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For: Durka J, Turkowska J, Gryko D. Lightening Diazo Compounds? ACS Sustainable Chem Eng 2021;9:8895-918. [DOI: 10.1021/acssuschemeng.1c01976] [Cited by in Crossref: 43] [Cited by in F6Publishing: 47] [Article Influence: 43.0] [Reference Citation Analysis]
Number Citing Articles
1 Li Z, Yao X, Zhang X, Mei H, Han J. Carboxylic Acid O–H Insertion Reaction of β-Ester Diazos Enabling Synthesis of β-Acyloxy Esters. J Org Chem 2022. [DOI: 10.1021/acs.joc.2c02023] [Reference Citation Analysis]
2 Wang H, Wang S, George V, Llorente G, König B. Photo‐Induced Homologation of Carbonyl Compounds for Iterative Syntheses. Angew Chem Int Ed 2022. [DOI: 10.1002/anie.202211578] [Reference Citation Analysis]
3 Davas DS, Gopalakrishnan DK, Kumar D, Vaitla J. Ru-Catalyzed Benzannulation of Vinyl Sulfoxonium Ylide with Electron-Deficient Alkynes and Alkenes. Org Lett 2022. [DOI: 10.1021/acs.orglett.2c03388] [Reference Citation Analysis]
4 Wang Q, Liu J, Mei H, Pajkert R, Kessler M, Röschenthaler G, Han J. Ru-Catalyzed Hydrogen Atom Transfer/C–F Bond Cleavage of Difluoroalkyl Diazos with Hantzsch Ester via a Photocatalytic Radical Process. Org Lett 2022. [DOI: 10.1021/acs.orglett.2c03268] [Reference Citation Analysis]
5 Wang J. Diazo compounds: Recent applications in synthetic organic chemistry and beyond. Tetrahedron Letters 2022;108:154135. [DOI: 10.1016/j.tetlet.2022.154135] [Reference Citation Analysis]
6 Li W, Yang Y, Tang Z, Yu X, Lin J, Jin Y. Visible-Light-Promoted Carbene Insertion and Decarbonylation for the Synthesis of α-Substituted γ-Ketoesters. J Org Chem 2022. [PMID: 36130043 DOI: 10.1021/acs.joc.2c01552] [Reference Citation Analysis]
7 Liu Y, Zhu K, Zhao J, Li P. Photocatalytic Regioselective Difunctionalization of Alkenes with Diazo Compounds and tert-Butyl Nitrite: Access to γ-Oximino Esters. Org Lett 2022. [PMID: 36073998 DOI: 10.1021/acs.orglett.2c02749] [Reference Citation Analysis]
8 Cai BG, Yao WZ, Li L, Xuan J. Visible-Light-Induced Imide Synthesis through a Nitrile Ylide Formation/Trapping Cascade. Org Lett 2022. [PMID: 36053175 DOI: 10.1021/acs.orglett.2c02671] [Reference Citation Analysis]
9 Cai B, Li Q, Empel C, Li L, Koenigs RM, Xuan J. Dark and Light Reactions of Carbenes─Merging Carbene Transfer Reactions with N-Heterocyclic Carbene Catalysis for the Synthesis of Hydroxamic Acid Esters. ACS Catal . [DOI: 10.1021/acscatal.2c02875] [Reference Citation Analysis]
10 Zhao S, Gao N, Bao N, Qian M, Chen ZY, Zhang MJ, Chen X. Stereoselective Synthesis of Tetrasubstituted Olefins via Visible-Light-Promoted Iodine-Mediated Homo-Coupling of Diazo. J Org Chem 2022. [PMID: 36001822 DOI: 10.1021/acs.joc.2c01647] [Reference Citation Analysis]
11 Karmakar U, Hwang HS, Lee Y, Cho EJ. Photocatalytic para-Selective C-H Functionalization of Anilines with Diazomalonates. Org Lett 2022. [PMID: 35973228 DOI: 10.1021/acs.orglett.2c02228] [Reference Citation Analysis]
12 Zhu K, Cao M, Zhao G, Zhao J, Li P. Visible Light-Promoted Diazoacetates and Nitriles Generating Nitrilium Ions Trapped by Benzotriazoles and Carboxylic Acids. Org Lett 2022. [PMID: 35916596 DOI: 10.1021/acs.orglett.2c02426] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
13 Wang Y, Jia P, Hao Y, Li J, Lai R, Guo L, Wu Y. Blue light induced [2,3]-sigmatropic rearrangement reactions of tosylhydrazones. Tetrahedron Letters 2022. [DOI: 10.1016/j.tetlet.2022.154098] [Reference Citation Analysis]
14 Langletz T, Empel C, Jana S, Koenigs RM. Stereoconvergent, photocatalytic cyclopropanation reactions of β-substituted styrenes with ethyl diazoacetate. Tetrahedron Chem 2022;3:100024. [DOI: 10.1016/j.tchem.2022.100024] [Reference Citation Analysis]
15 Yang W, Yang Z, Chen L, Lu Y, Zhang C, Su Z, Liu X, Feng X. Chiral nickel(II) complex catalyzed asymmetric [3 + 2] cycloaddition of α-diazo pyrazoleamides with 2-siloxy-1-alkenes. Chinese Chemical Letters 2022. [DOI: 10.1016/j.cclet.2022.107791] [Reference Citation Analysis]
