771-98-2 | 1-Phenyl-1-cyclohexene

[1]OrganicLetters,2009,vol.11,#22,p.5286-5289

[1]Tetrahedron,1990,vol.46,#18,p.6331-6342

[1]JournaloftheAmericanChemicalSociety,1948,vol.70,p.3352,3354

[1]JournalofOrganicChemistry,1991,vol.56,p.95-102

[2]JournalofOrganicChemistry,2014,vol.79,p.4270-4276

[3]JournalofOrganicChemistry,1999,vol.64,p.2966-2968

[4]CanadianJournalofChemistry,1985,vol.63,p.3186-3194

[5]Tetrahedron,1998,vol.54,p.7457-7464

[6]SyntheticCommunications,2013,vol.43,p.2256-2264

[7]JournaloftheAmericanChemicalSociety,2002,vol.124,p.11946-11954

[8]Organometallics,2011,vol.30,p.379-382

[9]JournalofPorphyrinsandPhthalocyanines,2012,vol.16,p.1032-1039

[10]JournalofOrganicChemistry,1998,vol.63,p.2810-2811

[11]Tetrahedron,1999,vol.55,p.2341-2352

[12]JournaloftheAmericanChemicalSociety,2001,vol.123,p.2933-2934

[13]ChemSusChem,2015,vol.8,p.4056-4063

[14]OrganicLetters,2018,vol.20,p.2015-2019

[15]Patent:JP2018/70482,2018,A.Locationinpatent:Paragraph0095;0096;0097;0099

[16]JournaloftheAmericanChemicalSociety,1997,vol.119,p.6189-6190

[17]Patent:US2006/161011,2006,A1.Locationinpatent:Page/Pagecolumn5

[18]JournalofOrganicChemistry,1997,vol.62,p.8964-8965

[19]JournalofOrganicChemistry,1997,vol.62,p.8964-8965

[20]Tetrahedron,2006,vol.62,p.6650-6658

[21]AdvancedSynthesisandCatalysis,2009,vol.351,p.348-352

[22]TetrahedronLetters,1999,vol.40,p.8029-8032

[23]Patent:CN111217769,2020,A.Locationinpatent:Paragraph0038-0079

[24]TetrahedronLetters,1999,vol.40,p.3991-3994

[25]JournalofOrganicChemistry,1998,vol.63,p.9888-9894

[26]JournalofOrganicChemistry,2000,vol.65,p.8807-8810

[27]JournalofOrganicChemistry,1998,vol.63,p.6425-6426

[28]JournalofOrganicChemistry,2005,vol.70,p.9610-9613

[29]AngewandteChemie-InternationalEdition,2006,vol.45,p.5502-5505

[30]TetrahedronAsymmetry,2005,vol.16,p.3536-3561

[31]OrganicLetters,2005,vol.7,p.5015-5018

[32]TetrahedronLetters,2007,vol.48,p.2691-2695

[33]JournalofOrganicChemistry,1998,vol.63,p.2774-2777

[34]Synthesis,2005,p.3405-3411

[35]JournaloftheChemicalSociety,DaltonTransactions,1998,p.3559-3564

[36]JournaloftheAmericanChemicalSociety,2000,vol.122,p.4039-4043

[37]ChemSusChem,2011,vol.4,p.1813-1822

[38]Tetrahedron,2013,vol.69,p.10009-10013

[39]TetrahedronLetters,2006,vol.47,p.1923-1926

[40]ChemicalandPharmaceuticalBulletin,2011,vol.59,p.799-801

[41]Tetrahedron,2005,vol.61,p.12053-12057

[42]JournaloftheAmericanChemicalSociety,2013,vol.135,p.6177-6183

[43]JournaloftheAmericanChemicalSociety,2013,vol.135,p.10036-10039

[44]RSCAdvances,2016,vol.6,p.79085-79089

[45]Synlett,2017,vol.28,p.235-238

[46]ZhurnalRusskagoFiziko-KhimicheskagoObshchestva,1924,vol.55,p.66    ChemischesZentralblatt,1925,vol.96,p.222

