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For: Chen L, Liu X, Zou Y. Recent Advances in the Construction of Phosphorus‐Substituted Heterocycles, 2009–2019. Adv Synth Catal 2020;362:1724-818. [DOI: 10.1002/adsc.201901540] [Cited by in Crossref: 39] [Cited by in F6Publishing: 49] [Article Influence: 19.5] [Reference Citation Analysis]
Number Citing Articles
1 Gryaznova TV, Nikanshina EO, Fayzullin RR, Islamov DR, Tarasov MV, Kholin KV, Budnikova YH. EPR-electrochemical monitoring of P–C coupling: Towards one-step electrochemical phosphorylation of acridine. Electrochimica Acta 2022. [DOI: 10.1016/j.electacta.2022.140946] [Reference Citation Analysis]
2 Li W, Shi R, Zhang X, Chen S, Wang Y, Wang M, Yang B, Li J, Xu XM. Different Lewis Acid Promotor-Steered Highly Regioselective Phosphorylation of Tertiary Enamides. J Org Chem 2022. [PMID: 35866754 DOI: 10.1021/acs.joc.2c00829] [Reference Citation Analysis]
3 Xu XM, Li W, Li Q, Chen S, Zhang X, Yang B, Wang WL. Manganese(III)-promoted highly stereoselective phosphorylation of acyclic tertiary enamides to synthesize E-selective β-phosphoryl enamides. Org Biomol Chem 2022;20:5566-74. [PMID: 35792054 DOI: 10.1039/d2ob00980c] [Reference Citation Analysis]
4 Wu W, Yan X, Li X, Ning Y, Hu L, Zhu L, Ouyang Q, Peng Y. Highly Enantioselective Synthesis of [1,2,4]Triazino[5,4-a]isoquinoline Derivatives via (3 + 3) Cycloaddition Reactions of Diazo Compounds and Isoquinolinium Methylides. Org Lett 2022. [PMID: 35604766 DOI: 10.1021/acs.orglett.2c01122] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Zheng SL, Wen Z, Yang KC, Zeng Y, Chen L, Deng JF. Copper(II)-catalyzed direct dehydrative alkynylation of 2H-chromene hemiketals with terminal alkynes to 2,2-disubstituted 2-alkynylated 2H-chromenes. Org Biomol Chem 2022;20:3785-9. [PMID: 35438703 DOI: 10.1039/d2ob00481j] [Reference Citation Analysis]
6 Guo S, Yan W, Zhang Z, Huang Z, Guo Y, Liang Z, Li S, Fu Z, Cai H. Nickel-Catalyzed 1,1-Dihydrophosphinylation of Nitriles with Phosphine Oxides. J Org Chem 2022. [PMID: 35468296 DOI: 10.1021/acs.joc.1c02815] [Reference Citation Analysis]
7 Zheng L, Cai L, Mei W, Liu G, Deng L, Zou X, Zhuo X, Zhong Y, Guo W. Copper-Catalyzed Phosphorylation of N,N-Disubstituted Hydrazines: Synthesis of Multisubstituted Phosphorylhydrazides as Potential Anticancer Agents. J Org Chem 2022. [PMID: 35442041 DOI: 10.1021/acs.joc.2c00452] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
8 Saha S, Bagdi AK. Visible light-promoted photocatalyst-free activation of persulfates: a promising strategy for C-H functionalization reactions. Org Biomol Chem 2022;20:3249-62. [PMID: 35363233 DOI: 10.1039/d2ob00109h] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
9 Yu Y, Wang Y, Li B, Tan Y, Zhao H, Li Z, Zhang C, Ma W. Ruthenium‐Catalyzed Vinylene Carbonate Annulation by C−H/N−H Functionalizations: Step‐Economical Access to Indoles. Adv Synth Catal. [DOI: 10.1002/adsc.202101466] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
10 Sarva S, Dunnutala R, Tellamekala S, Gundluru M, Cirandur SR. Green synthesis and antimicrobial activity of substituted diethyl (((5-(ethylthio)-1,3,4-thiadiazol-2-yl)amino)(phenyl)methyl)phosphonates. Synthetic Communications. [DOI: 10.1080/00397911.2021.2020844] [Reference Citation Analysis]
11 Yu B, Huang H. Recent Advances in C—X Bond Metathesis Reactions. Chinese Journal of Organic Chemistry 2022;42:2376. [DOI: 10.6023/cjoc202202003] [Reference Citation Analysis]
12 Li Q, Zhao C, Chen T, Han L. Direct phosphorylation of benzylic C–H bonds under transition metal-free conditions forming sp 3 C–P bonds. RSC Adv 2022;12:18441-4. [DOI: 10.1039/d2ra02812c] [Reference Citation Analysis]
13 Zhu P, Yang Y, Li Y, Zhu J, Wu L. Electrochemical Oxidative C H Phosphonylation of thiazole derivatives in ambient conditions. Molecular Catalysis 2022;517:112022. [DOI: 10.1016/j.mcat.2021.112022] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