16 Liu GX, Liang HC, Fu X, Tang J, Hu WH, Qiu H. Photoredox-Catalyzed Carbonyl Alkylative Amination with Diazo Compounds: A Three-Component Reaction for the Construction of γ-Amino Acid Derivatives. Org Lett 2022;24:4908-13. [PMID: 35793070 DOI: 10.1021/acs.orglett.2c01751] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
17 Li F, Zhu S, Koenigs RM. Photocatalytic 1,2-oxo-alkylation reaction of styrenes with diazoacetates. Chem Commun (Camb) 2022. [PMID: 35703319 DOI: 10.1039/d2cc02414d] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
18 Phelps R, Orr-Ewing AJ. Direct Observation of the Dynamics of Ylide Solvation by Hydrogen-bond Donors Using Time-Resolved Infrared Spectroscopy. J Am Chem Soc 2022. [PMID: 35580274 DOI: 10.1021/jacs.2c01208] [Reference Citation Analysis]
19 Gallardo GM, Ventura DJ, Petit AS. Computationally Probing the Mechanism of the Blue-Light-Driven O–H Functionalization of Alcohols by Aryldiazoacetates: Photobasicity or Carbene Chemistry. J Org Chem . [DOI: 10.1021/acs.joc.2c00442] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
20 Munaretto LS, Gallo RDC, Leão LPMO, Jurberg ID. H-F bond insertions into α-diazo carbonyl compounds. Org Biomol Chem 2022. [PMID: 35357390 DOI: 10.1039/d2ob00400c] [Reference Citation Analysis]
21 Roy S, Chatterjee I. Visible-Light-Mediated ( sp3 )Cα–H Functionalization of Ethers Enabled by Electron Donor–Acceptor Complex. ACS Org Inorg Au. [DOI: 10.1021/acsorginorgau.2c00008] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
22 He Y, Huang Z, Wu K, Ma J, Zhou YG, Yu Z. Recent advances in transition-metal-catalyzed carbene insertion to C-H bonds. Chem Soc Rev 2022. [PMID: 35297455 DOI: 10.1039/d1cs00895a] [Cited by in Crossref: 25] [Cited by in F6Publishing: 17] [Article Influence: 25.0] [Reference Citation Analysis]
23 Sakharov PA, Novikov MS, Nguyen TK, Kinzhalov MA, Khlebnikov AF, Rostovskii NV. Blue Light-Promoted Cross-Coupling of α-Diazo Esters with Isocyanides: Synthesis of Ester-Functionalized Ketenimines. ACS Omega 2022;7:9071-9. [PMID: 35309460 DOI: 10.1021/acsomega.2c00367] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
24 Chen ZL, Empel C, Wang K, Wu PP, Cai BG, Li L, Koenigs RM, Xuan J. Enabling Cyclopropanation Reactions of Imidazole Heterocycles via Chemoselective Photochemical Carbene Transfer Reactions of NHC-Boranes. Org Lett 2022. [PMID: 35274531 DOI: 10.1021/acs.orglett.2c00609] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
25 Zhou H, Wang G, Wang C, Yang J. Visible-Light-Promoted Aerobic Oxyphosphorylation of α-Diazoesters with H-Phosphine Oxides. Org Lett . [DOI: 10.1021/acs.orglett.2c00198] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
26 Damiano C, Gallo E. Challenging asymmetric alkene cyclopropanation by unsymmetrical diazomalonates. Chem Catalysis 2022;2:229-231. [DOI: 10.1016/j.checat.2022.01.006] [Reference Citation Analysis]
27 Dong S, Liu X, Feng X. Asymmetric Catalytic Rearrangements with α-Diazocarbonyl Compounds. Acc Chem Res 2022;55:415-28. [PMID: 35029358 DOI: 10.1021/acs.accounts.1c00664] [Cited by in Crossref: 32] [Cited by in F6Publishing: 34] [Article Influence: 32.0] [Reference Citation Analysis]
28 Li F, Pei C, Koenigs RM. Photokatalytische gem‐Difluorolefinierungsreaktionen durch eine formale C−C‐Kupplungs/Defluorierungsreaktion mit Diazoacetaten. Angewandte Chemie 2022;134. [DOI: 10.1002/ange.202111892] [Reference Citation Analysis]
29 Bao H, Shi Y, Zhang J, Yang J, Wu J. Stereoselective synthesis of trisubstituted epoxides via cobalt catalysis. Org Chem Front . [DOI: 10.1039/d2qo00815g] [Reference Citation Analysis]
30 Qu C, Liu R, Wang Z, Lv Y, Yue H, Wei W. Visible-light-driven multicomponent reactions to access S -alkyl phosphorothioates using elemental sulfur as the sulfur source. Green Chem 2022;24:4915-20. [DOI: 10.1039/d2gc00903j] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
