C(5)—H arylation of 1-substituted 1,2,4-triazoles with aryl halides under Pd/NHC catalysis
An efficient method for the synthesis of 1-substituted 5-aryl-1,2,4-triazoles by selective C—H arylation of 1-substituted 1,2,4-triazoles with non-activated aryl chlorides and aryl bromides under the catalysis by a palladium complex with a N-heterocyclic carbene ligand IPr *OMe using 1,1,2,2-tetraph...
Saved in:
| Published in | Russian chemical bulletin Vol. 73; no. 4; pp. 950 - 956 |
|---|---|
| Main Authors | , , , |
| Format | Journal Article |
| Language | English |
| Published |
New York
Springer US
01.04.2024
Springer Nature B.V |
| Subjects | |
| Online Access | Get full text |
Cover
Loading…
| Abstract | An efficient method for the synthesis of 1-substituted 5-aryl-1,2,4-triazoles by selective C—H arylation of 1-substituted 1,2,4-triazoles with non-activated aryl chlorides and aryl bromides under the catalysis by a palladium complex with a N-heterocyclic carbene ligand IPr
*OMe
using 1,1,2,2-tetraphenylethane-1,2-diol (TPEDO) as a catalyst activator is reported. |
|---|---|
| AbstractList | An efficient method for the synthesis of 1-substituted 5-aryl-1,2,4-triazoles by selective C—H arylation of 1-substituted 1,2,4-triazoles with non-activated aryl chlorides and aryl bromides under the catalysis by a palladium complex with a N-heterocyclic carbene ligand IPr
*OMe
using 1,1,2,2-tetraphenylethane-1,2-diol (TPEDO) as a catalyst activator is reported. An efficient method for the synthesis of 1-substituted 5-aryl-1,2,4-triazoles by selective C—H arylation of 1-substituted 1,2,4-triazoles with non-activated aryl chlorides and aryl bromides under the catalysis by a palladium complex with a N-heterocyclic carbene ligand IPr*OMe using 1,1,2,2-tetraphenylethane-1,2-diol (TPEDO) as a catalyst activator is reported. |
| Author | Kutyrev, V. V. Chernenko, A. Yu Chernyshev, V. M. Astakhov, A. V. |
| Author_xml | – sequence: 1 givenname: A. V. surname: Astakhov fullname: Astakhov, A. V. organization: Platov South-Russian State Polytechnic University (NPI) – sequence: 2 givenname: A. Yu surname: Chernenko fullname: Chernenko, A. Yu organization: Platov South-Russian State Polytechnic University (NPI) – sequence: 3 givenname: V. V. surname: Kutyrev fullname: Kutyrev, V. V. organization: Platov South-Russian State Polytechnic University (NPI) – sequence: 4 givenname: V. M. surname: Chernyshev fullname: Chernyshev, V. M. email: chern13@yandex.ru organization: Platov South-Russian State Polytechnic University (NPI) |
| BookMark | eNp1kMFKAzEURYNUsK1-gLuAG4XG5mUmk2QpRa1Q1IXuhJDOZOyUcaYmGaSu_Ai_0C8xdQRXrt7jce593DtCg6ZtLELHQM-BUjH1ACAYoSwlKaOCqD00BC4SokDAIO40ywhnkh-gkfdrSimTUg7R0-yUn319fM6xcdvahKptcFtiIL5b-lCFLtgCw4RNUhJcZd7b2nr8VoXVD49Xpq6KeOmawjp8X0xv5zOcm2Dqra_8IdovTe3t0e8co8ery4fZnCzurm9mFwuSs0wGYplSVlhpGTXAixQSSDKRS5EsGZNKMsgzAFoKLgUrshi3BJlByiFRxVKYZIxOet-Na18764Net51r4kudUM6oBKaSSEFP5a713tlSb1z1EmNooHpXou5L1LFEvStRq6hhvcZHtnm27s_5f9E3WzFzbw |