14 Mondal A, Thiel NO, Dorel R, Feringa BL. P-chirogenic phosphorus compounds by stereoselective Pd-catalysed arylation of phosphoramidites. Nat Catal 2022;5:10-9. [DOI: 10.1038/s41929-021-00697-9] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
15 Fuertes M, Selas A, Trejo A, Knudsen BR, Palacios F, Alonso C. Synthesis of hybrid phosphorated indenoquinolines and biological evaluation as topoisomerase I inhibitors and antiproliferative agents. Bioorg Med Chem Lett 2021;57:128517. [PMID: 34952177 DOI: 10.1016/j.bmcl.2021.128517] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
16 Mo K, Zhou X, Wu J, Zhao Y. Radical-induced denitration of N-(p-nitrophenyl)propiolamides coupled with dearomatization: access to phosphonylated/trifluoromethylated azaspiro[4.5]-trienones. Chem Commun (Camb) 2021. [PMID: 34913445 DOI: 10.1039/d1cc05724c] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
17 Zheng SL, Chen L. Synthesis of 2H-chromenes: recent advances and perspectives. Org Biomol Chem 2021;19:10530-48. [PMID: 34842267 DOI: 10.1039/d1ob01906f] [Cited by in F6Publishing: 3] [Reference Citation Analysis]
18 Hore S, Singh RP. Phosphorylation of arenes, heteroarenes, alkenes, carbonyls and imines by dehydrogenative cross-coupling of P(O)-H and P(R)-H. Org Biomol Chem 2021. [PMID: 34904988 DOI: 10.1039/d1ob02003j] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
19 Tay NES, Lehnherr D, Rovis T. Photons or Electrons? A Critical Comparison of Electrochemistry and Photoredox Catalysis for Organic Synthesis. Chem Rev 2021. [PMID: 34751568 DOI: 10.1021/acs.chemrev.1c00384] [Cited by in F6Publishing: 24] [Reference Citation Analysis]
20 Yang F, Zhou Q, Wang H, Tang L. Copper‐Catalyzed Cross‐Dehydrogenative Phosphorylation of 2‐Amino‐1,4‐naphthoquinones with H ‐Phosphonates. Eur J Org Chem 2021;2021:5618-22. [DOI: 10.1002/ejoc.202100870] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
21 Chen Y, Zhang S, Xue Y, Mo L, Zhang Z. Palladium anchored on a covalent organic framework as a heterogeneous catalyst for phosphorylation of aryl bromides. Applied Organom Chemis 2022;36. [DOI: 10.1002/aoc.6480] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
22 Zhang X, Qi X, Wu Y, Liu P, He Y. P-stereogenic N-vinylphosphonamides enabled by asymmetric allylic substitution-isomerization. Cell Reports Physical Science 2021;2:100594. [DOI: 10.1016/j.xcrp.2021.100594] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
23 Zhao L, Sun M, Yang F, Wu Y. Silver(I) Promoted the C4-H Bond Phosphonation of 1-Naphthylamine Derivatives with H-Phosphonates. J Org Chem 2021;86:11519-30. [PMID: 34383506 DOI: 10.1021/acs.joc.1c00971] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
24 Ghosh A, Dey R, Banerjee P. Relieving the stress together: annulation of two different strained rings towards the formation of biologically significant heterocyclic scaffolds. Chem Commun (Camb) 2021;57:5359-73. [PMID: 33969833 DOI: 10.1039/d1cc00998b] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
25 Fan T, Liu Y, Jiang C, Xu Y, Chen Y. A metal-free radical cascade reaction of phosphine oxides with 2-aryloxy phenylacetylenes to synthesize diphosphonyl xanthene derivatives. Org Biomol Chem 2021;19:6609-12. [PMID: 34263284 DOI: 10.1039/d1ob01045j] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
26 Tajti Á, Szabó KE, Popovics-Tóth N, Iskanderov J, Perdih F, Hackler L, Kari B, Puskás LG, Bálint E. PMDTA-catalyzed multicomponent synthesis and biological activity of 2-amino-4H-chromenes containing a phosphonate or phosphine oxide moiety. Org Biomol Chem 2021;19:6883-91. [PMID: 34324620 DOI: 10.1039/d1ob01204e] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
