BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Tian L, Lu S, Zhang Z, Huang E, Yan H, Zhu X, Hao X, Song M. Copper-Catalyzed Double Thiolation To Access Sulfur-Bridged Imidazopyridines with Isothiocyanate. J Org Chem 2019;84:5213-21. [DOI: 10.1021/acs.joc.9b00186] [Cited by in Crossref: 27] [Cited by in F6Publishing: 15] [Article Influence: 9.0] [Reference Citation Analysis]
Number Citing Articles
1 Zhong P, Wu J, Wu J, Liu K, Wan C, Liu J. Solvent-controlled selective synthesis of amides and thioureas from isothiocyanates. Tetrahedron Letters 2022. [DOI: 10.1016/j.tetlet.2022.154099] [Reference Citation Analysis]
2 Shi L, Li T, Mei G. Recent advances in transition-metal-free C–H functionalization of imidazo[1,2-a]pyridines. Green Synthesis and Catalysis 2022. [DOI: 10.1016/j.gresc.2022.03.007] [Reference Citation Analysis]
3 Laxmikeshav K, Sakla AP, John SE, Shankaraiah N. One-pot, microwave-assisted copper( i )-catalysed dithiocarbamation: facile introduction of dithiocarbamate on imidazopyridines. Green Chem . [DOI: 10.1039/d1gc03952k] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
4 Reddy RJ, Shankar A, Kumar JJ, Sharadha N, Krishna GR. Diethyl phosphite-mediated switchable synthesis of bis(imidazoheterocycles) derived disulfanes and sulfanes using imidazoheterocycles and octasulfur. New J Chem 2022;46:4784-91. [DOI: 10.1039/d1nj05226h] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Shi T, Liu Y, Wang S, Lv Q, Yu B. Recyclable Carbon Nitride Nanosheet‐Photocatalyzed Aminomethylation of Imidazo[1,2‐ a ]pyridines in Green Solvent. Chin J Chem 2022;40:97-103. [DOI: 10.1002/cjoc.202100444] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 5.0] [Reference Citation Analysis]
6 Li T, Zhu X, Jiang H, Wang Y, Zheng N, Peng T, Gao R, Shi L, Hao X, Song M. Pd‐catalyzed decarboxylative [3 + 2] cycloaddition: Assembly of highly functionalized spirooxindoles bearing two quaternary centers. Appl Organomet Chem. [DOI: 10.1002/aoc.6516] [Reference Citation Analysis]
7 Tali JA, Kumar G, Singh D, Shankar R. Palladium(II) catalyzed site-selective C-H olefination of imidazo[1,2-a]pyridines. Org Biomol Chem 2021;19:9401-6. [PMID: 34705920 DOI: 10.1039/d1ob01683k] [Reference Citation Analysis]
8 Ghosh D, Ghosh S, Hajra A. Electrochemical Functionalization of Imidazopyridine and Indazole: An Overview. Adv Synth Catal 2021;363:5047-71. [DOI: 10.1002/adsc.202100981] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
9 Jiang H, Shen H, Zhu S, Wang B, Yang Y, Nong Z, Yi M, Tang S, Gui QW. Diethylaminosulfur Trifluoride: A Novel, Low-Cost, Stable Double Thiolation Reagent for Imidazo[1,2-α]pyridines. ACS Omega 2021;6:26273-81. [PMID: 34660986 DOI: 10.1021/acsomega.1c03291] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
10 Xue Y, Shi L, Wang X, Yu X, Zhu X, Hao XQ, Song MP. Regioselective N-F and α C(sp3)-H Arylation of Aliphatic N-Fluorosulfonamides with Imidazopyridines. Org Lett 2021;23:6807-12. [PMID: 34406015 DOI: 10.1021/acs.orglett.1c02381] [Reference Citation Analysis]
