2-Azabicyclo[2.2.1]hept-5-enes from 7-azabicyclo[2.2.1]heptadienes by tandem intermolecular radical addition-homoallylic radical rearrangement

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Hodgson, D, Bebbington, M, Willis, P
التنسيق:	Journal article
اللغة:	English
منشور في:	2001

2-azabicyclo[2.2.1]-5-heptenes from 7-azabicyclo[2.2.1]heptadienes by tandem intermolecular radical addition - Homoallylic rearrangement.
حسب: Hodgson, D, وآخرون
منشور في: (2001)

Synthesis of alpha-kainic acid from a 7-azabicyclo[2.2.1]heptadiene by tandem radical addition-homoallylic radical rearrangement.
حسب: Hodgson, D, وآخرون
منشور في: (2005)

Stereocontrolled syntheses of kainoid amino acids from 7-azabicyclo[2.2.1]heptadienes using tandem radical addition-homoallylic radical rearrangement.
حسب: Hodgson, D, وآخرون
منشور في: (2005)

6-Substituted 2-azabicyclo[2.2.1]hept-5-enes by nitrogen-directed radical rearrangement: Synthesis of an epibatidine analogue with high binding affinity at the nicotinic acetylcholine receptor
حسب: Hodgson, D, وآخرون
منشور في: (2001)

Radical deoxygenation of 3-azatricyclo[2.2.1.0(2,6)]heptan-5-ols to 2-azabicyclo[2.2.1]hept-5-enes and 1,2-dihydropyridines
حسب: Hodgson, D, وآخرون
منشور في: (2009)

An epoxide rearrangement-radical rearrangement approach to 6-substituted 2-azabicyclo[2.2.1]-5-heptenes: Synthesis of an epibatidine analogue
حسب: Hodgson, D, وآخرون
منشور في: (1998)

An epoxide rearrangement - Radical rearrangement approach to 6-substituted 2-azabicyclo[2.2.1]-5-heptenes: Synthesis of an epibatidine analogue.
حسب: Maxwell, C, وآخرون
منشور في: (1999)

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.
حسب: Hodgson, D, وآخرون
منشور في: (2003)

Synthesis of new 7-azabicyclo[2.2.1]heptane derivatives
حسب: José Marco-Contelles, وآخرون
منشور في: (2009-04-01)

Stereoselective Ring-Opening Metathesis Polymerization (ROMP) of Methyl-N-(1-phenylethyl)-2-azabicyclo[2.2.1]hept-5-ene-3-carboxylate by Molybdenum and Tungsten Initiators
حسب: Jeong, Hyangsoo, وآخرون
منشور في: (2017)

Reductive transformation of a hydroxyiodoketone of 8-azabicyclo [3.2.1] octane into 7-azabicyclo [2.2.1] heptane with lithium aluminium hydrile /
حسب: 431255 Sarel, Shalom, وآخرون

tert-Butyl 3-oxo-2-oxa-5-azabicyclo[2.2.1]heptane-5-carboxylate
حسب: Claude Didierjean, وآخرون
منشور في: (2008-10-01)

N-Carbamothioylamino-7-oxabicyclo[2.2.1]hept-5-ene-2,3-dicarboximide
حسب: Jian Li
منشور في: (2010-12-01)

One-step transformation of 2-oxa-3-azabicyclo[2.2.1]heptene and 2-carbomethoxy–2,3-diazabicyclo[2.2.1]heptane to ion uptake systems
حسب: Subramania Ranganathan, وآخرون
منشور في: (2004-05-01)

Crystal structure of benzyl 3-oxo-2-oxa-5-azabicyclo[2.2.1]heptane-5-carboxylate
حسب: Suvratha Krishnamurthy, وآخرون
منشور في: (2015-07-01)

Swern Oxidation of Bicyclo[2.2.1]hept-5-ene-2,3-diol and Its Pyrazine-fused Derivatives: An Improved Synthesis of Bicyclo[2.2.1]hept-5-ene-2,3-dione and An Unexpected Ring-Opening Reaction
حسب: Sayuri Kobayashi, وآخرون
منشور في: (2000-09-01)

Epoxide opening-induced tandem 8-azabicyclo[3.2.1]octane to 6-azabicyclo[3.2.1]octane rearrangement-iminium allylation: synthesis of (+/-)-peduncularine.
حسب: Hodgson, D, وآخرون
منشور في: (2010)

Hydroxylation of 1-azabicyclo[4.1.0]hept-3-enes formed by Diels–Alder reactions of benzyl 2H-azirine-3-carboxylate
حسب: Jamie F. Bickley, وآخرون
منشور في: (2002-09-01)

Design, Synthesis and Biological Evaluation of Neogliptin, a Novel 2-Azabicyclo[2.2.1]heptane-Based Inhibitor of Dipeptidyl Peptidase-4 (DPP-4)
حسب: Ivan O. Maslov, وآخرون
منشور في: (2022-02-01)

Acid-catalyzed ring-opening reactions of a cyclopropanated 3-aza-2-oxabicyclo[2.2.1]hept-5-ene with alcohols
حسب: Katrina Tait, وآخرون
منشور في: (2017-12-01)