[47]RecueildesTravauxChimiquesdesPays-Bas,1928,vol.47,p.691

[48]Tetrahedron,1994,vol.50,p.3663-3672

[49]TetrahedronAsymmetry,1997,vol.8,p.3481-3487

[50]JournalofOrganicChemistry,1999,vol.64,p.6227-6234

[51]JournalofOrganicChemistry,1999,vol.64,p.7267-7270

[52]JournalofOrganicChemistry,2003,vol.68,p.3232-3237

[53]AdvancedSynthesisandCatalysis,2005,vol.347,p.45-49

[54]OrganicLetters,2005,vol.7,p.987-990

[55]BioorganicandMedicinalChemistryLetters,2006,vol.16,p.354-357

[56]EuropeanJournalofOrganicChemistry,2006,p.803-813

[57]JournalofOrganometallicChemistry,2006,vol.691,p.4419-4433

[58]ChemicalCommunications,2000,p.1165-1166

[59]JournalofOrganicChemistry,2001,vol.66,p.6926-6931

[60]ChemicalCommunications,2003,p.1058-1059

[61]ChemicalCommunications,2000,p.2415-2416

[62]OrganicandBiomolecularChemistry,2007,vol.5,p.2109-2113

[63]Tetrahedron,2008,vol.64,p.9253-9257

[64]AdvancedSynthesisandCatalysis,2008,vol.350,p.802-806

[65]EuropeanJournalofOrganicChemistry,2008,p.5387-5390

[66]OrganicLetters,2008,vol.10,p.2291-2294

[67]AdvancedSynthesisandCatalysis,2008,vol.350,p.1867-1874

[68]JournalofMolecularCatalysisA:Chemical,2010,vol.328,p.60-67

[69]InorganicChemistry,2011,vol.50,p.1775-1785

[70]GreenChemistry,2011,vol.13,p.1230-1237

[71]CatalysisCommunications,2011,vol.12,p.923-926

[72]CatalysisCommunications,2011,vol.15,p.52-55

[73]CurrentMedicinalChemistry,2012,vol.19,p.763-769

[74]DaltonTransactions,2013,vol.42,p.3721-3734

[75]RSCAdvances,2014,vol.4,p.1601-1608

[76]JournalofSulfurChemistry,2013,vol.34,p.671-676

[77]NewJournalofChemistry,2014,vol.38,p.2917-2926

[78]Catalysisscienceandtechnology,2013,vol.3,p.2330-2339

[79]InorganicChemistry,2015,vol.54,p.4998-5012

[80]NewJournalofChemistry,2015,vol.39,p.9879-9885

[81]JournalofMolecularCatalysisA:Chemical,2015,vol.398,p.376-390

[82]CatalysisCommunications,2016,vol.83,p.78-81

[83]AustralianJournalofChemistry,2016,vol.69,p.817-825

[84]InorganicChemistry,2016,vol.55,p.8160-8173

[85]CatalysisCommunications,2017,vol.95,p.88-91

[86]EuropeanJournalofOrganicChemistry,2017,vol.2017,p.1502-1509

[87]AustralianJournalofChemistry,2017,vol.70,p.1039-1047

[88]GreenChemistry,2015,vol.17,p.442-452

[89]RSCAdvances,2018,vol.8,p.37303-37306

[90]EuropeanJournalofOrganicChemistry,2019,vol.2019,p.2401-2408

[91]JournalofOrganicChemistry,2019,vol.84,p.6813-6829

[92]Patent:CN110950822,2020,A.Locationinpatent:Paragraph0037-0038

[1]TetrahedronLetters,2004,vol.45,p.6159-6163

[2]ChineseChemicalLetters,2015,vol.26,p.248-250

[3]AngewandteChemie-InternationalEdition,2012,vol.51,p.5730-5734

[4]RecueildesTravauxChimiquesdesPays-Bas,1948,vol.67,p.489,506

[5]JournaloftheAmericanChemicalSociety,1959,vol.81,p.658,661

[6]SyntheticCommunications,1990,vol.20,p.3265-3271

[7]Tetrahedron,1986,vol.42,p.5511-5514

[8]JournalofChemicalResearch-PartS,1997,p.64-65

[9]BulletinoftheChemicalSocietyofJapan,1982,vol.55,p.3941-3942

[10]BulletindelaSocieteChimiquedeFrance,1915,vol.<4>17,p.101

[11]Tetrahedron,2012,vol.68,p.4320-4327

[12]JournaloftheAmericanChemicalSociety,2013,vol.135,p.6177-6183

[1]AdvancedSynthesisandCatalysis,2005,vol.347,p.1889-1892

[2]Patent:EP1726577,2006,A1.Locationinpatent:Page/Pagecolumn8-9;13

[3]Chemistry-AEuropeanJournal,2018,vol.24,p.3403-3407

[4]CatalysisToday,2020,vol.346,p.69-75

[5]ACSCatalysis,2018,vol.8,p.342-348

[6]Labonachip,2011,vol.11,p.378-380

[7]TetrahedronLetters,2009,vol.50,p.1817-1819

[8]ACSCatalysis,2019,vol.9,p.7596-7606

[9]Synthesis,1993,p.693-699

[10]Polyhedron,2016,vol.120,p.36-43

[11]GreenChemistry,2015,vol.17,p.1408-1413

[12]ComptesRendusHebdomadairesdesSeancesdel'AcademiedesSciences,1912,vol.154,p.1391    AnnalesdeChimie(Cachan,France),1915,vol.<9>4,p.300