11 Tiekink ER. Supramolecular aggregation patterns featuring Se⋯N secondary-bonding interactions in mono-nuclear selenium compounds: A comparison with their congeners. Coordination Chemistry Reviews 2021;443:214031. [DOI: 10.1016/j.ccr.2021.214031] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 8.0] [Reference Citation Analysis]
12 Ma ST, Zhu XX, Xu JY, Li Y, Zhang XM, Feng CT, Yan Y. Iodide-promoted transformations of imidazopyridines into sulfur-bridged imidazopyridines or 1,2,4-thiadiazoles. Chem Commun (Camb) 2021;57:5338-41. [PMID: 33928973 DOI: 10.1039/d1cc01044a] [Reference Citation Analysis]
13 Gan Z, Zhu X, Yan Q, Song X, Yang D. Oxidative dual C–H sulfenylation: A strategy for the synthesis of bis(imidazo[1,2-a]pyridin-3-yl)sulfanes under metal-free conditions using sulfur powder. Chinese Chemical Letters 2021;32:1705-8. [DOI: 10.1016/j.cclet.2020.12.046] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
14 Konwar D, Bora U. Recent Developments in Transition‐Metal‐Catalyzed Regioselective Functionalization of Imidazo[1, 2‐ a ]pyridine. ChemistrySelect 2021;6:2716-44. [DOI: 10.1002/slct.202100144] [Cited by in Crossref: 4] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]
15 Ma C, Chen M, Feng Z, Zhang Y, Wang J, Jiang Y, Yu B. Functionalization of imidazo[1,2- a ]pyridines via radical reactions. New J Chem 2021;45:9302-14. [DOI: 10.1039/d1nj00704a] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
16 Liu S, Jiang H, Liu W, Zhu X, Hao XQ, Song MP. Ruthenium-Catalyzed C(sp2)-H Bond Bisallylation with Imidazopyridines as Directing Groups. J Org Chem 2020;85:15167-82. [PMID: 33140953 DOI: 10.1021/acs.joc.0c02029] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
17 Vuillermet F, Bourret J, Pelletier G. Synthesis of Imidazo[1,2- a ]pyridines: Triflic Anhydride-Mediated Annulation of 2 H -Azirines with 2-Chloropyridines. J Org Chem 2021;86:388-402. [DOI: 10.1021/acs.joc.0c02148] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 2.5] [Reference Citation Analysis]
18 Gao F, Sun K, Chen XL, Shi T, Li XY, Qu LB, Zhao YF, Yu B. Visible-Light-Induced Phosphorylation of Imidazo-Fused Heterocycles under Metal-Free Conditions. J Org Chem 2020;85:14744-52. [PMID: 33136392 DOI: 10.1021/acs.joc.0c02107] [Cited by in Crossref: 10] [Cited by in F6Publishing: 7] [Article Influence: 5.0] [Reference Citation Analysis]
19 Wang Y, Li J, Wang X, Shi L, Zhu X, Hao X, Song M. Rh(III)-catalyzed C–H acylmethylation of 2H-indazoles with sulfoxonium ylides. Journal of Saudi Chemical Society 2020;24:850-6. [DOI: 10.1016/j.jscs.2020.09.001] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
20 Li J, Shi L, Zhang SP, Wang XY, Zhu X, Hao XQ, Song MP. Rh(III)-Catalyzed C-H Cyanation of 2H-Indazole with N-Cyano-N-phenyl-p-toluenesulfonamide. J Org Chem 2020;85:10835-45. [PMID: 32692175 DOI: 10.1021/acs.joc.0c01386] [Cited by in Crossref: 13] [Cited by in F6Publishing: 4] [Article Influence: 6.5] [Reference Citation Analysis]
21 Zhu Y, Xue Y, Liu W, Zhu X, Hao X, Song M. Temperature-Controlled Chalcogenation and Chalcogenocyanation of Imidazopyridines in Water under Transition Metal-Free Conditions. J Org Chem 2020;85:9106-16. [DOI: 10.1021/acs.joc.0c01035] [Cited by in Crossref: 17] [Cited by in F6Publishing: 7] [Article Influence: 8.5] [Reference Citation Analysis]