| Cites_doi | 10.1021/ja805688p 10.1002/anie.201705785 10.1039/D0QI01411G 10.1039/C9DT03266E 10.1021/acs.chemrev.9b00634 10.1007/s11172-021-3065-y 10.1039/D2QI01832B 10.1021/jm100245q 10.1021/jo3021677 10.1039/D0TC00865F 10.1039/D0SC02629H 10.1002/jhet.5570120509 10.1021/acscatal.1c01929 10.1007/s11172-018-2277-2 10.1021/ja075802+ 10.1016/j.tetlet.2011.06.090 10.1021/ol0702324 10.1039/C6RA14670H 10.1007/s11172-022-3526-y 10.1021/acs.organomet.7b00184 10.1021/om9009203 10.1021/acs.jmedchem.9b00059 10.1021/acs.organomet.0c00260 10.1021/acs.oprd.2c00153 10.1007/s11172-022-3501-7 10.1007/s11172-018-2040-8 10.1039/C9CY02041A 10.1039/D1QI00453K 10.1039/C5SC02942B 10.1002/ejic.201300087 10.1021/acs.organomet.7b00669 10.1039/b922984a 10.1002/chem.202103341 10.1016/j.jorganchem.2019.121025 10.1007/s11172-021-3212-5 10.1021/jo00264a048 10.1021/om5001919 |
| ContentType | Journal Article |
| Copyright | Springer Science+Business Media LLC 2024 Springer Science+Business Media LLC 2024. |
| Copyright_xml | – notice: Springer Science+Business Media LLC 2024 – notice: Springer Science+Business Media LLC 2024. |
| DBID | AAYXX CITATION |
| DOI | 10.1007/s11172-024-4207-9 |
| DatabaseName | CrossRef |
| DatabaseTitle | CrossRef |
| DatabaseTitleList | |
| DeliveryMethod | fulltext_linktorsrc |
| Discipline | Chemistry |
| EISSN | 1573-9171 |
| EndPage | 956 |
| ExternalDocumentID | 10_1007_s11172_024_4207_9 |
| GroupedDBID | -4Y -58 -5G -BR -EM -Y2 -~C -~X .86 .VR 06C 06D 0R~ 0VY 123 1N0 2.D 28- 29P 2J2 2JN 2JY 2KG 2KM 2LR 2P1 2VQ 2~H 30V 4.4 406 408 409 40D 40E 53G 5QI 5VS 642 67Z 6NX 8TC 8UJ 95- 95. 95~ 96X AAAVM AABHQ AABYN AACDK AAEOY AAFGU AAGCJ AAHNG AAIAL AAIKT AAJBT AAJKR AANZL AARHV AARTL AASML AATNV AATVU AAUCO AAUYE AAWCG AAYIU AAYQN AAYTO ABAKF ABBBX ABBXA ABDZT ABECU ABFGW ABFTV ABHLI ABHQN ABJNI ABJOX ABKAS ABKCH ABKTR ABMNI ABMQK ABNWP ABQBU ABSXP ABTEG ABTHY ABTKH ABTMW ABULA ABWNU ABXPI ACAOD ACBMV ACBRV ACBXY ACBYP ACDTI ACGFS ACHSB ACHXU ACIGE ACIPQ ACIWK ACKNC ACMDZ ACMLO ACOKC ACOMO ACTTH ACVWB ACWMK ACZOJ ADHIR ADIMF ADINQ ADKNI ADKPE ADMDM ADOXG ADRFC ADTPH ADURQ ADYFF ADZKW AEBTG AEEQQ AEFIE AEFQL AEFTE AEGAL AEGNC AEJHL AEJRE AEKMD AEMSY AENEX AEOHA AEPYU AESKC AESTI AETLH AEVLU AEVTX AEXYK AFBBN AFEXP AFGCZ AFLOW AFNRJ AFQWF AFWTZ AFZKB AGAYW AGDGC AGGBP AGGDS AGJBK AGMZJ AGQEE AGQMX AGRTI AGWIL AGWZB AGYKE AHAVH AHBYD AHSBF AHYZX AIAKS AIGIU AIIXL AILAN AIMYW AITGF AJBLW AJDOV AJGSW AJRNO AKQUC ALMA_UNASSIGNED_HOLDINGS ALWAN AMKLP AMXSW AMYLF AOCGG ARMRJ AXYYD AZFZN B-. BA0 BBWZM BDATZ BGNMA CAG COF CS3 CSCUP DDRTE DL5 DNIVK DPUIP DU5 EBLON EBS EIOEI EJD ESBYG FEDTE FERAY FFXSO FIGPU FINBP FNLPD FRRFC FSGXE FWDCC G-Y G-Z GGCAI GGRSB GJIRD GNWQR GQ6 GQ7 GQ8 GXS HF~ HG6 HMJXF HQYDN HRMNR HVGLF HZ~ IHE IJ- IKXTQ IWAJR IXC IXD IXE IZIGR IZQ I~X I~Z J-C JBSCW JCJTX JZLTJ KDC KOV KOW LAK LLZTM M4Y MA- N2Q NB0 