodgson, D, et al.
Publicerad: (2002)

Synthesis of medium-ring lactones via tandem methylenation/Claisen rearrangement of cyclic carbonates
av: Davidson, J, et al.
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Synthesis of medium-ring lactones via tandem methylenation/Claisen rearrangement of cyclic carbonates
av: Anderson, E, et al.
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Radical Smiles Rearrangement: An Update
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Ligand bite angle-dependent palladium-catalyzed cyclization of propargylic carbonates to 2-alkynyl azacycles or cyclic dienamides.
av: Daniels, D, et al.
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An enantioselective epoxide rearrangement - Claisen rearrangement approach to prostaglandins and (+)-iridomyrmecin
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Expedient synthesis of highly substituted pyrroles via tandem rearrangement of α-diazo oxime ethers
av: Jiang, Yaojia, et al.
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Synthesis of cycloheptanoid natural products via tandem 5-exo cyclization/Claisen rearrangement process
av: Timo V. Ovaska
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Keep Your TEMPO Up: Nitroxide Radicals as Sensors of Intermolecular Interactions
av: Ilya G. Shenderovich
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Catalytic asymmetric synthesis of (+)-anthecotulide using enyne and Meyer-Schuster rearrangements.
av: Hodgson, D, et al.
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Synthesis of the anti-HIV agent (-)-hyperolactone C by using oxonium ylide formation-rearrangement.
av: Hodgson, D, et al.
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