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For: Cots E, Flores A, Romero RM, Muñiz K. A Practical Aryliodine(I/III) Catalysis for the Vicinal Diamination of Styrenes. ChemSusChem 2019;12:3028-31. [PMID: 30803150 DOI: 10.1002/cssc.201900360] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
Number Citing Articles
1 Fan Z, Wang Z, Shi R, Wang Y. Dirhodium( ii )-catalyzed diamination reaction via a free radical pathway. Org Chem Front 2021;8:5098-104. [DOI: 10.1039/d1qo00894c] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
2 Malviya BK, Jassal AK, Karnatak M, Verma VP, Sharma S. Electro-Oxidative sp3 C-H Bond Functionalization and Annulation Cascade: Synthesis of Novel Heterocyclic Substituted Indolizines. J Org Chem 2022. [PMID: 35104140 DOI: 10.1021/acs.joc.1c02773] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
3 Li HH, Li JQ, Zheng X, Huang PQ. Photoredox-Catalyzed Decarboxylative Cross-Coupling of α-Amino Acids with Nitrones. Org Lett 2021;23:876-80. [PMID: 33433222 DOI: 10.1021/acs.orglett.0c04101] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 5.0] [Reference Citation Analysis]
4 Wang D, Yu H, Sun S, Zhong F. Intermolecular Vicinal Diaminative Assembly of Tetrahydroquinoxalines via Metal-free Oxidative [4 + 2] Cycloaddition Strategy. Org Lett 2020;22:2425-30. [DOI: 10.1021/acs.orglett.0c00624] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 3.5] [Reference Citation Analysis]
5 Cots E, Rintjema J, Bravo F, Muñiz K. Deciphering the Keys for High Enantioselectivity in Hypervalent Iodine-Catalyzed 1,2-Difunctionalization: Improved Synthesis of Ishihara-Muñiz Precatalysts. Org Lett 2021;23:6429-34. [PMID: 34346687 DOI: 10.1021/acs.orglett.1c02252] [Reference Citation Analysis]
6 Bal A, Maiti S, Mal P. Strategies to Control Hypervalent Iodine – Primary Amine Reactions. Chem Asian J 2020;15:624-35. [DOI: 10.1002/asia.201901683] [Cited by in Crossref: 7] [Cited by in F6Publishing: 3] [Article Influence: 3.5] [Reference Citation Analysis]
7 Deng XJ, Liu HX, Zhang LW, Zhang GY, Yu ZX, He W. Iodoarene-Catalyzed Oxyamination of Unactivated Alkenes to Synthesize 5-Imino-2-Tetrahydrofuranyl Methanamine Derivatives. J Org Chem 2021;86:235-53. [PMID: 33336571 DOI: 10.1021/acs.joc.0c02047] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
8 Bai X, Huang L, Zhou P, Xi H, Hu J, Zuo Z, Feng H. Selectivity Controlled Hydroamination of Alkynes to Sulfonyl Fluoride Hubs: Development and Application. J Org Chem 2022. [PMID: 35316042 DOI: 10.1021/acs.joc.1c03082] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Dong M, Wang D, Tong X. PhI(OAc)2-Mediated Dihalogenative Cyclization of 1,6-Enyne with Lithium Halide. Org Lett 2021;23:3588-92. [PMID: 33899488 DOI: 10.1021/acs.orglett.1c00987] [Reference Citation Analysis]
10 Kimura T, Hamada S, Furuta T, Takemoto Y, Kobayashi Y. N-Acylimino-λ3-iodanes from the Metathesis of Iodosoarenes and Nitriles for the Photoinduced C-H Perfluoroacylamination of (Hetero)Arenes. Org Lett 2022. [PMID: 35758853 DOI: 10.1021/acs.orglett.2c02054] [Reference Citation Analysis]
11 Kobayashi Y, Masakado S, Murai T, Hamada S, Furuta T, Takemoto Y. A bench-stable N-trifluoroacetyl nitrene equivalent for a simple synthesis of 2-trifluoromethyl oxazoles. Org Biomol Chem 2021;19:6628-32. [PMID: 34282812 DOI: 10.1039/d1ob00947h] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Li X, Li G, Cheng Y, Du Y. The aryl iodine-catalyzed organic transformation via hypervalent iodine species generated in situ. Physical Sciences Reviews 2022;0:000010151520210019. [DOI: 10.1515/psr-2021-0019] [Reference Citation Analysis]
13 Caspers LD, Spils J, Damrath M, Lork E, Nachtsheim BJ. One-Pot Synthesis and Conformational Analysis of Six-Membered Cyclic Iodonium Salts. J Org Chem 2020;85:9161-78. [PMID: 32539390 DOI: 10.1021/acs.joc.0c01125] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]