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For: Yugandhar D, Nayak VL, Archana S, Shekar KC, Srivastava AK. Design, synthesis and anticancer properties of novel oxa/azaspiro[4,5]trienones as potent apoptosis inducers through mitochondrial disruption. European Journal of Medicinal Chemistry 2015;101:348-57. [DOI: 10.1016/j.ejmech.2015.06.050] [Cited by in Crossref: 35] [Cited by in F6Publishing: 31] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 Yuan J, Wei K, Zhang G, Chen N, Wei X, Pan C, Mo D, Su G. Cryptolepine and aromathecin based mimics as potent G-quadruplex-binding, DNA-cleavage and anticancer agents: Design, synthesis and DNA targeting-induced apoptosis. European Journal of Medicinal Chemistry 2019;169:144-58. [DOI: 10.1016/j.ejmech.2019.02.072] [Cited by in Crossref: 13] [Cited by in F6Publishing: 11] [Article Influence: 4.3] [Reference Citation Analysis]
2 Chen Y, Chen Y, Guan Z, He Y. Visible-light-mediated selective thiocyanation/ipso-cyclization/oxidation cascade for the synthesis of thiocyanato-containing azaspirotrienediones. Tetrahedron 2019;75:130763. [DOI: 10.1016/j.tet.2019.130763] [Cited by in Crossref: 7] [Article Influence: 2.3] [Reference Citation Analysis]
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4 Wu J, Ma D, Tang G, Zhao Y. Copper-Catalyzed Phosphonylation/Trifluoromethylation of N-p-NO2-Benzoylacrylamides Coupled with Dearomatization and Denitration. Org Lett 2019;21:7674-8. [PMID: 31496252 DOI: 10.1021/acs.orglett.9b03034] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 2.3] [Reference Citation Analysis]
5 Mantovani AC, Hernández JG, Bolm C. Synthesis of 3-Iodobenzofurans by Electrophilic Cyclization under Solventless Conditions in a Ball Mill: Synthesis of 3-Iodobenzofurans by Electrophilic Cyclization under Solventless Conditions in a Ball Mill. Eur J Org Chem 2018;2018:2458-61. [DOI: 10.1002/ejoc.201800027] [Cited by in Crossref: 7] [Cited by in F6Publishing: 3] [Article Influence: 1.8] [Reference Citation Analysis]
6 Zhang Y, Deng C, Zhou W, Zhou L, Cao Q, Shen W, Liang H, Chen Z. Synthesis and in vitro antitumor activity evaluation of copper(II) complexes with 5-pyridin-2-yl-[1,3]dioxolo[4,5-g]isoquinoline derivatives. Journal of Inorganic Biochemistry 2019;201:110820. [DOI: 10.1016/j.jinorgbio.2019.110820] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
7 Reddy CR, Yarlagadda S, Ramesh B, Reddy MR, Sridhar B, Reddy BVS. Na 2 S 2 O 8 ‐Promoted Radical Cyclization for the Synthesis of Azaspiro[4.5]deca‐3,6,9‐triene‐2,8‐dione and Pyrrolo[2,1‐ j ]quinolone Derivatives. Eur J Org Chem 2017;2017:2332-7. [DOI: 10.1002/ejoc.201700058] [Cited by in Crossref: 11] [Cited by in F6Publishing: 7] [Article Influence: 2.2] [Reference Citation Analysis]
8 Yi Q, Wang Y, He M, Zhang W, Du F, Gu Y, Bai L, Liu Y. Induction of apoptosis in SGC-7901 cells by ruthenium(II) complexes through ROS-mediated lysosome–mitochondria dysfunction and inhibition of PI3K/AKT/mTOR pathways. Transit Met Chem 2019;44:187-205. [DOI: 10.1007/s11243-018-0283-8] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
9 Hergert T, Varga B, Thurner A, Faigl F, Mátravölgyi B. Copper-facilitated Suzuki-Miyaura coupling for the preparation of 1,3-dioxolane-protected 5-arylthiophene-2-carboxaldehydes. Tetrahedron 2018;74:2002-8. [DOI: 10.1016/j.tet.2018.03.001] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
