BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Ueda S, Su M, Buchwald SL. Highly N2-Selective Palladium-Catalyzed Arylation of 1,2,3-Triazoles. Angew Chem 2011;123:9106-9. [DOI: 10.1002/ange.201103882] [Cited by in Crossref: 32] [Cited by in F6Publishing: 23] [Article Influence: 2.9] [Reference Citation Analysis]
Number Citing Articles
1 Liu W, Li Y, Wang Y, Kuang C. Site-Selective Direct Arylation of 1,2,3-Triazole N -Oxides: Site-Selective Direct Arylation of 1,2,3-Triazole N -Oxides. Eur J Org Chem 2013;2013:5272-5. [DOI: 10.1002/ejoc.201300747] [Cited by in Crossref: 23] [Cited by in F6Publishing: 10] [Article Influence: 2.6] [Reference Citation Analysis]
2 Paradies J. Palladium-Catalyzed Aromatic Carbon-Nitrogen Bond Formation. In: de Meijere A, Bräse S, Oestreich M, editors. Metal-Catalyzed Cross-Coupling Reactions and More. Weinheim: Wiley-VCH Verlag GmbH & Co. KGaA; 2014. pp. 995-1066. [DOI: 10.1002/9783527655588.ch13] [Cited by in Crossref: 3] [Article Influence: 0.3] [Reference Citation Analysis]
3 Jacq J, Pasau P. Multistep Flow Synthesis of 5-Amino-2-aryl-2 H -[1,2,3]-triazole-4-carbonitriles. Chem Eur J 2014;20:12223-33. [DOI: 10.1002/chem.201402074] [Cited by in Crossref: 15] [Cited by in F6Publishing: 12] [Article Influence: 1.9] [Reference Citation Analysis]
4 Kommu N, Kumar AS, Raveendra J, Ghule VD, Sahoo AK. Synthesis, Characterization, and Energetic Studies of Polynitro Aryl-1,2,3-2 H -Triazoles. Asian J Org Chem 2016;5:138-46. [DOI: 10.1002/ajoc.201500390] [Cited by in Crossref: 11] [Article Influence: 1.6] [Reference Citation Analysis]
5 Xu K, Thieme N, Breit B. Unlocking the N2 Selectivity of Benzotriazoles: Regiodivergent and Highly Selective Coupling of Benzotriazoles with Allenes. Angew Chem 2014;126:7396-9. [DOI: 10.1002/ange.201403682] [Cited by in Crossref: 46] [Cited by in F6Publishing: 40] [Article Influence: 5.8] [Reference Citation Analysis]
6 Wei H, Hu Q, Ma Y, Wei L, Liu J, Shi M, Wang F. Highly N 2 -Regioselective TsOH-Catalyzed Olefin Hydroamination: Metal-Free Synthesis of N2 -Alkyl-1,2,3-triazoles. Asian J Org Chem 2017;6:662-5. [DOI: 10.1002/ajoc.201700045] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 0.8] [Reference Citation Analysis]
7 Rao DN, Rasheed S, Kumar KA, Reddy AS, Das P. Copper-Catalyzed CNH 2 Arylation of 2-Aminobenzimidazoles and Related C-Amino-NH-azoles. Adv Synth Catal 2016;358:2126-33. [DOI: 10.1002/adsc.201600035] [Cited by in Crossref: 30] [Cited by in F6Publishing: 20] [Article Influence: 5.0] [Reference Citation Analysis]
8 Shi S, Buchwald SL. Palladium-Catalyzed Intramolecular CH Difluoroalkylation: Synthesis of Substituted 3,3-Difluoro-2-oxindoles. Angew Chem 2015;127:1666-70. [DOI: 10.1002/ange.201410471] [Cited by in Crossref: 25] [Cited by in F6Publishing: 22] [Article Influence: 3.1] [Reference Citation Analysis]
9 Li Z, Wei Q, Song L, Han W, Wu X, Zhao Y, Xia F, Liu S. Highly Regioselective Radical Transformation of N -Sulfonyl-1,2,3-triazoles in Air. Org Lett 2019;21:6413-7. [DOI: 10.1021/acs.orglett.9b02269] [Cited by in Crossref: 14] [Cited by in F6Publishing: 4] [Article Influence: 4.7] [Reference Citation Analysis]