Diisoamyl (1R, 4S)-7-oxabicyclo[2.2.1]hept-5-ene-2,3-dicarboxylate
حسب: Brandon Quillian, وآخرون
منشور في: (2024-07-01)

2-Propyl-N′-[1,7,7-trimethylbicyclo[2.2.1]hept-2-ylidene]pentanehydrazide
حسب: Mariia Nesterkina, وآخرون
منشور في: (2020-10-01)

2-(Bicyclo[2.2.1]hept-5-en-2-yl)-1H-pyrrolo[2,3-b]pyridine
حسب: Roland Selig, وآخرون
منشور في: (2010-07-01)

Stereochemistry of ring-opening/cross metathesis reactions of exo- and endo-7-oxabicyclo[2.2.1]hept-5-ene-2-carbonitriles with allyl alcohol and allyl acetate
حسب: Piotr Wałejko, وآخرون
منشور في: (2015-10-01)

Enantioselective rearrangements of bicyclo[2.2.1]- and bicyclo[2.2.2]alkene-derived achiral epoxides to ketones
حسب: Hodgson, D, وآخرون
منشور في: (1997)

One-Step Introduction of Two Substituents onto 7-Oxabicyclo[2.2.1]hept-5-en-2-one Derivatives via Radical Phenylselanyl-Group Transfer Reactions
حسب: Philippe Renaud, وآخرون
منشور في: (1994-10-01)

7-Benzenesulfonamido-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]octa-2-ene-2-carboxylic acid monohydrate
حسب: Shahzad Sharif, وآخرون
منشور في: (2010-01-01)

Crystal structure of di(1R,45)-1,7,7’-trimethyl-3-bromobicyclo[2.2.1]hept-2-ene carboxylate, (С10H14Вг)2СО3
حسب: Peters K., وآخرون
منشور في: (2000-01-01)

Base-induced rearrangements of bicyclo[2.2.1] and bicyclo[2.2.2]alkene-derived epoxides to ketones and alcohols
حسب: Hodgson, D, وآخرون
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Enantioselective access to isoquinuclidines by tropenone desymmetrization and homoallylic radical rearrangement: synthesis of (+)-ibogamine.
حسب: Hodgson, D, وآخرون
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endo-N-(5,5-Dimethyl-6-methylene-bicyclo[2.2.1]hept-2-yl)-4-methyl-benzenesulfonamide
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منشور في: (2004-03-01)

2-(2-Azabicyclo[3.2.1]octa-3,6-dien-2-yl)-1,3-dimethoxyimidazolium hexafluoridophosphate
حسب: Simone Haslinger, وآخرون
منشور في: (2016-09-01)

Crystal structure of 5-chloro-7-(diphenylmethylene)-5,6-(exo,endo)- bis(phenylsulfonyl)-bicyclo[2.2.1]hept-2 -ene, C32H25O4S2CI
حسب: Peters Κ., وآخرون
منشور في: (1997-12-01)

Crystal structure of 5-chloro-7-(diphenylmethylene)-5,6-(endo,endo)- bis(phenylsulfonyl)-bicyclo[2.2.1]hept-2-ene, C32H25O4S2CI
حسب: Peters Κ., وآخرون
منشور في: (1997-12-01)

Crystal structure of 5-chloro-7-(diphenylmethylene)-5,6-(exo,endo)- bis(phenylsulfonyl)-bicyclo[2.2.1]hept-2 -ene, C32H25O4S2CI
حسب: Peters Κ., وآخرون
منشور في: (1997-12-01)

Crystal structure of 5-chloro-7-(diphenylmethylene)-5,6-(endo,endo)- bis(phenylsulfonyl)-bicyclo[2.2.1]hept-2-ene, C32H25O4S2CI
حسب: Peters Κ., وآخرون
منشور في: (1997-12-01)

2-azabenzonorbornanes from 7-azabenzonorbornanols by a nitrogen-directed neophyl-type radical rearrangement.
حسب: Hodgson, D, وآخرون
منشور في: (2002)

Crystal structure of diaquabis(bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylate-κ4O, O′:/O′′,O′′′)bis-(2,2′-bipyridine-κ2N, N′)dicadmium(II) hydrate
حسب: Hai-Xia Wu, وآخرون
منشور في: (2016-03-01)

New mixed-ligand Ni(II) and Zn(II) macrocyclic complexes with bridged (endo,endo)-bicyclo [2.2.1]hept-5-ene-2,3-dicarboxylate: Synthesis, characterization, antimicrobial and cytotoxic activity
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منشور في: (2019-01-01)

Multigram Synthesis of 2-Azabicyclo[2.1.1]hexane-1-Carboxylates (2,4-Methanoprolines) – Promising Bicyclic Proline Analogs
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منشور في: (2024-12-01)

2-Azabicyclo[2.2.1]hept-5-enes from 7-azabicyclo[2.2.1]heptadienes by tandem intermolecular radical addition-homoallylic radical rearrangement

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