27 Zheng SL, Zou YX, Wen Z, Lin JF, Gu LH, Chen L. Y(OTf)3-catalyzed phosphorylation of 2H-chromene hemiacetals with P(O)-H compounds to 2-phosphorylated 2H-chromenes. Org Biomol Chem 2021;19:6812-6. [PMID: 34297020 DOI: 10.1039/d1ob01221e] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
28 Chen L, Zou Y. Recent Advances in the Direct Functionalization of Isoindolinones for the Synthesis of 3,3‐Disubstituted Isoindolinones. Adv Synth Catal 2021;363:4159-76. [DOI: 10.1002/adsc.202100522] [Cited by in Crossref: 2] [Cited by in F6Publishing: 9] [Article Influence: 2.0] [Reference Citation Analysis]
29 Li J, Zhang S, Lao J, Zou H. Direct Transition-Metal Free Benzene C-H Functionalization by Intramolecular Non-Nitroarene Nucleophilic Aromatic Substitution of Hydrogen to Diverse AIEgens. ChemSusChem 2021;14:3208-18. [PMID: 34132487 DOI: 10.1002/cssc.202101109] [Reference Citation Analysis]
30 Chen X, Wu H, Yu R, Zhu H, Wang Z. Palladium-Catalyzed C-P(III) Bond Formation by Coupling ArBr/ArOTf with Acylphosphines. J Org Chem 2021;86:8987-96. [PMID: 34115513 DOI: 10.1021/acs.joc.1c00937] [Cited by in F6Publishing: 5] [Reference Citation Analysis]
31 Guo L, Su M, Zhan H, Liu W, Wang S. Silver‐Catalyzed Direct Regioselective C3 Phosphonation of 4 H ‐pyrido[1,2‐ a ]pyrimidin‐4‐ones With H ‐phosphites. Asian J of Organic Chemis 2021;10:1660-4. [DOI: 10.1002/ajoc.202100235] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
32 An D, Sang J, Hu R, Chen J, Feng L, Rao W. Synthesis of 2‐Phosphoryl‐3‐Monofluorovinylindoles under Catalyst‐ and Additive‐Free Conditions. Adv Synth Catal 2021;363:3496-501. [DOI: 10.1002/adsc.202100331] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
33 Shi X, Wang Z, Li Y, Li X, Li X, Shi D. Palladium-Catalyzed Remote C-H Phosphonylation of Indoles at the C4 and C6 Positions by a Radical Approach. Angew Chem Int Ed Engl 2021;60:13871-6. [PMID: 33851763 DOI: 10.1002/anie.202103395] [Cited by in Crossref: 1] [Cited by in F6Publishing: 6] [Article Influence: 1.0] [Reference Citation Analysis]
34 Kittikool T, Phakdeeyothin K, Chantarojsiri T, Yotphan S. Manganese‐Promoted Regioselective Direct C3 ‐Phosphinoylation of 2‐Pyridones. Eur J Org Chem 2021;2021:3071-8. [DOI: 10.1002/ejoc.202100336] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
35 Tao ZK, Li CK, Li JA, Shoberu A, Zhang W, Zou JP. Copper-Catalyzed Vicinal Cyano-, Thiocyano-, and Chlorophosphorylation of Alkynes: A Phosphinoyl Radical-Initiated Approach for Difunctionalized Alkenes. Org Lett 2021;23:4342-7. [PMID: 34029107 DOI: 10.1021/acs.orglett.1c01286] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
36 Zhang S, Del Vecchio A, Kuniyil R, Messinis AM, Lin Z, Ackermann L. Electrocatalytic C–H phosphorylation through nickel(III/IV/II) catalysis. Chem 2021;7:1379-92. [DOI: 10.1016/j.chempr.2021.04.009] [Cited by in Crossref: 4] [Cited by in F6Publishing: 6] [Article Influence: 4.0] [Reference Citation Analysis]
37 Chen L, Liu X, Zhang J, Duan L, Wen Z, Ni H. Relay Cu(I)/Brønsted Base Catalysis for Phospha ‐Michael Addition/5‐ exodig Cyclization/Isomerization of in situ Formed aza ‐Alkynyl o‐ quinone methides with P(O)−H compounds to C3‐Phosphorylated Indoles. Adv Synth Catal 2021;363:3006-12. [DOI: 10.1002/adsc.202100275] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
38 Gbubele JD, Olszewski TK. Asymmetric synthesis of organophosphorus compounds using H-P reagents derived from chiral alcohols. Org Biomol Chem 2021;19:2823-46. [PMID: 33710223 DOI: 10.1039/d1ob00124h] [Cited by in Crossref: 1] [Cited by in F6Publishing: 8] [Article Influence: 1.0] [Reference Citation Analysis]
39 Modranka J, Drogosz-Stachowicz J, Pietrzak A, Janecka A, Janecki T. Synthesis and structure-activity relationship study of novel 3-diethoxyphosphorylfuroquinoline-4,9-diones with potent antitumor efficacy. Eur J Med Chem 2021;219:113429. [PMID: 33852973 DOI: 10.1016/j.ejmech.2021.113429] [Cited by in F6Publishing: 4] [Reference Citation Analysis]