22 Park JW, Kim YH, Kim DY. Electrochemical oxidative iodination of imidazo[1,2- a ]pyridines using NaI as iodine source. Synthetic Communications 2020;50:710-8. [DOI: 10.1080/00397911.2020.1717539] [Cited by in Crossref: 11] [Cited by in F6Publishing: 3] [Article Influence: 5.5] [Reference Citation Analysis]
23 Shi T, Sun K, Chen X, Zhang Z, Huang X, Peng Y, Qu L, Yu B. Recyclable Perovskite as Heterogeneous Photocatalyst for Aminomethylation of Imidazo‐Fused Heterocycles. Adv Synth Catal 2020;362:2143-9. [DOI: 10.1002/adsc.201901324] [Cited by in Crossref: 28] [Cited by in F6Publishing: 37] [Article Influence: 14.0] [Reference Citation Analysis]
24 Tashrifi Z, Mohammadi-khanaposhtani M, Larijani B, Mahdavi M. C3-Functionalization of Imidazo[1,2- a ]pyridines: C3-Functionalization of Imidazo[1,2- a ]pyridines. Eur J Org Chem 2020;2020:269-84. [DOI: 10.1002/ejoc.201901491] [Cited by in Crossref: 39] [Cited by in F6Publishing: 11] [Article Influence: 19.5] [Reference Citation Analysis]
25 Wen J, Niu C, Yan K, Cheng X, Gong R, Li M, Guo Y, Yang J, Wang H. Electrochemical-induced regioselective C-3 thiomethylation of imidazopyridines via a three-component cross-coupling strategy. Green Chem 2020;22:1129-33. [DOI: 10.1039/c9gc04068d] [Cited by in Crossref: 22] [Article Influence: 11.0] [Reference Citation Analysis]
26 Li B, Shen N, Yang Y, Zhang X, Fan X. Synthesis of naphtho[1′,2′:4,5]imidazo[1,2- a ]pyridines via Rh( iii )-catalyzed C–H functionalization of 2-arylimidazo[1,2- a ]pyridines with cyclic 2-diazo-1,3-diketones featuring with a ring opening and reannulation. Org Chem Front 2020;7:919-25. [DOI: 10.1039/d0qo00073f] [Cited by in Crossref: 11] [Article Influence: 5.5] [Reference Citation Analysis]
27 Wang Q, Shi L, Liu S, Zhi C, Fu L, Zhu X, Hao X, Song M. Solvent-free and room temperature microwave-assisted direct C7 allylation of indolines via sequential C–H and C–C activation. RSC Adv 2020;10:10883-7. [DOI: 10.1039/d0ra02016h] [Cited by in Crossref: 5] [Article Influence: 2.5] [Reference Citation Analysis]
28 Zhi C, Wang Q, Liu S, Xue Y, Shi L, Zhu X, Hao X, Song M. Cu-Catalyzed Direct C7 Sulfonylation of Indolines with Arylsulfonyl Chlorides. J Org Chem 2020;85:1022-32. [DOI: 10.1021/acs.joc.9b02954] [Cited by in Crossref: 15] [Cited by in F6Publishing: 10] [Article Influence: 5.0] [Reference Citation Analysis]
29 Mi X, Kong Y, Zhang J, Pi C, Cui X. Visible-light-promoted sulfonylmethylation of imidazopyridines. Chinese Chemical Letters 2019;30:2295-8. [DOI: 10.1016/j.cclet.2019.09.040] [Cited by in Crossref: 27] [Cited by in F6Publishing: 12] [Article Influence: 9.0] [Reference Citation Analysis]
30 Sandeep M, Muzaffar-ur-rehman M, Pradeep Kumar G, Sridhar B, Reddy KR. One-Pot Synthesis of 3-Sulfenyl/Selenylimidazo[1,5- a ]quinolines from 2-Methylquinolines, Aliphatic Amines/Amino Acids, and Dichalcogenides: One-Pot Synthesis of 3-Sulfenyl/Selenylimidazo[1,5- a ]quinolines from 2-Methylquinolines, Aliphatic Amines/Amino Acids, and Dichalcogenides. Eur J Org Chem 2019;2019:6122-31. [DOI: 10.1002/ejoc.201901174] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]