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For: Schotten C, Leprevost SK, Yong LM, Hughes CE, Harris KDM, Browne DL. Comparison of the Thermal Stabilities of Diazonium Salts and Their Corresponding Triazenes. Org Process Res Dev 2020;24:2336-41. [DOI: 10.1021/acs.oprd.0c00162] [Cited by in Crossref: 9] [Cited by in F6Publishing: 15] [Article Influence: 4.5] [Reference Citation Analysis]
Number Citing Articles
1 Venkatesh R, Tiwari V, Kandasamy J. Copper(I)-Catalyzed Sandmeyer-Type S-Arylation of 1-Thiosugars with Aryldiazonium Salts under Mild Conditions. J Org Chem 2022. [PMID: 35994736 DOI: 10.1021/acs.joc.2c00930] [Reference Citation Analysis]
2 Katagiri K, Kuriyama M, Yamamoto K, Demizu Y, Onomura O. Organocatalytic Synthesis of Phenols from Diaryliodonium Salts with Water under Metal-Free Conditions. Org Lett 2022. [PMID: 35822911 DOI: 10.1021/acs.orglett.2c01989] [Reference Citation Analysis]
3 Guo D, Shi W, Zou G. Suzuki Coupling of Activated Aryltriazenes for Practical Synthesis of Biaryls from Anilines. Adv Synth Catal. [DOI: 10.1002/adsc.202200433] [Reference Citation Analysis]
4 Prabhala P, Sutar SM, Kalkhambkar RG, Jeong YT. Ultrasonication Assisted α‐Arylation of N‐ heteroarenes Employing 1‐Aryltriazenes Promoted by Brønsted Acidic Ionic Liquid under Aerobic Conditions. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202201428] [Reference Citation Analysis]
5 Herrera CL, Santiago JV, Pastre JC, Correia CRD. In Tandem Auto‐Sustainable Enantioselective Heck‐Matsuda Reactions Directly from Anilines. Adv Synth Catal 2022;364:1863-72. [DOI: 10.1002/adsc.202200205] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Vargas DF, Kaufman TS, Larghi EL. Total Synthesis of Aqabamycin G, a Nitrophenyl Indolylmaleimide Marine Alkaloid from Vibrio sp. WMBA. J Org Chem 2022. [PMID: 35324169 DOI: 10.1021/acs.joc.2c00063] [Reference Citation Analysis]
7 Xie C, Yuan Y, Wang B, Du L. Research on the decomposition kinetics and thermal hazards of aniline diazonium salt. Thermochimica Acta 2022;709:179156. [DOI: 10.1016/j.tca.2022.179156] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Schäfer G, Fleischer T, Blumer N, Udry M, Reber S, Stansfield I, Liu Y, Li Y, Li P. Initial Route Scouting and Final Process Development for the Multi-Kg Production of 3-Fluoro-6-methoxyquinoline from p -Anisidine and 2-Fluoromalonic Acid. Org Process Res Dev . [DOI: 10.1021/acs.oprd.1c00414] [Reference Citation Analysis]
9 Ito M, Yamabayashi Y, Takishima Y, Higuchi K, Sugiyama S. Aryne Generation from <i>o</i>-Triazenylarylboronic Acids Induced by Brønsted Acid. Chem Pharm Bull . [DOI: 10.1248/cpb.c22-00264] [Reference Citation Analysis]
10 Chen J, Xie X, Liu J, Yu Z, Su W. Revisiting aromatic diazotization and aryl diazonium salts in continuous flow: highlighted research during 2001–2021. React Chem Eng 2022;7:1247-75. [DOI: 10.1039/d2re00001f] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Davis GJ, Townsend JA, Morrow MG, Hamie M, Shepard AJ, Hsieh CC, Marty MT, Jewett JC. Protein Modification via Mild Photochemical Isomerization of Triazenes to Release Aryl Diazonium Ions. Bioconjug Chem 2021;32:2432-8. [PMID: 34730351 DOI: 10.1021/acs.bioconjchem.1c00459] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
12 Lu GH, Huang TC, Hsueh HC, Yang SC, Cho TW, Chou HH. Novel N-transfer reagent for converting α-amino acid derivatives to α-diazo compounds. Chem Commun (Camb) 2021;57:4839-42. [PMID: 33870368 DOI: 10.1039/d1cc01285a] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
13 Abrams J. Alternative method for the synthesis of triazenes from aryl diazonium salts. Tetrahedron 2021;89:132185. [DOI: 10.1016/j.tet.2021.132185] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
14 Ito M, Yamabayashi Y, Oikawa M, Kano E, Higuchi K, Sugiyama S. Silica gel-induced aryne generation from o -triazenylarylboronic acids as stable solid precursors. Org Chem Front 2021;8:2963-9. [DOI: 10.1039/d1qo00385b] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
15 Suleymanov AA, Severin K. Vinyl and Alkynyl Triazenes: Synthesis, Reactivity, and Applications. Angew Chem Int Ed Engl 2021;60:6879-89. [PMID: 33142011 DOI: 10.1002/anie.202011031] [Cited by in Crossref: 4] [Cited by in F6Publishing: 9] [Article Influence: 2.0] [Reference Citation Analysis]