NDZJH NPVJJ NQJWS NU0 O9- O93 O9G O9I O9J OAM OVD P19 P9N PF0 PT4 PT5 QOK QOR QOS R89 R9I RHV RIG RNI RNS ROL RPX RSV RZC RZE RZK S16 S1Z S26 S27 S28 S3B SAP SCG SCLPG SCM SDH SDM SHX SISQX SJYHP SNE SNPRN SNX SOHCF SOJ SPISZ SQXTU SRMVM SSLCW STPWE SZN T13 T16 TEORI TSG TSK TSV TUC U2A UG4 UNUBA UOJIU UTJUX UZXMN VC2 VFIZW W23 W48 W4F WIP WJK WK8 XU3 YLTOR Z5O Z7R Z7S Z7U Z7V Z7W Z7X Z7Y Z7Z Z83 Z86 Z87 Z88 Z8M Z8N Z8O Z8P Z8Q Z8R Z8S Z8T Z8W Z8Z Z91 Z92 ZCG ZMTXR ~EX AAYXX AGJZZ CITATION |
| ID | FETCH-LOGICAL-c268t-e299e7e8e20a15d4131367c873b2289821c6110f75872d6007f186145139db7a3 |
| IEDL.DBID | U2A |
| ISSN | 1066-5285 |
| IngestDate | Fri Sep 13 03:13:45 EDT 2024 Thu Sep 12 19:49:31 EDT 2024 Wed May 08 01:14:36 EDT 2024 |
| IsPeerReviewed | true |
| IsScholarly | true |
| Issue | 4 |
| Keywords | palladium 1,2,4-triazole C—H arylation N-heterocyclic carbenes |
| Language | English |
| LinkModel | DirectLink |
| MergedId | FETCHMERGED-LOGICAL-c268t-e299e7e8e20a15d4131367c873b2289821c6110f75872d6007f186145139db7a3 |
| PQID | 3052081293 |
| PQPubID | 2043576 |
| PageCount | 7 |
| ParticipantIDs | proquest_journals_3052081293 crossref_primary_10_1007_s11172_024_4207_9 springer_journals_10_1007_s11172_024_4207_9 |
| PublicationCentury | 2000 |
| PublicationDate | 2024-04-01 |
| PublicationDateYYYYMMDD | 2024-04-01 |
| PublicationDate_xml | – month: 04 year: 2024 text: 2024-04-01 day: 01 |
| PublicationDecade | 2020 |
| PublicationPlace | New York |
| PublicationPlace_xml | – name: New York |
| PublicationTitle | Russian chemical bulletin |
| PublicationTitleAbbrev | Russ Chem Bull |
| PublicationYear | 2024 |
| Publisher | Springer US Springer Nature B.V |
| Publisher_xml | – name: Springer US – name: Springer Nature B.V |
| References | LiDOllevierTJ. Organomet. Chem.20209061210251:CAS:528:DC%2BC1MXit1Cmu7%2FJ10.1016/j.jorganchem.2019.121025 ClavierHNolanS PChem. Commun.2010468411:CAS:528:DC%2BC3cXhtFOitr0%3D10.1039/b922984a RomagnoliRBaraldiP GCruz-LopezOLopez CaraCCarrionM DBrancaleAHamelEChenLBortolozziRBassoGViolaGJ. Med. Chem.20105342481:CAS:528:DC%2BC3cXltFykt70%3D10.1021/jm100245q204204392887662 ChanK-TTsaiY-HLinW-SWuJ-RChenS-JLiaoF-XHuC-HLeeH MOrganometallics2010294631:CAS:528:DC%2BD1MXhs1WqsrzJ10.1021/om9009203 MutoKHatakeyamaTYamaguchiJItamiKChem. Sci.2015667921:CAS:528:DC%2BC2MXhsVGnu77E10.1039/C5SC02942B298619245951105 OuyangJ-SLiuSPanBZhangYLiangHChenBHeXChanW T KChanA S CSunT-YWuY-DQiuLACS Catal.20211192521:CAS:528:DC%2BB3MXhsFSrtrrP10.1021/acscatal.1c01929 PasyukovD VChernenkoA YLavrentevI VBaydikovaV AMinyaevM EStarovoytovaO AChernyshevV MRuss. Chem. Bull.2022719931:CAS:528:DC%2BB38XhtlOhsrfN10.1007/s11172-022-3501-7 NelsonD JColladoAManziniSMeiriesSSlawinA M ZCordesD BNolanS POrganometallics20143320481:CAS:528:DC%2BC2cXlvVClu74%3D10.1021/om5001919 ChernyshevV MDenisovaE AEreminD BAnanikovV PChem. Sci.20201169571:CAS:528:DC%2BB3cXhtlWktLnL10.1039/D0SC02629H331334867553045 