10 Hu L, Mück-lichtenfeld C, Wang T, He G, Gao M, Zhao J. Reaction between Azidyl Radicals and Alkynes: A Straightforward Approach to NH -1,2,3-Triazoles. Chem Eur J 2016;22:911-5. [DOI: 10.1002/chem.201504515] [Cited by in Crossref: 21] [Cited by in F6Publishing: 14] [Article Influence: 3.0] [Reference Citation Analysis]
11 Liu L, Ai Y, Li D, Qi L, Zhou J, Tang Z, Shao Z, Liang Q, Sun H. Recyclable Acid-Base Bifunctional Core-Shell-Shell Nanosphere Catalyzed Synthesis of 5-Aryl-1 H -1,2,3-triazoles through the “One-Pot” Cyclization of Aldehydes, Nitromethane, and Sodium Azide. ChemCatChem 2017;9:3131-7. [DOI: 10.1002/cctc.201700401] [Cited by in Crossref: 20] [Article Influence: 4.0] [Reference Citation Analysis]
12 Wen J, Zhu L, Bi Q, Shen Z, Li X, Li X, Wang Z, Chen Z. Highly N 2 -Selective Coupling of 1,2,3-Triazoles with Indole and Pyrrole. Chem Eur J 2014;20:974-8. [DOI: 10.1002/chem.201302761] [Cited by in Crossref: 33] [Cited by in F6Publishing: 23] [Article Influence: 3.7] [Reference Citation Analysis]
13 Li L, Jiang Y, Hao J, Wei Y, Shi M. N2 -Selective Autocatalytic Ditriazolylation Reactions of Cyclopropenones and Tropone with N1 -Sulfonyl-1,2,3-triazoles. Adv Synth Catal 2017;359:3304-10. [DOI: 10.1002/adsc.201700936] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 1.6] [Reference Citation Analysis]
14 Kumar AS, Ghule VD, Subrahmanyam S, Sahoo AK. Synthesis of Thermally Stable Energetic 1,2,3-Triazole Derivatives. Chem Eur J 2013;19:509-18. [DOI: 10.1002/chem.201203192] [Cited by in Crossref: 48] [Cited by in F6Publishing: 29] [Article Influence: 4.8] [Reference Citation Analysis]
15 Chen H, Yi H, Tang Z, Bian C, Zhang H, Lei A. External Oxidant-Free Regioselective Cross Dehydrogenative Coupling of 2-Arylimidazoheterocycles and Azoles with H 2 Evolution via Photoredox Catalysis. Adv Synth Catal 2018;360:3220-7. [DOI: 10.1002/adsc.201800531] [Cited by in Crossref: 34] [Cited by in F6Publishing: 20] [Article Influence: 8.5] [Reference Citation Analysis]
16 Ueda S, Buchwald SL. Catalyst-Controlled Chemoselective Arylation of 2-Aminobenzimidazoles. Angew Chem 2012;124:10510-3. [DOI: 10.1002/ange.201204710] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 1.1] [Reference Citation Analysis]
17 Xu K, Thieme N, Breit B. Unlocking the N2 Selectivity of Benzotriazoles: Regiodivergent and Highly Selective Coupling of Benzotriazoles with Allenes. Angew Chem Int Ed 2014;53:7268-71. [DOI: 10.1002/anie.201403682] [Cited by in Crossref: 91] [Cited by in F6Publishing: 76] [Article Influence: 11.4] [Reference Citation Analysis]
18 Chen M, Buchwald SL. Continuous-Flow Synthesis of 1 - Substituted Benzotriazoles from Chloronitrobenzenes and Amines in a CN Bond Formation/Hydrogenation/Diazotization/Cyclization Sequence. Angew Chem Int Ed 2013;52:4247-50. [DOI: 10.1002/anie.201300615] [Cited by in Crossref: 74] [Cited by in F6Publishing: 58] [Article Influence: 8.2] [Reference Citation Analysis]
