Tandem intermolecular radical addition-rearrangement for azacycle synthesis

Tandem intermolecular radical addition-rearrangement for azacycle synthesis

Bibliografski detalji
Glavni autori:	Hodgson, D, Hachisu, S
Format:	Conference item
Izdano:	2004

Slični predmeti

Synthesis of alpha-kainic acid from a 7-azabicyclo[2.2.1]heptadiene by tandem radical addition-homoallylic radical rearrangement.
od: Hodgson, D, i dr.
Izdano: (2005)

Stereocontrolled syntheses of kainoid amino acids from 7-azabicyclo[2.2.1]heptadienes using tandem radical addition-homoallylic radical rearrangement.
od: Hodgson, D, i dr.
Izdano: (2005)

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, i dr.
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, i dr.
Izdano: (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.
od: Hodgson, D, i dr.
Izdano: (2003)

New transformations of azacycles
od: Mortimer, C
Izdano: (2015)

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
od: Bebbington, M, i dr.
Izdano: (2006)

Recent Advances in Synthetic Routes to Azacycles
od: Anh Thu Nguyen, i dr.
Izdano: (2023-03-01)

Synthesis of azabicyclic systems using nitrogen-directed radical rearrangements.
od: Hodgson, D, i dr.
Izdano: (2007)

A one-pot multicomponent reaction for the synthesis of oligoetherols with azacyclic rings
od: Jacek Marek Lubczak, i dr.
Izdano: (2017-12-01)

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
od: Srinivasarao Yaragorla, i dr.
Izdano: (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”
od: Srinivasarao Yaragorla, i dr.
Izdano: (2018-04-01)

Synthesis of mono- and bicyclic azacycles via palladium- and ruthenium-catalysed enynamide cycloisomerisation
od: Walker, P, i dr.
Izdano: (2014)

Palladium-catalyzed cyclization of bromoenynamides to tricyclic azacycles: synthesis of trikentrin-like frameworks.
od: Campbell, C, i dr.
Izdano: (2014)

The tandem radical route to indole alkaloids: an unusual rearrangement reaction
od: Stephen T. Hilton, i dr.
Izdano: (2006-11-01)

Enantioselective access to isoquinuclidines by tropenone desymmetrization and homoallylic radical rearrangement: synthesis of (+)-ibogamine.
od: Hodgson, D, i dr.
Izdano: (2005)

Difunctionalization of Alkenes and Alkynes via Intermolecular Radical and Nucleophilic Additions
od: Hongjun Yao, i dr.
Izdano: (2020-12-01)

An epoxide rearrangement-radical rearrangement approach to 6-substituted 2-azabicyclo[2.2.1]-5-heptenes: Synthesis of an epibatidine analogue
od: Hodgson, D, i dr.
Izdano: (1998)

An epoxide rearrangement - Radical rearrangement approach to 6-substituted 2-azabicyclo[2.2.1]-5-heptenes: Synthesis of an epibatidine analogue.
od: Maxwell, C, i dr.
Izdano: (1999)

Rapid stereoselective syntheses of heteroarene-fused azacycles via diastereoselective conjugate addition of heteroaryl substituted lithium amides
od: Davies, S, i dr.
Izdano: (2018)

A tandem intramolecular Michael-addition/elimination sequence in dihydropyrimidone to quinoline rearrangements
od: Nikola Stiasni, i dr.
Izdano: (2002-08-01)

Tandem catalytic processes involving Rhodium-catalysed intermolecular hydroacylation
od: Lenden, P
Izdano: (2011)

Synthetic studies towards the nor-triterpene pfaffic acid: Synthesis of DEF ring fragment via tandem radical cyclization rearrangement reactions
od: P. J. Biju, i dr.
Izdano: (2004-08-01)

Enantiospecific synthesis of functionalised bicyclo[3.3.1]nonanes from 10-bromocarvones via tandem intermolecular alkylation-intramolecular Michael addition sequence
od: A. Srikrishna, i dr.
Izdano: (2003-02-01)

Tandem intermolecular Suzuki coupling/intramolecular vinyl triflate-arene coupling
od: Willis, M, i dr.
Izdano: (2002)

Tandem intermolecular Suzuki coupling/intramolecular vinyl triflate-arene coupling.
od: Willis, M, i dr.
Izdano: (2002)

Highly enantioenriched 2-azabenzonorbornenes from 7-azabenzonorbornadienes by asymmetric hydroboration-oxidation and tandem deoxygenation-rearrangement-electrophile trapping
od: Hodgson, D, i dr.
Izdano: (2006)

Palladium- and ruthenium-catalyzed cycloisomerization of enynamides and enynhydrazides: a rapid approach to diverse azacyclic frameworks.
od: Walker, P, i dr.
Izdano: (2013)

Epoxide opening-induced tandem 8-azabicyclo[3.2.1]octane to 6-azabicyclo[3.2.1]octane rearrangement-iminium allylation: synthesis of (+/-)-peduncularine.
od: Hodgson, D, i dr.
Izdano: (2010)

2-azabenzonorbornanes from 7-azabenzonorbornanols by a nitrogen-directed neophyl-type radical rearrangement.
od: Hodgson, D, i dr.
Izdano: (2002)

Synthesis of medium-ring lactones via tandem methylenation/Claisen rearrangement of cyclic carbonates
od: Davidson, J, i dr.
Izdano: (2000)

Synthesis of medium-ring lactones via tandem methylenation/Claisen rearrangement of cyclic carbonates
od: Anderson, E, i dr.
Izdano: (2002)

Radical Smiles Rearrangement: An Update
od: Ingrid Allart-Simon, i dr.
Izdano: (2016-07-01)

Ligand bite angle-dependent palladium-catalyzed cyclization of propargylic carbonates to 2-alkynyl azacycles or cyclic dienamides.
od: Daniels, D, i dr.
Izdano: (2014)

An enantioselective epoxide rearrangement - Claisen rearrangement approach to prostaglandins and (+)-iridomyrmecin
od: Hodgson, D, i dr.
Izdano: (1997)

Expedient synthesis of highly substituted pyrroles via tandem rearrangement of α-diazo oxime ethers
od: Jiang, Yaojia, i dr.
Izdano: (2013)

Synthesis of cycloheptanoid natural products via tandem 5-exo cyclization/Claisen rearrangement process
od: Timo V. Ovaska
Izdano: (2010-10-01)

Keep Your TEMPO Up: Nitroxide Radicals as Sensors of Intermolecular Interactions
od: Ilya G. Shenderovich
Izdano: (2024-10-01)

Catalytic asymmetric synthesis of (+)-anthecotulide using enyne and Meyer-Schuster rearrangements.
od: Hodgson, D, i dr.
Izdano: (2011)

Synthesis of the anti-HIV agent (-)-hyperolactone C by using oxonium ylide formation-rearrangement.
od: Hodgson, D, i dr.
Izdano: (2011)