AstakhovA VSolievS BGordeevE GChernyshevV MAnanikovV PDalton Trans.201948170521:CAS:528:DC%2BC1MXhvFOqtr3P10.1039/C9DT03266E31696883 TeciMBrennerEMattDToupetLEur. J. Inorg. Chem.2013201328411:CAS:528:DC%2BC3sXjslWrurs%3D10.1002/ejic.201300087 AstakhovA VChernenkoA YKutyrevV VRannyG SMinyaevM EChernyshevV MAnanikovV PInorg. Chem. Front.2023102181:CAS:528:DC%2BB38XivFaqu7nL10.1039/D2QI01832B ChernenkoA YAstakhovA VPasyukovD VDorovatovskiiP VZubavichusY VKhrustalevV NChernyshevV MRuss. Chem. Bull.201867791:CAS:528:DC%2BC1cXotFyrt74%3D10.1007/s11172-018-2040-8 ChesnokovV VShevchenkoM AAstakhovA VRuss. Chem. Bull.20227112471:CAS:528:DC%2BB38XhslSmtL%2FK10.1007/s11172-022-3526-y ShevchenkoM ATkachenkoY NAstakhovA VKhazipovO VTyurinR VPasyukovD VTafeenkoV AKravchenkoO AChernyshevV MRuss. Chem. Bull.20186716841:CAS:528:DC%2BC1cXitFKms7rJ10.1007/s11172-018-2277-2 GordeevE GEreminD BChernyshevV MAnanikovV POrganometallics2018377871:CAS:528:DC%2BC2sXhslKqtL7L10.1021/acs.organomet.7b00669 NguyenV HDangT TNguyenH HHuynhH VOrganometallics20203923091:CAS:528:DC%2BB3cXhtFWjsLvL10.1021/acs.organomet.0c00260 KhazipovO VShevchenkoM APasyukovD VChernenkoA YAstakhovA VTafeenkoV AChernyshevV MAnanikovV PCatal. Sci. Technol.20201012281:CAS:528:DC%2BC1MXit12hsb%2FK10.1039/C9CY02041A AstakhovA VKhazipovO VChernenkoA YPasyukovD VKashinA SGordeevE GKhrustalevV NChernyshevV MAnanikovV POrganometallics20173619811:CAS:528:DC%2BC2sXltlOls7c%3D10.1021/acs.organomet.7b00184 AstlefordB AGoeG LKeayJ GScrivenE F VJ. Org. Chem.1989547311:CAS:528:DyaL1MXnsFCisg%3D%3D10.1021/jo00264a048 DoH-QKhanR M KDaugulisOJ. Am. Chem. Soc.2008130151851:CAS:528:DC%2BD1cXht1CgsbfJ10.1021/ja805688p188554712740489 DoH-QDaugulisOJ. Am. Chem. Soc.2007129124041:CAS:528:DC%2BD2sXhtVKmsbnO10.1021/ja075802+178877622613793 MengGPengTShiYLiHWangXYinXYangD-TWangSWangSWangNJ. Mater. Chem. C2020877491:CAS:528:DC%2BB3cXnvVyhsbs%3D10.1039/D0TC00865F ChesnokovV VShevchenkoM ASolievS BTafeenkoV AChernyshevV MRuss. Chem. Bull.20217012811:CAS:528:DC%2BB3MXhslykt77N10.1007/s11172-021-3212-5 JamalZTeoY-CRSC Adv.20166754491:CAS:528:DC%2BC28Xht1ers7fI10.1039/C6RA14670H JooJ MGuoPSamesDJ. Org. Chem.2013787381:CAS:528:DC%2BC3sXitFek10.1021/jo302167723276283 ShepelenkoK ESolievS BGalushkoA SChernyshevV MAnanikovV PInorg. Chem. Front.2021815111:CAS:528:DC%2BB3MXhslWltr8%3D10.1039/D0QI01411G ChiongH ADaugulisOOrg. Lett.2007914491:CAS:528:DC%2BD2sXislKru70%3D10.1021/ol070232417358073 IschayM AHoangBSteinhuebelD PChinM RDixonD DElfgrenDHeumannLLewWMundalD ANevilleS TShahN PShiBTrippJ CWangQOrg. Process Res. Dev.20222626941:CAS:528:DC%2BB38XitFCnu7rP10.1021/acs.oprd.2c00153 GlushkovV ABabentzevD NDmitrievM VBorisovaI ADenisovM SRuss. Chem. Bull.2021701221:CAS:528:DC%2BB3MXkvVejt7k%3D10.1007/s11172-021-3065-y ZhaoQMengGNolanS PSzostakMChem. Rev.202012019811:CAS:528:DC%2BB3cXht1Klsbc%3D10.1021/acs.chemrev.9b00634319674517241961 BlairV