31 Wang Z, Liu R, Qu C, Zhao X, Lv Y, Yue H, Wei W. Elemental sulfur as the “S” source: visible-light-mediated four-component reactions leading to thiocyanates. Org Chem Front 2022;9:3565-70. [DOI: 10.1039/d2qo00539e] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
32 Ding H, Wang Z, Qu C, Lv Y, Zhao X, Wei W. Visible-light-mediated multi-component carbene transfer reactions of α-diazoesters to construct multisubstituted pyrazoles and 1,3-dicarbonyl derivatives. Org Chem Front . [DOI: 10.1039/d2qo01082h] [Reference Citation Analysis]
33 Zhao Y, Li L, Xu G, Xuan J. All‐Carbon Tetrasubstituted Olefins Synthesis from Diazo Compounds and Iodonium Ylides under Blue LED Irradiation. Adv Synth Catal 2022;364:506-11. [DOI: 10.1002/adsc.202101144] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
34 Zhang XJ, Zhang J, Xu YN, Li YM, Chi M, Yan Y, Wu RX, Zhang HR, Zhu YP. Cascade Wolff Rearrangement/Acylation: A Metal-Free and Eco-Friendly Approach for 4-Hydroxy-pyrazolo[3,4-b]pyridin-6-ones and N-Pyrazole Amides Synthesis from 5-Aminopyrazoles and α-Diazoketones. J Org Chem 2021;86:17471-81. [PMID: 34797656 DOI: 10.1021/acs.joc.1c02165] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
35 Stivanin ML, Duarte M, Leão LPMO, Saito FA, Jurberg ID. Visible-Light-Mediated Strategies for the Preparation of Oxime Ethers Derived from O-H Insertions of Oximes into Aryldiazoacetates. J Org Chem 2021;86:17528-32. [PMID: 34793163 DOI: 10.1021/acs.joc.1c02411] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
36 Munaretto LS, Dos Santos CY, Gallo RDC, Okada CY Jr, Deflon VM, Jurberg ID. Visible-Light-Mediated Strategies to Assemble Alkyl 2-Carboxylate-2,3,3-Trisubstituted β-Lactams and 5-Alkoxy-2,2,4-Trisubstituted Furan-3(2H)-ones Using Aryldiazoacetates and Aryldiazoketones. Org Lett 2021;23:9292-6. [PMID: 34797682 DOI: 10.1021/acs.orglett.1c03662] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
37 Cai BG, Li Q, Li L, Xuan J. Carbon-oxygen bond formation via visible-light-induced O–H insertion between acylsilanes and oximes. Green Synthesis and Catalysis 2021. [DOI: 10.1016/j.gresc.2021.12.004] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
38 Devi L, Pokhriyal A, Shekhar S, Kant R, Mukherjee S, Rastogi N. Organo‐photocatalytic Synthesis of 6‐ β ‐Disubstituted Phenanthridines from α ‐Diazo‐ β‐ Keto Compounds and Vinyl Azides. Asian J Org Chem 2021;10:3328-3333. [DOI: 10.1002/ajoc.202100518] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
39 Li F, Pei C, Koenigs RM. Photocatalytic gem-Difluoroolefination Reactions by a Formal C-C Coupling/Defluorination Reaction with Diazoacetates. Angew Chem Int Ed Engl 2021. [PMID: 34716734 DOI: 10.1002/anie.202111892] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 6.0] [Reference Citation Analysis]
40 Photons at Play: Photocatalysis in Sustainable Chemistry. A Joint Virtual Special Issue by ACS Catalysis and ACS Sustainable Chemistry & Engineering. ACS Sustainable Chem Eng 2021;9:13125-13127. [DOI: 10.1021/acssuschemeng.1c05667] [Reference Citation Analysis]
41 Tantillo DJ, Laconsay CJ. Melding of Experiment and Theory Illuminates Mechanisms of Metal-Catalyzed Rearrangements: Computational Approaches and Caveats. Synthesis 2021;53:3639-3652. [DOI: 10.1055/s-0040-1720451] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
42 Roy S, Kumar G, Chatterjee I. Photoinduced Diverse Reactivity of Diazo Compounds with Nitrosoarenes. Org Lett 2021;23:6709-13. [PMID: 34474577 DOI: 10.1021/acs.orglett.1c02279] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
43 Cai B, Li Q, Zhang Q, Li L, Xuan J. Synthesis of trisubstituted hydroxylamines by a visible light-promoted multicomponent reaction. Org Chem Front 2021;8:5982-7. [DOI: 10.1039/d1qo01102b] [Cited by in Crossref: 19] [Cited by in F6Publishing: 19] [Article Influence: 19.0] [Reference Citation Analysis]