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For: Tian L, Wan J, Sheng S. Transition Metal‐free C−H Sulfonylation and Pyrazole Annulation Cascade for the Synthesis of 4‐Sulfonyl Pyrazoles. ChemCatChem 2020;12:2533-7. [DOI: 10.1002/cctc.202000244] [Cited by in Crossref: 24] [Cited by in F6Publishing: 25] [Article Influence: 12.0] [Reference Citation Analysis]
Number Citing Articles
1 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]
2 Hu SJ, Jiang LL, Qiu H, Luo CM, Guan YT, Li L, Dong Y, Lei KW, Wei WT. Cyclization/hydrolysis of 1,5-enenitriles initiated by sulfonyl radicals in the aqueous phase in the presence of the I2/TBHP system. Org Biomol Chem 2022. [PMID: 35876742 DOI: 10.1039/d2ob01124g] [Reference Citation Analysis]
3 Yang X, Sun J, Huang X, Jin Z. Asymmetric Synthesis of Structurally Sophisticated Spirocyclic Pyrano[2,3-c]pyrazole Derivatives Bearing a Chiral Quaternary Carbon Center. Org Lett 2022. [PMID: 35857420 DOI: 10.1021/acs.orglett.2c02211] [Reference Citation Analysis]
4 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]
5 Fu L, Wan JP, Zhou L, Liu Y. Copper-catalyzed C-H/N-H annulation of enaminones and alkynyl esters for densely substituted pyrrole synthesis. Chem Commun (Camb) 2022;58:1808-11. [PMID: 35040446 DOI: 10.1039/d1cc06768k] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 11.0] [Reference Citation Analysis]
6 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]
7 Elgemeie GH, Azzam RA, Zaghary WA, Aly AA, Metwally NH, Sarhan MO, Abdelhafez EM, Elsayed RE. Synthesis of N-sulfonated N-diazoles, their chemistry and biological assessments. N-Sulfonated-N-Heterocycles 2022. [DOI: 10.1016/b978-0-12-822179-2.00014-8] [Reference Citation Analysis]
8 Geng M, Kuang J, Fang W, Miao M, Ma Y. Facile construction of C,N-disulfonated 5-amino pyrazoles through an iodine-catalyzed cascade reaction. Org Biomol Chem 2022;20:8187-8191. [DOI: 10.1039/d2ob01647h] [Reference Citation Analysis]
9 Guo H, Tian L, Liu Y, Wan JP. DMSO as a C1 Source for [2 + 2 + 1] Pyrazole Ring Construction via Metal-Free Annulation with Enaminones and Hydrazines. Org Lett 2021. [PMID: 34908420 DOI: 10.1021/acs.orglett.1c03879] [Cited by in Crossref: 15] [Cited by in F6Publishing: 20] [Article Influence: 15.0] [Reference Citation Analysis]
10 Tsogoeva SB, Dong G, Ackermann L. Editorial: The Catalysis of Ring Synthesis. ChemCatChem 2021;13:2962-2964. [DOI: 10.1002/cctc.202100449] [Reference Citation Analysis]
11 Duan X, Li H, Li W, Wang J, Liu N. NBS‐Promoted C−H Amination of Enaminones for the Synthesis of N‐Heterocycle Substituted Enaminones**. ChemistrySelect 2021;6:6478-82. [DOI: 10.1002/slct.202101726] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Chen J, Chen D, Kuang J, Ma Y. Transition Metal-Free De Novo Synthesis of Sulfonated Pyrazoles from Sulfonyl Hydrazides, 1,3-Diketones, and Sodium Sulfinates at Room Temperature. J Org Chem 2021;86:9289-98. [PMID: 34185538 DOI: 10.1021/acs.joc.1c00171] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 6.0] [Reference Citation Analysis]
13 Devi J, Saikia N, Choudhury G, Deka DC. Iodine catalyzed regioselective sulfenylation of aminouracils with sulfonyl hydrazides. Tetrahedron Letters 2021;65:152753. [DOI: 10.1016/j.tetlet.2020.152753] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
14 Tian S, Luo T, Zhu Y, Wan J. Recent advances in the diversification of chromones and flavones by direct C H bond activation or functionalization. Chinese Chemical Letters 2020;31:3073-82. [DOI: 10.1016/j.cclet.2020.07.042] [Cited by in Crossref: 32] [Cited by in F6Publishing: 18] [Article Influence: 16.0] [Reference Citation Analysis]
15 Dong D, Han Q, Yang S, Song J, Li N, Wang Z, Xu X. Recent Progress in Sulfonylation via Radical Reaction with Sodium Sulfinates, Sulfinic Acids, Sulfonyl Chlorides or Sulfonyl Hydrazides. ChemistrySelect 2020;5:13103-34. [DOI: 10.1002/slct.202003650] [Cited by in Crossref: 27] [Cited by in F6Publishing: 28] [Article Influence: 13.5] [Reference Citation Analysis]
16 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: 16.0] [Reference Citation Analysis]
17 Li Y, Wan J, Liu Y. Annulation of Ketene Dithioacetals and Sulfonyl Hydrazines for the Synthesis of N ‐Sulfonyl 5‐Alkylthiopyrazoles. ChemistrySelect 2020;5:9431-4. [DOI: 10.1002/slct.202002480] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
18 Deng L, Liu Y, Zhu Y, Wan J. Transition‐Metal‐Free Annulation of Enamines and Tosyl Azide toward N‐Heterocycle Fused and 5‐Amino‐1,2,3‐Triazoles. Eur J Org Chem 2020;2020:5606-9. [DOI: 10.1002/ejoc.202000938] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 4.5] [Reference Citation Analysis]
19 Gan L, Wei L, Wan J. Catalyst‐Free Synthesis of α‐Diazoketones in Water by Microwave Promoted Enaminone C=C Double Bond Cleavage. ChemistrySelect 2020;5:7822-5. [DOI: 10.1002/slct.202002247] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 5.0] [Reference Citation Analysis]
20 Feng Z, Li J, Jiang Y, Tian Y, Xu G, Shi X, Ding Q, Li W, Ma C, Yu B. Transition-metal-free sulfonylations of methylthiolated alkynones to synthesize 3-sulfonylated thioflavones. New J Chem 2020;44:14786-90. [DOI: 10.1039/d0nj03386c] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 5.0] [Reference Citation Analysis]