LBlakemoreD CHayDHeviaEPrydeD CTetrahedron Lett.20115245901:CAS:528:DC%2BC3MXpvFWqtb0%3D10.1016/j.tetlet.2011.06.090 LiD-HLanX-BSongA-XRahmanM MXuCHuangF-DSzostakRSzostakMLiuF-SChem. — Eur. J.202228e2021033411:CAS:528:DC%2BB3MXis1KhsrfE10.1002/chem.20210334134773313 LiYHeYShaoTPeiHGuoWMiDKrimmIZhangYWangPWangXLiuMYiZChenYJ. Med. Chem.20196249491:CAS:528:DC%2BC1MXosVOhsLs%3D10.1021/acs.jmedchem.9b0005931026162 ChernenkoA YAstakhovA VKutyrevV VGordeevE GBurykinaJ VMinyaevM EKhrustalevV NChernyshevV MAnanikovV PInorg. Chem. Front.2021833821:CAS:528:DC%2BB3MXht12jtbjO10.1039/D1QI00453K KubotaSUdaMNakagawaTJ. Heterocycl. Chem.1975128551:CAS:528:DyaE28XivF2qug%3D%3D10.1002/jhet.5570120509 LiuLWangXWangNPengTWangSAngew. Chem., Int. Ed.20175691601:CAS:528:DC%2BC2sXhtVKhsbrI10.1002/anie.201705785 Y Li (4207_CR3) 2019; 62 O V Khazipov (4207_CR30) 2020; 10 A V Astakhov (4207_CR29) 2019; 48 D V Pasyukov (4207_CR37) 2022; 71 B A Astleford (4207_CR31) 1989; 54 H Clavier (4207_CR20) 2010; 46 J M Joo (4207_CR6) 2013; 78 A Y Chernenko (4207_CR19) 2018; 67 K Muto (4207_CR39) 2015; 6 H-Q Do (4207_CR9) 2008; 130 R Romagnoli (4207_CR33) 2010; 53 E G Gordeev (4207_CR28) 2018; 37 M Teci (4207_CR34) 2013; 2013 D J Nelson (4207_CR16) 2014; 33 H-Q Do (4207_CR8) 2007; 129 V A Glushkov (4207_CR36) 2021; 70 K Muto (4207_CR7) 2015; 6 V V Chesnokov (4207_CR25) 2022; 71 Q Zhao (4207_CR18) 2020; 120 L Liu (4207_CR11) 2017; 56 K-T Chan (4207_CR35) 2010; 29 H A Chiong (4207_CR4) 2007; 9 J-S Ouyang (4207_CR15) 2021; 11 V M Chernyshev (4207_CR27) 2020; 11 K E Shepelenko (4207_CR23) 2021; 8 R Romagnoli (4207_CR2) 2010; 53 D-H Li (4207_CR13) 2022; 28 M A Shevchenko (4207_CR17) 2018; 67 A Y Chernenko (4207_CR26) 2021; 8 A V Astakhov (4207_CR32) 2017; 36 A V Astakhov (4207_CR14) 2023; 10 Z Jamal (4207_CR10) 2016; 6 M A Ischay (4207_CR1) 2022; 26 V H Nguyen (4207_CR22) 2020; 39 V V Chesnokov (4207_CR24) 2021; 70 D Li (4207_CR21) 2020; 906 G Meng (4207_CR12) 2020; 8 S Kubota (4207_CR38) 1975; 12 V L Blair (4207_CR5) 2011; 52 |
| References_xml | – volume: 130 start-page: 15185 year: 2008 ident: 4207_CR9 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja805688p contributor: fullname: H-Q Do – volume: 56 start-page: 9160 year: 2017 ident: 4207_CR11 publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201705785 contributor: fullname: L Liu – volume: 8 start-page: 1511 year: 2021 ident: 4207_CR23 publication-title: Inorg. Chem. Front. doi: 10.1039/D0QI01411G contributor: fullname: K E Shepelenko – volume: 48 start-page: 17052 year: 2019 ident: 4207_CR29 publication-title: Dalton Trans. doi: 10.1039/C9DT03266E contributor: fullname: A V Astakhov – volume: 120 start-page: 1981 year: 2020 ident: 4207_CR18 publication-title: Chem. Rev. doi: 10.1021/acs.chemrev.9b00634 contributor: fullname: Q Zhao – volume: 70 start-page: 122 year: 2021 ident: 4207_CR36 publication-title: Russ. Chem. Bull. doi: 10.1007/s11172-021-3065-y