19 Motornov VA, Tabolin AA, Novikov RA, Nelyubina YV, Ioffe SL, Smolyar IV, Nenajdenko VG. Synthesis and Regioselective N-2 Functionalization of 4-Fluoro-5-aryl-1,2,3-N H -triazoles: Synthesis and Regioselective N-2 Functionalization of 4-Fluoro-5-aryl-1,2,3-N H -triazoles. Eur J Org Chem 2017;2017:6851-60. [DOI: 10.1002/ejoc.201701338] [Cited by in Crossref: 22] [Cited by in F6Publishing: 9] [Article Influence: 4.4] [Reference Citation Analysis]
20 Ramachary DB, Shashank AB. Organocatalytic Triazole Formation, Followed by Oxidative Aromatization: Regioselective Metal-Free Synthesis of Benzotriazoles. Chem Eur J 2013;19:13175-81. [DOI: 10.1002/chem.201301412] [Cited by in Crossref: 103] [Cited by in F6Publishing: 83] [Article Influence: 11.4] [Reference Citation Analysis]
21 Hu Q, Liu Y, Deng X, Li Y, Chen Y. Aluminium(III) Chloride-Catalyzed Three-Component Condensation of Aromatic Aldehydes, Nitroalkanes and Sodium Azide for the Synthesis of 4-Aryl- NH -1,2,3-triazoles. Adv Synth Catal 2016;358:1689-93. [DOI: 10.1002/adsc.201600098] [Cited by in Crossref: 51] [Cited by in F6Publishing: 23] [Article Influence: 8.5] [Reference Citation Analysis]
22 Chen C, Lu X, Holland MC, Lv S, Ji X, Liu W, Liu J, Depre D, Westerduin P. Synthesis of 2-Substituted 1,2,3-Triazoles via an Intramolecular N - N Bond Formation: Synthesis of 2-Substituted 1,2,3-Triazoles via an Intramolecular N - N Bond Formation. Eur J Org Chem 2020;2020:548-51. [DOI: 10.1002/ejoc.201901519] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
23 Chen M, Buchwald SL. Continuous-Flow Synthesis of 1 - Substituted Benzotriazoles from Chloronitrobenzenes and Amines in a CN Bond Formation/Hydrogenation/Diazotization/Cyclization Sequence. Angew Chem 2013;125:4341-4. [DOI: 10.1002/ange.201300615] [Cited by in Crossref: 23] [Cited by in F6Publishing: 17] [Article Influence: 2.6] [Reference Citation Analysis]
24 Roshandel S, Lunn MJ, Rasul G, Muthiah Ravinson DS, Suri SC, Prakash GKS. Catalyst-Free Regioselective N2 Arylation of 1,2,3-Triazoles Using Diaryl Iodonium Salts. Org Lett 2019;21:6255-8. [PMID: 31386386 DOI: 10.1021/acs.orglett.9b02140] [Cited by in Crossref: 13] [Cited by in F6Publishing: 7] [Article Influence: 4.3] [Reference Citation Analysis]
25 Zhang H, Jing L, Zheng Y, Sang R, Zhao Y, Wang Q, Wu Y. Rhodium-Catalyzed ortho -Cyanation of 2-Aryl-1,2,3-triazole: An Alternative Approach to Suvorexant: Rhodium-Catalyzed ortho -Cyanation of 2-Aryl-1,2,3-triazole: An Alternative Approach to Suvorexant. Eur J Org Chem 2018;2018:723-9. [DOI: 10.1002/ejoc.201701476] [Cited by in Crossref: 16] [Cited by in F6Publishing: 9] [Article Influence: 4.0] [Reference Citation Analysis]
26 Senecal TD, Shu W, Buchwald SL. A General, Practical Palladium-Catalyzed Cyanation of (Hetero)Aryl Chlorides and Bromides. Angew Chem 2013;125:10219-23. [DOI: 10.1002/ange.201304188] [Cited by in Crossref: 25] [Cited by in F6Publishing: 22] [Article Influence: 2.8] [Reference Citation Analysis]
27 Rai V, P K, Harmalkar SS, Dhuri SN, Maddani MR. 1,6-Addition of 1,2,3-NH triazoles to para-quinone methides: Facile access to highly selective N1 and N2 substituted triazoles. Org Biomol Chem 2022;20:345-51. [PMID: 34908078 DOI: 10.1039/d1ob01717a] [Reference Citation Analysis]