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For: Gogoi A, Guin S, Rajamanickam S, Rout SK, Patel BK. Synthesis of 1,2,4-Triazoles via Oxidative Heterocyclization: Selective C–N Bond Over C–S Bond Formation. J Org Chem 2015;80:9016-27. [DOI: 10.1021/acs.joc.5b00956] [Cited by in Crossref: 23] [Cited by in F6Publishing: 13] [Article Influence: 3.3] [Reference Citation Analysis]
Number Citing Articles
1 Singh SJ, Rajamanickam S, Gogoi A, Patel BK. Synthesis of 2-amino-substituted-1,3,4-thiadiazoles via 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) mediated intramolecular C–S bond formation in thiosemicarbazones. Tetrahedron Letters 2016;57:1044-7. [DOI: 10.1016/j.tetlet.2016.01.083] [Cited by in Crossref: 12] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
2 Zhu F, Yan Z, Ai C, Wang Y, Lin S. I 2 Promoted Synthesis of 2-Aminothiadiazoles Employing KSCN as a Sulfur Source Under Metal-Free Conditions: I 2 Promoted Synthesis of 2-Aminothiadiazoles Employing KSCN as a Sulfur Source Under Metal-Free Conditions. Eur J Org Chem 2019;2019:6561-5. [DOI: 10.1002/ejoc.201901250] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
3 Ji Ram V, Sethi A, Nath M, Pratap R. Five-Membered Heterocycles. The Chemistry of Heterocycles. Elsevier; 2019. pp. 149-478. [DOI: 10.1016/b978-0-08-101033-4.00005-x] [Cited by in Crossref: 14] [Article Influence: 4.7] [Reference Citation Analysis]
4 Kashyap A, Silakari O. Triazoles. Key Heterocycle Cores for Designing Multitargeting Molecules. Elsevier; 2018. pp. 323-42. [DOI: 10.1016/b978-0-08-102083-8.00009-1] [Cited by in Crossref: 2] [Article Influence: 0.5] [Reference Citation Analysis]
5 Matesanz AI, Herrero JM, Quiroga AG. Chemical and Biological Evaluation of Thiosemicarbazone-Bearing Heterocyclic Metal Complexes. Curr Top Med Chem 2021;21:59-72. [PMID: 33092510 DOI: 10.2174/1568026620666201022144004] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
6 Cui X, Liu X, Wang X, Tian W, Wei D, Huang G. Copper-Catalyzed ortho -Thiomethylation of Benzamides via 8-Aminoquinoline-Assisted C-H Activation with Dimethyl Sulfoxide. ChemistrySelect 2017;2:8607-11. [DOI: 10.1002/slct.201702046] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 1.2] [Reference Citation Analysis]
7 Aly AA, Hassan AA, Abdel-latief ESM. An Update of the Use of Thiocarbohydrazides and Thiosemicarbazides in the Preparation of Heterocycles and Their Biological Importance: Update on Heterocycles from Thiocarbohydrazides and Thiosemicarbazides. J Heterocyclic Chem 2018;55:2196-223. [DOI: 10.1002/jhet.3295] [Cited by in Crossref: 10] [Cited by in F6Publishing: 3] [Article Influence: 2.5] [Reference Citation Analysis]
8 Vidyacharan S, Murugan A, Sharada DS. C(sp(2))-H Functionalization of 2H-Indazoles at C3-Position via Palladium(II)-Catalyzed Isocyanide Insertion Strategy Leading to Diverse Heterocycles. J Org Chem 2016;81:2837-48. [PMID: 26954483 DOI: 10.1021/acs.joc.6b00048] [Cited by in Crossref: 47] [Cited by in F6Publishing: 30] [Article Influence: 7.8] [Reference Citation Analysis]
9 Baeten M, Maes BU. Carbon–Nitrogen Bond Formation Through Cross-Dehydrogenative Coupling Reactions. Elsevier; 2017. pp. 401-81. [DOI: 10.1016/bs.adomc.2017.04.003] [Cited by in Crossref: 11] [Cited by in F6Publishing: 4] [Article Influence: 2.2] [Reference Citation Analysis]
10 Jain A, Piplani P. Exploring the Chemistry and Therapeutic Potential of Triazoles: A Comprehensive Literature Review. MRMC 2019;19:1298-368. [DOI: 10.2174/1389557519666190312162601] [Cited by in Crossref: 8] [Cited by in F6Publishing: 7] [Article Influence: 2.7] [Reference Citation Analysis]
11 Pelivan K, Frensemeier L, Karst U, Koellensperger G, Bielec B, Hager S, Heffeter P, Keppler BK, Kowol CR. Understanding the metabolism of the anticancer drug Triapine: electrochemical oxidation, microsomal incubation and in vivo analysis using LC-HRMS. Analyst 2017;142:3165-76. [PMID: 28745337 DOI: 10.1039/c7an00902j] [Cited by in Crossref: 13] [Cited by in F6Publishing: 8] [Article Influence: 3.3] [Reference Citation Analysis]
12 Beyzaei H, Khosravi Z, Aryan R, Ghasemi B. A green one-pot synthesis of 3(5)-substituted 1,2,4-triazol-5(3)-amines as potential antimicrobial agents. J IRAN CHEM SOC 2019;16:2565-73. [DOI: 10.1007/s13738-019-01714-2] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 2.7] [Reference Citation Analysis]
13 Behera A, Rakshit A, Sahoo AK, Patel BK. One Pot Sequential Synthesis of N -[2-(Phenylsulfinyl)phenyl]acetamides: A Ring Opening Rearrangement Functionalization (RORF): One Pot Sequential Synthesis of N -[2-(Phenylsulfinyl)phenyl]acetamides: A Ring Opening Rearrangement Functionalization (RORF). Eur J Org Chem 2019;2019:1154-65. [DOI: 10.1002/ejoc.201801597] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
14 Ali W, Modi A, Behera A, Mohanta PR, Patel BK. Cs 2 CO 3 as a source of carbonyl and ethereal oxygen in a Cu-catalysed cascade synthesis of benzofuran [3,2-c] quinolin-6[5-H]ones. Org Biomol Chem 2016;14:5940-4. [DOI: 10.1039/c6ob01029f] [Cited by in Crossref: 9] [Article Influence: 1.5] [Reference Citation Analysis]
15 Tarai A, Baruah JB. Four-coordinated see-saw N -(aryl)-2-(propan-2-ylidene)hydrazinecarbothioamide complexes of nickel( ii ), copper( ii ) and zinc( ii ) and their propensity for catalytic cyclisation. Dalton Trans 2018;47:4921-30. [DOI: 10.1039/c8dt00453f] [Cited by in Crossref: 4] [Article Influence: 1.0] [Reference Citation Analysis]