contributor: fullname: V A Glushkov – volume: 10 start-page: 218 year: 2023 ident: 4207_CR14 publication-title: Inorg. Chem. Front. doi: 10.1039/D2QI01832B contributor: fullname: A V Astakhov – volume: 53 start-page: 4248 year: 2010 ident: 4207_CR2 publication-title: J. Med. Chem. doi: 10.1021/jm100245q contributor: fullname: R Romagnoli – volume: 78 start-page: 738 year: 2013 ident: 4207_CR6 publication-title: J. Org. Chem. doi: 10.1021/jo3021677 contributor: fullname: J M Joo – volume: 8 start-page: 7749 year: 2020 ident: 4207_CR12 publication-title: J. Mater. Chem. C doi: 10.1039/D0TC00865F contributor: fullname: G Meng – volume: 11 start-page: 6957 year: 2020 ident: 4207_CR27 publication-title: Chem. Sci. doi: 10.1039/D0SC02629H contributor: fullname: V M Chernyshev – volume: 12 start-page: 855 year: 1975 ident: 4207_CR38 publication-title: J. Heterocycl. Chem. doi: 10.1002/jhet.5570120509 contributor: fullname: S Kubota – volume: 11 start-page: 9252 year: 2021 ident: 4207_CR15 publication-title: ACS Catal. doi: 10.1021/acscatal.1c01929 contributor: fullname: J-S Ouyang – volume: 67 start-page: 1684 year: 2018 ident: 4207_CR17 publication-title: Russ. Chem. Bull. doi: 10.1007/s11172-018-2277-2 contributor: fullname: M A Shevchenko – volume: 129 start-page: 12404 year: 2007 ident: 4207_CR8 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja075802+ contributor: fullname: H-Q Do – volume: 52 start-page: 4590 year: 2011 ident: 4207_CR5 publication-title: Tetrahedron Lett. doi: 10.1016/j.tetlet.2011.06.090 contributor: fullname: V L Blair – volume: 53 start-page: 4248 year: 2010 ident: 4207_CR33 publication-title: J. Med. Chem. doi: 10.1021/jm100245q contributor: fullname: R Romagnoli – volume: 9 start-page: 1449 year: 2007 ident: 4207_CR4 publication-title: Org. Lett. doi: 10.1021/ol0702324 contributor: fullname: H A Chiong – volume: 6 start-page: 75449 year: 2016 ident: 4207_CR10 publication-title: RSC Adv. doi: 10.1039/C6RA14670H contributor: fullname: Z Jamal – volume: 71 start-page: 1247 year: 2022 ident: 4207_CR25 publication-title: Russ. Chem. Bull. doi: 10.1007/s11172-022-3526-y contributor: fullname: V V Chesnokov – volume: 36 start-page: 1981 year: 2017 ident: 4207_CR32 publication-title: Organometallics doi: 10.1021/acs.organomet.7b00184 contributor: fullname: A V Astakhov – volume: 29 start-page: 463 year: 2010 ident: 4207_CR35 publication-title: Organometallics doi: 10.1021/om9009203 contributor: fullname: K-T Chan – volume: 62 start-page: 4949 year: 2019 ident: 4207_CR3 publication-title: J. Med. Chem. doi: 10.1021/acs.jmedchem.9b00059 contributor: fullname: Y Li – volume: 39 start-page: 2309 year: 2020 ident: 4207_CR22 publication-title: Organometallics doi: 10.1021/acs.organomet.0c00260 contributor: fullname: V H Nguyen – volume: 26 start-page: 2694 year: 2022 ident: 4207_CR1 publication-title: Org. Process Res. Dev. doi: 10.1021/acs.oprd.2c00153 