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Cited by in F6Publishing
For: Kishi A, Moriyama K, Togo H. Preparation of Phenanthridines from o -Cyanobiaryls via Addition of Organic Lithiums to Nitriles and Imino Radical Cyclization with Iodine. J Org Chem 2018;83:11080-8. [DOI: 10.1021/acs.joc.8b01688] [Cited by in Crossref: 23] [Cited by in F6Publishing: 22] [Article Influence: 5.8] [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 Hess A, Guelen HC, Alandini N, Mourati A, Guersoy YC, Knochel P. Preparation of Polyfunctionalized Aromatic Nitriles from Aryl Oxazolines. Chemistry 2021. [PMID: 34766655 DOI: 10.1002/chem.202103700] [Cited by in F6Publishing: 2] [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 Xu Y, Yu C, Zhang X, Fan X. Selective Synthesis of Dihydrophenanthridine and Phenanthridine Derivatives from the Cascade Reactions of o-Arylanilines with Alkynoates through C-H/N-H/C-C Bond Cleavage. J Org Chem 2021;86:5805-19. [PMID: 33793223 DOI: 10.1021/acs.joc.1c00256] [Cited by in Crossref: 4] [Cited by in F6Publishing: 6] [Article Influence: 4.0] [Reference Citation Analysis]
5 Kaur M, Garg S, Malhi DS, Sohal HS. A Review on Synthesis, Reactions and Biological Properties of Seven Membered Heterocyclic Compounds: Azepine, Azepane, Azepinone. COC 2021;25:449-506. [DOI: 10.2174/1385272825999210104222338] [Cited by in Crossref: 4] [Cited by in F6Publishing: 7] [Article Influence: 4.0] [Reference Citation Analysis]
6 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]
7 Talukdar V, Vijayan A, Kumar Katari N, Radhakrishnan KV, Das P. Recent Trends in the Synthesis and Mechanistic Implications of Phenanthridines. Adv Synth Catal 2021;363:1202-45. [DOI: 10.1002/adsc.202001236] [Cited by in Crossref: 4] [Cited by in F6Publishing: 6] [Article Influence: 4.0] [Reference Citation Analysis]
8 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: 4] [Article Influence: 3.0] [Reference Citation Analysis]
9 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: 8] [Article Influence: 4.0] [Reference Citation Analysis]
10 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]
11 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]
12 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] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
13 Sako M, Losa R, Takiishi T, Vo-thanh G, Takizawa S, Sasai H. Vanadium(V) Complex-Catalyzed One-Pot Synthesis of Phenanthridines via a Pictet-Spengler-Dehydrogenative Aromatization Sequence. Catalysts 2020;10:860. [DOI: 10.3390/catal10080860] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
14 Zhao M, Barrado AG, Sprenger K, Golz C, Mata RA, Alcarazo M. Electrophilic Cyanative Alkenylation of Arenes. Org Lett 2020;22:4932-7. [PMID: 32432882 DOI: 10.1021/acs.orglett.0c01204] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 2.5] [Reference Citation Analysis]
15 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]
16 Fang B, Hou J, Tian J, Yu W, Chang J. Synthesis of phenanthridines by I 2 -mediated sp 3 C–H amination. Org Biomol Chem 2020;18:3312-23. [DOI: 10.1039/d0ob00433b] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 4.5] [Reference Citation Analysis]
17 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]
18 Uchida K, Togo H. Transformation of aromatic bromides into aromatic nitriles with n-BuLi, pivalonitrile, and iodine under metal cyanide-free conditions. Tetrahedron 2019;75:130550. [DOI: 10.1016/j.tet.2019.130550] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
19 Yao X, Shao Y, Hu M, Xia Y, Cheng T, Chen J. Palladium-Catalyzed Cascade Reaction of o -Cyanobiaryls with Arylboronic Acids: Synthesis of 5-Arylidene-7-aryl-5 H -dibenzo[ c , e ]azepines. Org Lett 2019;21:7697-701. [DOI: 10.1021/acs.orglett.9b02351] [Cited by in Crossref: 23] [Cited by in F6Publishing: 26] [Article Influence: 7.7] [Reference Citation Analysis]
20 He D, Zhuang Z, Wang X, Li J, Li J, Wu W, Zhao Z, Jiang H, Tang BZ. Assembly of 1H-isoindole derivatives by selective carbon-nitrogen triple bond activation: access to aggregation-induced emission fluorophores for lipid droplet imaging. Chem Sci 2019;10:7076-81. [PMID: 31588275 DOI: 10.1039/c9sc01035a] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 3.3] [Reference Citation Analysis]
21 Zhu M, Fu W, Guo W, Tian Y, Wang Z, Ji B. Visible-light-induced radical trifluoromethylthiolation of N-(o-cyanobiaryl)acrylamides. Org Biomol Chem 2019;17:3374-80. [PMID: 30860236 DOI: 10.1039/c9ob00342h] [Cited by in Crossref: 16] [Cited by in F6Publishing: 15] [Article Influence: 5.3] [Reference Citation Analysis]
22 Naruto H, Togo H. Preparation of 2-arylquinolines from β-arylpropionitriles with aryllithiums and NIS through iminyl radical-mediated cyclization. Org Biomol Chem 2019;17:5760-70. [DOI: 10.1039/c9ob00944b] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 3.3] [Reference Citation Analysis]