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For: Cioffi CL, Lansing JJ, Yüksel H. Synthesis of 2-Aminobenzoxazoles Using Tetramethyl Orthocarbonate or 1,1-Dichlorodiphenoxymethane. J Org Chem 2010;75:7942-5. [DOI: 10.1021/jo1017052] [Cited by in Crossref: 25] [Cited by in F6Publishing: 18] [Article Influence: 2.1] [Reference Citation Analysis]
Number Citing Articles
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8 Lv Z, Wang H, Quan Z, Gao Y, Lei A. Dioxygen-triggered oxidative cleavage of the C-S bond towards C-N bond formation. Chem Commun (Camb) 2019;55:12332-5. [PMID: 31556432 DOI: 10.1039/c9cc05707b] [Cited by in Crossref: 2] [Article Influence: 0.7] [Reference Citation Analysis]
9 Aksenov NA, Aksenov AV, Nadein ON, Aksenov DA, Smirnov AN, Rubin M. One-pot synthesis of benzoxazoles via the metal-free ortho-C–H functionalization of phenols with nitroalkanes. RSC Adv 2015;5:71620-6. [DOI: 10.1039/c5ra15128g] [Cited by in Crossref: 32] [Article Influence: 4.6] [Reference Citation Analysis]
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11 Li Y, Xie Y, Zhang R, Jin K, Wang X, Duan C. Copper-Catalyzed Direct Oxidative C–H Amination of Benzoxazoles with Formamides or Secondary Amines under Mild Conditions. J Org Chem 2011;76:5444-9. [DOI: 10.1021/jo200447x] [Cited by in Crossref: 124] [Cited by in F6Publishing: 99] [Article Influence: 11.3] [Reference Citation Analysis]
12 Lin C, Hsieh T, Liao P, Liao Z, Chang C, Shih Y, Yeh W, Chien T. Practical Synthesis of N -Substituted Cyanamides via Tiemann Rearrangement of Amidoximes. Org Lett 2014;16:892-5. [DOI: 10.1021/ol403645y] [Cited by in Crossref: 45] [Cited by in F6Publishing: 29] [Article Influence: 5.6] [Reference Citation Analysis]
13 Keshari T, Srivastava VP, Yadav LDS. Visible-light-initiated photo-oxidative cyclization of phenolic amidines using CBr4 – A metal free approach to 2-aminobenzoxazoles. RSC Adv 2014;4:5815. [DOI: 10.1039/c3ra46314a] [Cited by in Crossref: 16] [Cited by in F6Publishing: 13] [Article Influence: 2.0] [Reference Citation Analysis]
14 Lester RP, Bham T, Bousfield TW, Lewis W, Camp JE. Exploring the Reactivity of 2-Trichloromethylbenzoxazoles for Access to Substituted Benzoxazoles. J Org Chem 2016;81:12472-7. [DOI: 10.1021/acs.joc.6b02315] [Cited by in Crossref: 10] [Cited by in F6Publishing: 8] [Article Influence: 1.7] [Reference Citation Analysis]
15 Lamani M, Prabhu KR. Iodine-Catalyzed Amination of Benzoxazoles: A Metal-Free Route to 2-Aminobenzoxazoles under Mild Conditions. J Org Chem 2011;76:7938-44. [DOI: 10.1021/jo201402a] [Cited by in Crossref: 115] [Cited by in F6Publishing: 82] [Article Influence: 10.5] [Reference Citation Analysis]
16 Pattarawarapan M, Wiriya N, Yimklan S, Wangngae S, Phakhodee W. Zwitterionic Ring-Opened Oxyphosphonium Species from the Ph3P-I2 Mediated Reactions of Benzo[d]oxazol-2(3H)-ones with Secondary Amines. J Org Chem 2020;85:6151-8. [PMID: 32242407 DOI: 10.1021/acs.joc.0c00211] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
17 Rapolu T, Naveen P, Pavan Kumar K, Reddy Leleti K, korapolu R. Microwave assisted one pot synthesis of 2-alkyl amino benzimidazoles, 2-alkyl amino benzoxazoles and 2-alkyl amino benzthiazoles by using various carbodiimides. Results in Chemistry 2022. [DOI: 10.1016/j.rechem.2022.100351] [Reference Citation Analysis]
18 Bhujabal YB, Vadagaonkar KS, Gholap A, Sanghvi YS, Dandela R, Kapdi AR. HFIP Promoted Low-Temperature S N Ar of Chloroheteroarenes Using Thiols and Amines. J Org Chem 2019;84:15343-54. [DOI: 10.1021/acs.joc.9b02371] [Cited by in Crossref: 10] [Cited by in F6Publishing: 5] [Article Influence: 3.3] [Reference Citation Analysis]
19 Šlachtová V, Chasák J, Brulíková L. Synthesis of Various 2-Aminobenzoxazoles: The Study of Cyclization and Smiles Rearrangement. ACS Omega 2019;4:19314-23. [PMID: 31763555 DOI: 10.1021/acsomega.9b02702] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.7] [Reference Citation Analysis]
20 Yotphan S, Beukeaw D, Reutrakul V. Synthesis of 2-aminobenzoxazoles via copper-catalyzed electrophilic amination of benzoxazoles with O-benzoyl hydroxylamines. Tetrahedron 2013;69:6627-33. [DOI: 10.1016/j.tet.2013.05.127] [Cited by in Crossref: 28] [Cited by in F6Publishing: 13] [Article Influence: 3.1] [Reference Citation Analysis]