contributor: fullname: M A Ischay – volume: 71 start-page: 993 year: 2022 ident: 4207_CR37 publication-title: Russ. Chem. Bull. doi: 10.1007/s11172-022-3501-7 contributor: fullname: D V Pasyukov – volume: 67 start-page: 79 year: 2018 ident: 4207_CR19 publication-title: Russ. Chem. Bull. doi: 10.1007/s11172-018-2040-8 contributor: fullname: A Y Chernenko – volume: 10 start-page: 1228 year: 2020 ident: 4207_CR30 publication-title: Catal. Sci. Technol. doi: 10.1039/C9CY02041A contributor: fullname: O V Khazipov – volume: 8 start-page: 3382 year: 2021 ident: 4207_CR26 publication-title: Inorg. Chem. Front. doi: 10.1039/D1QI00453K contributor: fullname: A Y Chernenko – volume: 6 start-page: 6792 year: 2015 ident: 4207_CR7 publication-title: Chem. Sci. doi: 10.1039/C5SC02942B contributor: fullname: K Muto – volume: 2013 start-page: 2841 year: 2013 ident: 4207_CR34 publication-title: Eur. J. Inorg. Chem. doi: 10.1002/ejic.201300087 contributor: fullname: M Teci – volume: 37 start-page: 787 year: 2018 ident: 4207_CR28 publication-title: Organometallics doi: 10.1021/acs.organomet.7b00669 contributor: fullname: E G Gordeev – volume: 46 start-page: 841 year: 2010 ident: 4207_CR20 publication-title: Chem. Commun. doi: 10.1039/b922984a contributor: fullname: H Clavier – volume: 28 start-page: e202103341 year: 2022 ident: 4207_CR13 publication-title: Chem. — Eur. J. doi: 10.1002/chem.202103341 contributor: fullname: D-H Li – volume: 906 start-page: 121025 year: 2020 ident: 4207_CR21 publication-title: J. Organomet. Chem. doi: 10.1016/j.jorganchem.2019.121025 contributor: fullname: D Li – volume: 70 start-page: 1281 year: 2021 ident: 4207_CR24 publication-title: Russ. Chem. Bull. doi: 10.1007/s11172-021-3212-5 contributor: fullname: V V Chesnokov – volume: 6 start-page: 6792 year: 2015 ident: 4207_CR39 publication-title: Chem. Sci. doi: 10.1039/C5SC02942B contributor: fullname: K Muto – volume: 54 start-page: 731 year: 1989 ident: 4207_CR31 publication-title: J. Org. Chem. doi: 10.1021/jo00264a048 contributor: fullname: B A Astleford – volume: 33 start-page: 2048 year: 2014 ident: 4207_CR16 publication-title: Organometallics doi: 10.1021/om5001919 contributor: fullname: D J Nelson |
| SSID | ssj0002888 |
| Score | 2.3687828 |
| Snippet | An efficient method for the synthesis of 1-substituted 5-aryl-1,2,4-triazoles by selective C—H arylation of 1-substituted 1,2,4-triazoles with non-activated... |
| SourceID | proquest crossref springer |
| SourceType | Aggregation Database Publisher |
| StartPage | 950 |
| SubjectTerms | Aromatic compounds Bromides Catalysis Chemistry Chemistry and Materials Science Chemistry/Food Science Full Articles Halides Inorganic Chemistry Organic Chemistry Palladium Substitutes Triazoles |
| Title | C(5)—H arylation of 1-substituted 1,2,4-triazoles with aryl halides under Pd/NHC catalysis |
| URI | https://link.springer.com/article/10.1007/s11172-024-4207-9 https://www.proquest.com/docview/3052081293/abstract/ |
