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Cited by in F6Publishing
For: Kobayashi E, Kishi A, Togo H. 6-Arylphenanthridines from Aryl o -Biaryl Ketones with 1,1,1,3,3,3-Hexamethyldisilazane and Molecular Iodine: 6-Arylphenanthridines from Aryl o -Biaryl Ketones with 1,1,1,3,3,3-Hexamethyldisilazane and Molecular Iodine. Eur J Org Chem 2019;2019:7335-47. [DOI: 10.1002/ejoc.201901278] [Cited by in Crossref: 12] [Cited by in F6Publishing: 11] [Article Influence: 4.0] [Reference Citation Analysis]
Number Citing Articles
1 Nakamura M, Yoshida K, Togo H. Novel preparation of 2,5-diarylpyrroles from aromatic nitriles with 3-arylpropylmagnesium bromides, 1,3-diiodo-5,5-dimethylhydantoin, and BuOK. Tetrahedron 2022. [DOI: 10.1016/j.tet.2022.132709] [Reference Citation Analysis]
2 Kuciński K, Stachowiak H, Lewandowski D, Gruszczyński M, Lampasiak P, Hreczycho G. A review of the R3Si–NH–SiR3–type disilazanes: From synthesis to applications. Journal of Organometallic Chemistry 2022;961:122127. [DOI: 10.1016/j.jorganchem.2021.122127] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
3 Gao Y, Zhao Q, Li L, Ma YN. Synthesis of Six-Membered N-Heterocycle Frameworks Based on Intramolecular Metal-Free N-Centered Radical Chemistry. Chem Rec 2021. [PMID: 34618405 DOI: 10.1002/tcr.202100218] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
4 Naruto H, Togo H. Facile preparation of 3-aryl-4-iodoisoquinolines from N-(o-Arylethynyl)benzyl p-toluenesulfonamides with iodine and base. Tetrahedron 2021;83:131993. [DOI: 10.1016/j.tet.2021.131993] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
5 Yanai K, Togo H. Preparation of phenanthridines from N-(o-arylbenzyl)trifluoromethanesulfonamides with 1,3-diiodo-5,5-dimethylhydantoin. Tetrahedron 2020;76:131503. [DOI: 10.1016/j.tet.2020.131503] [Cited by in Crossref: 6] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
6 Gao Y, Jing Y, Li L, Zhang J, Chen X, Ma Y. Synthesis of Phenanthridines through Iodine-Supported Intramolecular C–H Amination and Oxidation under Visible Light. J Org Chem 2020;85:12187-98. [DOI: 10.1021/acs.joc.0c01390] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
7 Zhang Y, Zhang D, Wei J, Hong X, Lu Y, Hu D, Li G, Liu Z, Chen Y, Duan L. Achieving Pure Green Electroluminescence with CIEy of 0.69 and EQE of 28.2% from an Aza‐Fused Multi‐Resonance Emitter. Angew Chem 2020;132:17652-6. [DOI: 10.1002/ange.202008264] [Cited by in Crossref: 23] [Cited by in F6Publishing: 35] [Article Influence: 11.5] [Reference Citation Analysis]
8 Zhang Y, Zhang D, Wei J, Hong X, Lu Y, Hu D, Li G, Liu Z, Chen Y, Duan L. Achieving Pure Green Electroluminescence with CIEy of 0.69 and EQE of 28.2% from an Aza‐Fused Multi‐Resonance Emitter. Angew Chem Int Ed 2020;59:17499-503. [DOI: 10.1002/anie.202008264] [Cited by in Crossref: 31] [Cited by in F6Publishing: 83] [Article Influence: 15.5] [Reference Citation Analysis]
9 Naruto H, Togo H. Preparation of 4-arylquinazolines with o-(N-alkyl,N-p-tosyl)aminobenzonitriles, aryllithiums, and NIS. Org Biomol Chem 2020;18:5666-76. [PMID: 32662475 DOI: 10.1039/d0ob01223h] [Cited by in Crossref: 3] [Article Influence: 1.5] [Reference Citation Analysis]
10 Saito A, Togo H. Photochemical Transformation of O -(β-Arylethyl) Arylimidates into 2,4-Diaryl-5-iodoxazoles with 1,3-Diiodo-5,5-dimethylhydantoin: Photochemical Transformation of O -(β-Arylethyl) Arylimidates into 2,4-Diaryl-5-iodoxazoles with 1,3-Diiodo-5,5-dimethylhydantoin. Eur J Org Chem 2020;2020:3320-31. [DOI: 10.1002/ejoc.202000383] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
11 Teslenko FE, Churakov AI, Larin AA, Ananyev IV, Fershtat LL, Makhova NN. Route to 1,2,4- and 1,2,5-oxadiazole ring assemblies via a one-pot condensation/oxidation protocol. Tetrahedron Letters 2020;61:151678. [DOI: 10.1016/j.tetlet.2020.151678] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]