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For: Matsuo K, Yamaguchi E, Itoh A. In Situ-Generated Halogen-Bonding Complex Enables Atom Transfer Radical Addition (ATRA) Reactions of Olefins. J Org Chem 2020;85:10574-83. [DOI: 10.1021/acs.joc.0c01135] [Cited by in Crossref: 11] [Cited by in F6Publishing: 4] [Article Influence: 5.5] [Reference Citation Analysis]
Number Citing Articles
1 Matsuo K, Yoshitake T, Yamaguchi E, Itoh A. Photoinduced Atom Transfer Radical Addition/Cyclization Reaction between Alkynes or Alkenes with Unsaturated α-Halogenated Carbonyls. Molecules 2021;26:6781. [PMID: 34833874 DOI: 10.3390/molecules26226781] [Reference Citation Analysis]
2 Bianchi P, Williams JD, Kappe CO. Continuous flow processing of bismuth-photocatalyzed atom transfer radical addition reactions using an oscillatory flow reactor. Green Chem 2021;23:2685-93. [DOI: 10.1039/d0gc03070h] [Cited by in Crossref: 10] [Cited by in F6Publishing: 4] [Article Influence: 10.0] [Reference Citation Analysis]
3 Liautard V, Delgado M, Colin B, Chabaud L, Michaud G, Pucheault M. In situ generation of radical initiators using amine-borane complexes for carbohalogenation of alkenes. Chem Commun . [DOI: 10.1039/d1cc06390a] [Reference Citation Analysis]
4 Tasnim T, Ryan C, Christensen ML, Fennell CJ, Pitre SP. Radical Perfluoroalkylation Enabled by a Catalytically Generated Halogen Bonding Complex and Visible Light Irradiation. Org Lett 2021. [PMID: 34914870 DOI: 10.1021/acs.orglett.1c04139] [Reference Citation Analysis]
5 Li JZ, Zhang WK, Ge GP, Zheng H, Wei WT. Recent progress in the radical α-C(sp3)-H functionalization of ketones. Org Biomol Chem 2021;19:7333-47. [PMID: 34612358 DOI: 10.1039/d1ob01408k] [Reference Citation Analysis]
6 Zheng L, Cai L, Tao K, Xie Z, Lai Y, Guo W. Progress in Photoinduced Radical Reactions using Electron Donor‐Acceptor Complexes. Asian J Org Chem 2021;10:711-48. [DOI: 10.1002/ajoc.202100009] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 6.0] [Reference Citation Analysis]
7 Wu C, Hui X, Zhang D, Zhang M, Zhu Y, Wang S. Visible light-mediated polychlorination of alkenes via the dichloromethyl radical generated by chloroform and chlorides. Green Chem . [DOI: 10.1039/d1gc04109f] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
8 Zeng X, Xu Y, Liu J, Deng Y. Access to gem-Dibromoenones Enabled by Carbon-Centered Radical Addition to Terminal Alkynes in Water Solution. Org Lett 2021;23:9058-62. [PMID: 34766780 DOI: 10.1021/acs.orglett.1c03305] [Reference Citation Analysis]
9 Steiner A, de Frutos O, Rincón JA, Mateos C, Williams JD, Kappe CO. N -Chloroamines as substrates for metal-free photochemical atom-transfer radical addition reactions in continuous flow. React Chem Eng 2021;6:2434-41. [DOI: 10.1039/d1re00429h] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
10 Wang Y, Tu K, Cheng J, He E, Wang J, Zhang L, Cheng Z. Facile photochemical synthesis of main-chain-type semifluorinated alternating copolymers catalyzed by conventional amines or halide salts. Chem Commun (Camb) 2021;57:11354-7. [PMID: 34643625 DOI: 10.1039/d1cc04967d] [Reference Citation Analysis]
11 Kato N, Nanjo T, Takemoto Y. A Pyridine-Based Donor–Acceptor Molecule: A Highly Reactive Organophotocatalyst That Enables the Reductive Cleavage of C–Br Bonds through Halogen Bonding. ACS Catal . [DOI: 10.1021/acscatal.2c02067] [Reference Citation Analysis]
12 Worp BA, Kosobokov MD, Dilman AD. Visible‐Light‐Promoted Reversible Sulfide/Iodide Exchange in Fluoroalkyl Sulfides Enabled by Electron Donor‐Acceptor Complex Formation. ChemPhotoChem 2021;5:565-70. [DOI: 10.1002/cptc.202100042] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
13 Barata-vallejo S, Yerien DE, Postigo A. Advances in Photocatalytic Organic Synthetic Transformations in Water and Aqueous Media. ACS Sustainable Chem Eng 2021;9:10016-47. [DOI: 10.1021/acssuschemeng.1c03384] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]