40 Wang S, Xue Q, Guan Z, Ye Y, Lei A. Mn-Catalyzed Electrooxidative Undirected C–H/P–H Cross-Coupling between Aromatics and Diphenyl Phosphine Oxides. ACS Catal 2021;11:4295-300. [DOI: 10.1021/acscatal.1c00549] [Cited by in Crossref: 18] [Cited by in F6Publishing: 17] [Article Influence: 18.0] [Reference Citation Analysis]
41 Teixeira FC, Lucas C, Curto MJM, André V, Duarte MT, Teixeira APS. Synthesis of novel pyrazolo[3,4-b]quinolinebisphosphonic acids and an unexpected intramolecular cyclization and phosphonylation reaction. Org Biomol Chem 2021;19:2533-45. [PMID: 33666215 DOI: 10.1039/d1ob00025j] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
42 Chen L, Zou Y, Zheng S, Liu X, Yang H, Zhang J, Zeng Y, Duan L, Wen Z, Ni H. Dearomative 1,6-addition of P(O)–H to in situ formed p -QM-like ion pairs from 2-benzofuryl-ols to C3-phosphinoyl hydrobenzofurans. Org Chem Front 2021;8:1756-63. [DOI: 10.1039/d1qo00076d] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
43 Shen J, Zhang Y, Yu Y, Wang M. Metal-free visible-light-induced photoredox-catalyzed intermolecular pyridylation/phosphinoylation of alkenes. Org Chem Front 2021;8:901-7. [DOI: 10.1039/d0qo01218a] [Cited by in Crossref: 6] [Cited by in F6Publishing: 10] [Article Influence: 6.0] [Reference Citation Analysis]
44 Kong Y, Kim JK, Li Y, Zhang J, Huang M, Wu Y. An oxidant- and catalyst-free electrooxidative cross-coupling approach to 3-tetrahydroisoquinoline substituted coumarins. Green Chem 2021;23:1274-9. [DOI: 10.1039/d0gc03930f] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 7.0] [Reference Citation Analysis]
45 Ivanov SM, Mironovich LM, Kolotyrkina NG, Minyaev ME. Synthesis of (3-tert-Butylpyrazolo[5,1-c][1,2,4]triazin-4-yl)phosphine Oxides. Russ J Org Chem 2021;57:47-57. [DOI: 10.1134/s1070428021010073] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 5.0] [Reference Citation Analysis]
46 Ung SP, Mechrouk VA, Li C. Shining Light on the Light-Bearing Element: A Brief Review of Photomediated C–H Phosphorylation Reactions. Synthesis 2021;53:1003-22. [DOI: 10.1055/s-0040-1705978] [Cited by in Crossref: 5] [Cited by in F6Publishing: 8] [Article Influence: 2.5] [Reference Citation Analysis]
47 Sharma UK, Ranjan P, Van der Eycken EV, You SL. Sequential and direct multicomponent reaction (MCR)-based dearomatization strategies. Chem Soc Rev 2020;49:8721-48. [PMID: 33079105 DOI: 10.1039/d0cs00128g] [Cited by in Crossref: 12] [Cited by in F6Publishing: 35] [Article Influence: 6.0] [Reference Citation Analysis]
48 Zou Y, Ni H, Dong H, Yang X, Chen L. A HClO 4 ‐Catalyzed Substitutive Phosphorylation of Anthracene‐9‐ols with P(O)−H Compounds to Phosphorylated 9,10‐Dihydroanthracenes. Asian J Org Chem 2020;9:2196-200. [DOI: 10.1002/ajoc.202000385] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
49 Sbei N, Martins GM, Shirinfar B, Ahmed N. Electrochemical Phosphorylation of Organic Molecules. Chem Rec 2020;20:1530-52. [DOI: 10.1002/tcr.202000096] [Cited by in Crossref: 6] [Cited by in F6Publishing: 12] [Article Influence: 3.0] [Reference Citation Analysis]
50 Brahmachari G. Catalyst‐ and Additive‐Free Decarboxylative C‐4 Phosphorylation of Coumarin‐3‐Carboxylic Acids at Ambient Conditions. Adv Synth Catal 2020;362:5411-21. [DOI: 10.1002/adsc.202001054] [Cited by in Crossref: 3] [Cited by in F6Publishing: 9] [Article Influence: 1.5] [Reference Citation Analysis]
51 Lei T, Liang G, Cheng YY, Chen B, Tung CH, Wu LZ. Cobaloxime Catalysis for Enamine Phosphorylation with Hydrogen Evolution. Org Lett 2020;22:5385-9. [PMID: 32585106 DOI: 10.1021/acs.orglett.0c01709] [Cited by in Crossref: 5] [Cited by in F6Publishing: 16] [Article Influence: 2.5] [Reference Citation Analysis]