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For: Pulakhandam SK, Katari NK, Manda RPR. Transition metal-promoted synthesis of 2-aryl/heteroaryl-thioquinazoline: C-S Bond formation by “Chan-Lam Cross-Coupling” Reaction. J Chem Sci 2017;129:203-10. [DOI: 10.1007/s12039-016-1217-7] [Cited by in Crossref: 14] [Cited by in F6Publishing: 15] [Article Influence: 2.3] [Reference Citation Analysis]
Number Citing Articles
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7 Chen J, Li J, Dong Z. A Review on the Latest Progress of Chan‐Lam Coupling Reaction. Adv Synth Catal 2020;362:3311-31. [DOI: 10.1002/adsc.202000495] [Cited by in Crossref: 89] [Cited by in F6Publishing: 94] [Article Influence: 29.7] [Reference Citation Analysis]
8 Fernandes RA, Bhowmik A, Yadav SS. Advances in Cu and Ni-catalyzed Chan–Lam-type coupling: synthesis of diarylchalcogenides, Ar 2 –X (X = S, Se, Te). Org Biomol Chem 2020;18:9583-600. [DOI: 10.1039/d0ob02035d] [Cited by in Crossref: 8] [Cited by in F6Publishing: 10] [Article Influence: 2.7] [Reference Citation Analysis]
9 Gudimella KK, Bonige KB, Gundla R, Katari NK, Yamajala B, Battula VR. 2,4‐Diphenyl‐1,2‐dihydroquinazoline Derivatives: Synthesis, Anticancer Activity and Docking Studies. ChemistrySelect 2019;4:12528-33. [DOI: 10.1002/slct.201902609] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
10 Liu X, Dong Z. Chemoselective Chan–Lam Coupling Reactions between Benzimidazoline-2-thiones and Arylboronic Acids. J Org Chem 2019;84:11524-32. [DOI: 10.1021/acs.joc.9b01370] [Cited by in Crossref: 17] [Cited by in F6Publishing: 21] [Article Influence: 4.3] [Reference Citation Analysis]
11 Liu X, Zhang S, Zhu H, Cheng Y, Peng H, Dong Z. An Efficient Chan-Lam S -Arylation of Arylthioureas with Arylboronic Acids: An Efficient Chan-Lam S -Arylation of Arylthioureas with Arylboronic Acids. Eur J Org Chem 2018;2018:4483-9. [DOI: 10.1002/ejoc.201800892] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 1.8] [Reference Citation Analysis]
12 Liu X, Zhu H, Zhang S, Cheng Y, Peng H, Dong Z. Facile synthesis of S -arylisothioureas via the S -arylation of arylthioureas with aryl iodides in water. Tetrahedron Letters 2018;59:3165-70. [DOI: 10.1016/j.tetlet.2018.07.012] [Cited by in Crossref: 12] [Cited by in F6Publishing: 11] [Article Influence: 2.4] [Reference Citation Analysis]
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