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For: Huang J, Yu F. Recent Advances in Organic Synthesis Based on N,N-Dimethyl Enaminones. Synthesis 2021;53:587-610. [DOI: 10.1055/s-0040-1707328] [Cited by in Crossref: 32] [Cited by in F6Publishing: 24] [Article Influence: 10.7] [Reference Citation Analysis]
Number Citing Articles
1 Li X, Chen Z, Chen W, Xie X, Zhou H, Liao Y, Yu F, Huang J. B2pin2-Mediated Cascade Cyclization/Aromatization Reaction: Facial Access to Functionalized Indolizines. Org Lett 2022. [PMID: 36173232 DOI: 10.1021/acs.orglett.2c02905] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
2 Feng J, Wang Y, Gao L, Yu Y, Baell JB, Huang F. Electrochemical Synthesis of Polysubstituted Sulfonated Pyrazoles via Cascade Intermolecular Condensation, Radical-Radical Cross Coupling Sulfonylation, and Pyrazole Annulation. J Org Chem 2022. [PMID: 36166815 DOI: 10.1021/acs.joc.2c01609] [Reference Citation Analysis]
3 Rao K, Chai Z, Zhou P, Liu D, Sun Y, Yu F. Transition-metal-free approach to quinolines via direct oxidative cyclocondensation reaction of N,N-dimethyl enaminones with o-aminobenzyl alcohols. Front Chem 2022;10:1008568. [DOI: 10.3389/fchem.2022.1008568] [Reference Citation Analysis]
4 Li X, Chen Z, Liu Y, Luo N, Chen W, Liu C, Yu F, Huang J. Nickel-Catalyzed Reductive Borylation of Enaminones via C(sp2)-N Bond Cleavage. J Org Chem 2022. [PMID: 35895906 DOI: 10.1021/acs.joc.2c00096] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
5 Yuan L, Liu J, Huang K, Wang S, Jin Y, Lin J. Cascade Reaction of Tertiary Enaminones, KSCN, and Anilines: Temperature-Controlled Synthesis of 2-Aminothiazoles and 2-Iminothiazoline. J Org Chem 2022. [PMID: 35786913 DOI: 10.1021/acs.joc.2c00918] [Reference Citation Analysis]
6 Poletto J, da Silva MJV, Pianoski KE, Willig JCM, Rosa FA. Regiodivergent Synthesis of 3,4- and 4,5-Disubstituted N-Methylpyrazoles from 4-Acyl-1H-pyrrole-2,3-dione and Methylhydrazine. J Org Chem 2022. [PMID: 35687873 DOI: 10.1021/acs.joc.2c00657] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Mokkarat A, Kruanetr S, Sakee U. Facial preparation of trifluoroacetic acid-immobilized amino-functionalized silica magnetite nano-catalysts as a highly efficient and reusable for synthesis of β-enaminones. Journal of Molecular Structure 2022;1259:132745. [DOI: 10.1016/j.molstruc.2022.132745] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
8 Liu Y, Zhang T, Wan JP. Ultrasound-Promoted Synthesis of α-Thiocyanoketones via Enaminone C═C Bond Cleavage and Tunable One-Pot Access to 4-Aryl-2-aminothiazoles. J Org Chem 2022. [PMID: 35616657 DOI: 10.1021/acs.joc.2c00708] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
9 Wang Z, Zhao B, Liu Y, Wan J. Recent Advances in Reactions Using Enaminone in Water or Aqueous Medium. Adv Synth Catal 2022;364:1508-21. [DOI: 10.1002/adsc.202200144] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 7.0] [Reference Citation Analysis]
10 Wang Y, Zhang C, Li S, Liu L, Feng X. Recent Advances in Transition Metal Catalyzed Synthesis of β ‐Enaminones and β ‐Enaminoesters. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202103345] [Reference Citation Analysis]
11 Ying J, Liu T, Liu Y, Wan JP. Base-Promoted Annulative Difluoromethylenation of Enaminones with BrCF2CO2Et toward 2,2-Difluorinated 2,3-Dihydrofurans. Org Lett 2022. [PMID: 35302379 DOI: 10.1021/acs.orglett.2c00671] [Cited by in Crossref: 5] [Cited by in F6Publishing: 10] [Article Influence: 5.0] [Reference Citation Analysis]
12 Zhang C, Luo J, Zhang J, Chen L, Zhu X, Guo M, Shen C, Li Z, Wang W. Tf 2 O‐mediated Regioselective C(sp 2 )−H Sulfenylation of Enaminones Using Methyl Sulfoxides as Sulfur Sources. Asian J of Organic Chemis. [DOI: 10.1002/ajoc.202200014] [Reference Citation Analysis]
13 Liu Z, Sun S, Lou J. PhIO-Mediated Oxidative C═C Bond Cleavage and Reassembly toward Highly Functionalized Oxazolones. Org Lett 2022. [PMID: 35129353 DOI: 10.1021/acs.orglett.1c04326] [Reference Citation Analysis]
14 Cheng D, Yu C, Pu Y, Xu X. DDQ-mediated oxidative coupling reaction of N,N-dimethyl enaminones with cycloheptatriene. Tetrahedron Letters 2022;90:153609. [DOI: 10.1016/j.tetlet.2021.153609] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
15 Wang ZW, Zheng Y, Qian YE, Guan JP, Lu WD, Yuan CP, Xiao JA, Chen K, Xiang HY, Yang H. Photoredox-Catalyzed Cascade of o-Hydroxyarylenaminones to Access 3-Aminated Chromones. J Org Chem 2022. [PMID: 35014269 DOI: 10.1021/acs.joc.1c02796] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