10 Liu T, Li Y, Jiang L, Wang J, Jin K, Zhang R, Duan C. Photo-mediated synthesis of halogenated spiro[4,5]trienones of N-aryl alkynamides with PhI(OCOCF3)2 and KBr/KCl. Org Biomol Chem 2020;18:1933-9. [PMID: 32101242 DOI: 10.1039/d0ob00057d] [Cited by in Crossref: 7] [Article Influence: 3.5] [Reference Citation Analysis]
11 Pluta K, Szmielew M, Suwińska K, Latocha M. Synthesis, spectroscopic structure identification, X-ray study and anticancer activities of new angularly fused quinobenzothiazines. Journal of Molecular Structure 2016;1122:62-71. [DOI: 10.1016/j.molstruc.2016.05.082] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
12 Zeng F, Chen X, Sun K, Zhu H, Yuan X, Liu Y, Qu L, Zhao Y, Yu B. Visible-light-induced metal-free cascade cyclization of N -arylpropiolamides to 3-phosphorylated, trifluoromethylated and thiocyanated azaspiro[4.5]trienones. Org Chem Front 2021;8:760-6. [DOI: 10.1039/d0qo01410a] [Cited by in Crossref: 6] [Cited by in F6Publishing: 1] [Article Influence: 6.0] [Reference Citation Analysis]
13 Ho HE, Stephens TC, Payne TJ, O’brien P, Taylor RJK, Unsworth WP. Merging π-Acid and Pd Catalysis: Dearomatizing Spirocyclization/Cross-Coupling Cascade Reactions of Alkyne-Tethered Aromatics. ACS Catal 2019;9:504-10. [DOI: 10.1021/acscatal.8b03861] [Cited by in Crossref: 31] [Cited by in F6Publishing: 14] [Article Influence: 7.8] [Reference Citation Analysis]
14 Qin Q, Meng T, Tan M, Liu Y, Luo X, Zou B, Liang H. Synthesis and in vitro biological evaluation of three 4′-(4-methoxyphenyl)-2,2′:6′,2″-terpyridine iridium(III) complexes as new telomerase inhibitors. European Journal of Medicinal Chemistry 2018;143:1387-95. [DOI: 10.1016/j.ejmech.2017.10.035] [Cited by in Crossref: 18] [Cited by in F6Publishing: 13] [Article Influence: 4.5] [Reference Citation Analysis]
15 Yu K, Kong X, Yang J, Li G, Xu B, Chen Q. Electrochemical Oxidative Halogenation of N -Aryl Alkynamides for the Synthesis of Spiro[4.5]trienones. J Org Chem 2021;86:917-28. [DOI: 10.1021/acs.joc.0c02429] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
16 Luo L, Jia JJ, Zhong Q, Zhong X, Zheng S, Wang G, He L. Synthesis and anticancer activity evaluation of naphthalene-substituted triazole spirodienones. Eur J Med Chem 2021;213:113039. [PMID: 33261898 DOI: 10.1016/j.ejmech.2020.113039] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
17 Wei W, Cui H, Yang D, Yue H, He C, Zhang Y, Wang H. Visible-light-enabled spirocyclization of alkynes leading to 3-sulfonyl and 3-sulfenyl azaspiro[4,5]trienones. Green Chem 2017;19:5608-13. [DOI: 10.1039/c7gc02330h] [Cited by in Crossref: 101] [Article Influence: 20.2] [Reference Citation Analysis]
18 Ibrahim TS, Hawwas MM, Taher ES, Alhakamy NA, Alfaleh MA, Elagawany M, Elgendy B, Zayed GM, Mohamed MFA, Abdel-Samii ZK, Elshaier YAMM. Design and synthesis of novel pyrazolo[3,4-d]pyrimidin-4-one bearing quinoline scaffold as potent dual PDE5 inhibitors and apoptotic inducers for cancer therapy. Bioorg Chem 2020;105:104352. [PMID: 33080494 DOI: 10.1016/j.bioorg.2020.104352] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
19 Zhou Y, Zhang X, Zhang Y, Ruan L, Zhang J, Zhang-Negrerie D, Du Y. Iodocyclization of N-Arylpropynamides Mediated by Hypervalent Iodine Reagent: Divergent Synthesis of Iodinated Quinolin-2-ones and Spiro[4,5]trienones. Org Lett 2017;19:150-3. [PMID: 28001422 DOI: 10.1021/acs.orglett.6b03455] [Cited by in Crossref: 40] [Cited by in F6Publishing: 27] [Article Influence: 6.7] [Reference Citation Analysis]