| Volume | 73 |
| hasFullText | 1 |
| inHoldings | 1 |
| isFullTextHit | |
| isPrint | |
| link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV3LSgMxFL3UdqEb8YnVWrJw4aPRJpPJpMsytA6KxYWFCsKQmaQIQittXejKj_AL_RJzZzotii7czoQsbpJ7zn0DHDmK4AlpPSpsIqjQMqXaTzDBhqXaZ9IwjtXINz0Z9cXVwB-UgC9cF6On8yIimSnqZa0bc1hLHaRQwZsBba1ABbkD3uQ-by-0L1cqL3-T0hlZyi8imb9t8R2LlgTzR0w0g5ruBqzPOSJp54e6CSU72oLVsBjNtg0P4bF_8vn-ERE9ec2T2ch4SBidOjWQx_4NYQ3eEBSncrxh0yaCHtdsPXl03Nu4L1g_NiG35qIXhSTz42B7kh3odzt3YUTnYxJoyqWaUesQxQZWWd7UzDcOlbANW6oCL-HOnFKcpdKB_NBZBgE32I9-yJTECb1eyySB9nahPBqP7B6QIDFMa5tIRxpESzNlnQGrjGbcCmPToAqnhcDi57wbRrzse4zSjZ10Y5Ru3KpCrRBpPH8Y09jDvBuFJKMKZ4WYl7__3Gz_X6sPYI3jMWcZNjUozyYv9tCRh1lSh0r78v66U89uzRe8Cbna |
| link.rule.ids | 315,786,790,27957,27958,41116,41558,42185,42627,52146,52269 |
| linkProvider | Springer Nature |
| linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV07T8MwELagDGVBPEWhgAcGHrWoHcdxxiqiCtBWDK3UAclyYldMLWrLABM_gl_IL8GXBxEIBtbE8nBO7vvOd_cdQqeOInhcWI9wm3DCtUiJ9hMosKGp9qkwlEE3cn8g4hG_Hfvjoo97UVa7lynJzFNXzW7UgS1xmEI4awckXEVrIKcOEdeIdb7cL5My738TwkVZ0i9Tmb9t8R2MKob5IymaYU13E20UJBF38lPdQit2uo3qUTmbbQc9RGf--cfbe4z1_CWvZsOzCaZk4fxAnvw3mLZYixMYy_EKqk0Yrlyz9fjRkW_jnkAD2Rzfm6tBHOHsIgf0SXbRqHs9jGJSzEkgKRNySayDFBtYaVlbU984WAIdtlQGXsJcPCUZTYVD-YkLDQJmQJB-QqWAEb1eaJJAe3uoNp1N7T7CQWKo1jYRjjXwUFNpXQQrjabMcmPToIEuSoOpp1wOQ1XCx2Bd5ayrwLoqbKBmaVJV_BkL5UHhjQSW0UCXpZmr139udvCv1SeoHg_7PdW7GdwdonUGR56V2zRRbTl_tkeOSSyT4-zL-QTdEbuh |
| linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV27TsMwFLWgSMCCeIpCAQ8MvKzWjuM4Y1WowqvqQKUOSJETO2JKqzYMMPERfCFfgm8eRCAYWBPLw3Xic6597rkIHVuK4HBhHMJNxAlXIibKjUBgQ2PlUqEpg2rk-4EIRvxm7I7LPqfzSu1eXUkWNQ3g0pRm7alO2nXhG7XASyy-EM46HvEX0RIgI2i6Rqz7tRUzKYtaOCFsxiXd6lrztym-A1PNNn9ckOa4019HayVhxN1ihTfQgkk30Uqv6tO2hR57J-7px9t7gNXspVC24UmCKZnbPaEQAmhML9gFJ9Ci4xUcnDAcv-bj8ZMl4to-gWKyGR7q9iDo4fxQB7xKttGof_XQC0jZM4HETMiMGAsvxjPSsI6irrYQBZ5ssfSciNncSjIaC4v4iU0TPKbBnD6hUkC7XsfXkaecHdRIJ6nZRdiLNFXKRMIyCO4rKo3NZqVWlBmuTew10VkVsHBaWGOEtQkyRDe00Q0huqHfRK0qpGH5l8xDB0Q4EhhHE51XYa5f_znZ3r9GH6Hl4WU_vLse3O6jVQYrnitvWqiRzZ7NgSUVWXSYfzifROW_5g |
| openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=C%285%29%E2%80%94H+arylation+of+1-substituted+1%2C2%2C4-triazoles+with+aryl+halides+under+Pd%2FNHC+catalysis&rft.jtitle=Russian+chemical+bulletin&rft.au=Astakhov%2C+A.+V.&rft.au=Chernenko%2C+A.+Yu&rft.au=Kutyrev%2C+V.+V.&rft.au=Chernyshev%2C+V.+M.&rft.date=2024-04-01&rft.pub=Springer+US&rft.issn=1066-5285&rft.eissn=1573-9171&rft.volume=73&rft.issue=4&rft.spage=950&rft.epage=956&rft_id=info:doi/10.1007%2Fs11172-024-4207-9&rft.externalDocID=10_1007_s11172_024_4207_9 |
| thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1066-5285&client=summon |
| thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1066-5285&client=summon |
| thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1066-5285&client=summon |