16 Santos CM, Silva AM. Recent advances in the synthesis of 4H-chromen-4-ones (2012 − 2021). Advances in Heterocyclic Chemistry 2022. [DOI: 10.1016/bs.aihch.2022.02.001] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
17 Suresh S, Bhimrao Patil P, Yu P, Fang C, Weng Y, Kavala V, Yao C. A Study of the Reactions of 3‐Bromopropenals with Anilines for the Synthesis of α‐Bromo Enaminones. Adv Synth Catal 2021;363:4915-4925. [DOI: 10.1002/adsc.202100779] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
18 Zhang C, Guo H, Chen L, Zhang J, Guo M, Zhu X, Shen C, Li Z. One-Pot Synthesis of Symmetrical and Asymmetrical 3-Amino Diynes via Cu(I)-Catalyzed Reaction of Enaminones with Terminal Alkynes. Org Lett 2021;23:8169-73. [PMID: 34636564 DOI: 10.1021/acs.orglett.1c02848] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
19 Mittersteiner M, Farias FFS, Bonacorso HG, Martins MAP, Zanatta N. Ultrasound-assisted synthesis of pyrimidines and their fused derivatives: A review. Ultrason Sonochem 2021;79:105683. [PMID: 34562732 DOI: 10.1016/j.ultsonch.2021.105683] [Cited by in Crossref: 11] [Cited by in F6Publishing: 8] [Article Influence: 5.5] [Reference Citation Analysis]
20 Osyanin VA, Korzhenko KS, Rashchepkina DA, Osipov DV, Klimochkin YN. Nucleophilic Vinylic Substitution in Perfluoroacylchromenes. Diastereoselective Synthesis of Push–Pull Enamino Ketones. Russ J Org Chem 2021;57:1053-62. [DOI: 10.1134/s1070428021070046] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
21 Liu T, Wei L, Zhao B, Liu Y, Wan JP. Copper-Catalyzed Enaminone C(sp2)-N Bond Phosphonation for Stereoselective Synthesis of Alkenylphosphonates. J Org Chem 2021;86:9861-8. [PMID: 34189914 DOI: 10.1021/acs.joc.1c00862] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 5.0] [Reference Citation Analysis]
22 Xu Z, Fu L, Fang X, Huang B, Zhou L, Wan JP. Tunable Trifunctionalization of Tertiary Enaminones for the Regioselective and Metal-Free Synthesis of Discrete and Proximal Phosphoryl Nitriles. Org Lett 2021;23:5049-53. [PMID: 34137270 DOI: 10.1021/acs.orglett.1c01581] [Cited by in Crossref: 8] [Cited by in F6Publishing: 11] [Article Influence: 4.0] [Reference Citation Analysis]
23 Jiang Z, Zhou J, Zhu H, Liu H, Zhou Y. Rh(III)-Catalyzed [5 + 1] Annulation of Indole-enaminones with Diazo Compounds To Form Highly Functionalized Carbazoles. Org Lett 2021;23:4406-10. [PMID: 34018745 DOI: 10.1021/acs.orglett.1c01341] [Cited by in Crossref: 12] [Cited by in F6Publishing: 14] [Article Influence: 6.0] [Reference Citation Analysis]
24 Dalinger IL, Shkineva TK, Vatsadze IA, Kormanov AV, Kozeev AM, Suponitsky KY, Pivkina AN, Sheremetev AB. Novel energetic CNO oxidizer: Pernitro-substituted pyrazolyl-furazan framework. FirePhysChem 2021;1:83-9. [DOI: 10.1016/j.fpc.2021.04.005] [Cited by in Crossref: 13] [Cited by in F6Publishing: 15] [Article Influence: 6.5] [Reference Citation Analysis]
25 Korkmaz A, Duran S. High yielding electrophilic amination with lower order and higher order organocuprates: Application of acetone O-(4-Chlorophenylsulfonyl)oxime in the construction of the C−N bond at room temperature. Synthetic Communications 2021;51:2077-87. [DOI: 10.1080/00397911.2021.1924787] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
26 Chen XB, Huang ST, Li J, Yang Q, Yang L, Yu F. Highly Regioselective and Chemoselective [3 + 3] Annulation of Enaminones with ortho-Fluoronitrobenzenenes: Divergent Synthesis of Aposafranones and Their N-Oxides. Org Lett 2021;23:3032-7. [PMID: 33792341 DOI: 10.1021/acs.orglett.1c00710] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]
27 Mkrtchyan S, Iaroshenko VO. Arylation of ortho-Hydroxyarylenaminones by Sulfonium Salts and Arenesulfonyl Chlorides: An Access to Isoflavones. J Org Chem 2021;86:4896-916. [PMID: 33721488 DOI: 10.1021/acs.joc.0c02294] [Cited by in Crossref: 9] [Cited by in F6Publishing: 10] [Article Influence: 4.5] [Reference Citation Analysis]
28 Zhang B, Liu D, Sun Y, Zhang Y, Feng J, Yu F. Preparation of Thiazole-2-thiones through TBPB-Promoted Oxidative Cascade Cyclization of Enaminones with Elemental Sulfur. Org Lett 2021;23:3076-82. [DOI: 10.1021/acs.orglett.1c00751] [Cited by in Crossref: 18] [Cited by in F6Publishing: 20] [Article Influence: 9.0] [Reference Citation Analysis]