[13]ChemicalCommunications,1997,p.127-128

[14]Synlett,2002,p.1843-1844

[15]OrganicLetters,2006,vol.8,p.5445-5448

[16]ChemicalCommunications,2003,p.1040-1041

[17]ChemicalCommunications,2008,p.1647-1649

[18]AngewandteChemie-InternationalEdition,2008,vol.47,p.9434-9438

[19]AdvancedSynthesisandCatalysis,2013,vol.355,p.880-884

[20]AngewandteChemie-InternationalEdition,2013,vol.52,p.7496-7499    Angew.Chem.,2013,vol.125,p.7644-7647,4

[21]Patent:WO2013/165662,2013,A1.Locationinpatent:Paragraph0083;0084

[22]CatalysisCommunications,2014,vol.45,p.25-29

[23]Chemistry-AEuropeanJournal,2014,vol.20,p.14488-14492

[24]ChemicalCommunications,2015,vol.51,p.7401-7404

[25]BulletinoftheKoreanChemicalSociety,2011,vol.32,p.3183-3186

[26]OrganicLetters,2016,vol.18,p.2463-2466

[27]AngewandteChemie-InternationalEdition,2017,vol.56,p.3585-3589    Angew.Chem.,2017,vol.129,p.3639-3643,5

[28]ChemicalCommunications,2017,vol.53,p.10390-10393

[29]ACSCatalysis,2017,vol.7,p.689-694

[30]AngewandteChemie-InternationalEdition,2018,vol.57,p.4970-4975    Angew.Chem.,2018,vol.130,p.5064-5069,6

[31]Catalysisscienceandtechnology,2018,vol.8,p.2648-2653

[32]AngewandteChemie-InternationalEdition,2018,vol.57,p.15177-15182    Angew.Chem.,2018,vol.130,p.15397-15402,6

[33]Chemistry-AEuropeanJournal,2019,vol.25,p.238-245

[34]AngewandteChemie-InternationalEdition,2019,vol.58,p.4356-4360    Angew.Chem.,2019,vol.131,p.4400-4404,5

[1]TetrahedronLetters,2004,vol.45,p.1965-1968

[2]Synlett,2015,vol.26,p.700-704

[3]TetrahedronLetters,2008,vol.49,p.1071-1075

[4]JournaloftheAmericanChemicalSociety,2001,vol.123,p.1365-1371

[5]AdvancedSynthesisandCatalysis,2006,vol.348,p.1734-1742

[6]TetrahedronLetters,2010,vol.51,p.808-810

[7]Tetrahedron,2010,vol.66,p.8536-8543

[8]OrganicLetters,2003,vol.5,p.185-187

[9]JournaloftheAmericanChemicalSociety,1999,vol.121,p.11229-11230

[10]Organicletters,2002,vol.4,p.2197-2199

[11]Phosphorus,SulfurandSiliconandtheRelatedElements,2008,vol.183,p.956-960

[12]BulletinoftheChemicalSocietyofJapan,1982,vol.55,p.3941-3942

[13]TetrahedronLetters,2011,vol.52,p.2540-2542

[14]JustusLiebigsAnnalenderChemie,1928,vol.467,p.231

[15]JournaloftheAmericanChemicalSociety,1959,vol.81,p.658,661

[16]Tetrahedron,1962,vol.18,p.751-761

[17]JournaloftheAmericanChemicalSociety,1961,vol.83,p.2329-2335

[18]Arzneimittel-Forschung/DrugResearch,2006,vol.56,p.346-350

[19]JournaloftheAmericanChemicalSociety,2011,vol.133,p.3658-3667

[20]EuropeanJournalofOrganicChemistry,2017,vol.2017,p.1502-1509

Title: Epoxidation of alkenes catalyzed by phenyl group-modified, periodic mesoporous organosilica-entrapped, dimeric manganese-salen complexes.

Journal: ChemSusChem 20111216

Title: Oxidative cleavage of alkenes using an in situ generated iodonium ion with oxone as a terminal oxidant.

Journal: Organic letters 20101217

Title: Intermolecular photocyclizations of N-(omega-hydroxyalkyl)tetrachlorophthalimide with alkenes leading to medium- and large-ring heterocycles--reaction modes and regio- and stereoselectivity of the 1,n-biradicals.

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Title: Structure-activity relationships of phenylcyclohexene and biphenyl antitubulin compounds against plant and mammalian cells.

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