20 Chen J, Deng Y, Wang J, Chen S, Peng F, He X, Liu M, Luo H, Zhang J, Chen L. Cyclometalated Ru(II) β-carboline complexes induce cell cycle arrest and apoptosis in human HeLa cervical cancer cells via suppressing ERK and Akt signaling. J Biol Inorg Chem 2021;26:793-808. [PMID: 34459988 DOI: 10.1007/s00775-021-01894-4] [Reference Citation Analysis]
21 Bansode AH, Shaikh SR, Gonnade RG, Patil NT. Intramolecular ipso-arylative cyclization of aryl-alkynoates and N-arylpropiolamides with aryldiazonium salts through merged gold/visible light photoredox catalysis. Chem Commun 2017;53:9081-4. [DOI: 10.1039/c7cc04010e] [Cited by in Crossref: 38] [Cited by in F6Publishing: 2] [Article Influence: 7.6] [Reference Citation Analysis]
22 Nair AM, Halder I, Khan S, Volla CMR. Metal Free Sulfonylative Spirocyclization of Alkenyl and Alkynyl Amides via Insertion of Sulfur Dioxide. Adv Synth Catal 2019;362:224-9. [DOI: 10.1002/adsc.201901321] [Cited by in Crossref: 18] [Cited by in F6Publishing: 9] [Article Influence: 6.0] [Reference Citation Analysis]
23 Qin Q, Wang Z, Wang S, Luo D, Zou B, Yao P, Tan M, Liang H. In vitro and in vivo antitumor activities of three novel binuclear platinum(II) complexes with 4′-substituted-2,2′:6′,2″-terpyridine ligands. European Journal of Medicinal Chemistry 2019;170:195-202. [DOI: 10.1016/j.ejmech.2019.03.014] [Cited by in Crossref: 31] [Cited by in F6Publishing: 19] [Article Influence: 10.3] [Reference Citation Analysis]
24 Chen J, Wang J, Deng Y, Wang T, Miao T, Li C, Cai X, Liu Y, Henri J, Chen L. Ru(II) Complexes Bearing O, O-Chelated Ligands Induced Apoptosis in A549 Cells through the Mitochondrial Apoptotic Pathway. Bioinorg Chem Appl 2020;2020:8890950. [PMID: 32879623 DOI: 10.1155/2020/8890950] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 2.5] [Reference Citation Analysis]
25 Yuan JW, Mou CX, Zhang Y, Hu WY, Yang LR, Xiao YM, Mao P, Zhang SR, Qu LB. Transition-metal catalyzed oxidative spirocyclization of N-aryl alkynamides with methylarenes under microwave irradiation. Org Biomol Chem 2021;19:10348-58. [PMID: 34812461 DOI: 10.1039/d1ob01970h] [Reference Citation Analysis]
26 Ma L, Wang X, Li W, Qu F, Liu Y, Lu J, Su G, Zhao Y. Conjugation of Ginsenoside with Dietary Amino Acids: A Promising Strategy To Suppress Cell Proliferation and Induce Apoptosis in Activated Hepatic Stellate Cells. J Agric Food Chem 2019;67:10245-55. [PMID: 31389238 DOI: 10.1021/acs.jafc.9b03305] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
27 Wan D, Tang B, Wang YJ, Guo BH, Yin H, Yi QY, Liu YJ. Synthesis and anticancer properties of ruthenium (II) complexes as potent apoptosis inducers through mitochondrial disruption. Eur J Med Chem 2017;139:180-90. [PMID: 28800456 DOI: 10.1016/j.ejmech.2017.07.066] [Cited by in Crossref: 60] [Cited by in F6Publishing: 53] [Article Influence: 12.0] [Reference Citation Analysis]
28 Morak-Młodawska B, Pluta K, Latocha M, Suwińska K, Jeleń M, Kuśmierz D. 3,6-Diazaphenothiazines as potential lead molecules - synthesis, characterization and anticancer activity. J Enzyme Inhib Med Chem 2016;31:1512-9. [PMID: 26950280 DOI: 10.3109/14756366.2016.1151014] [Cited by in Crossref: 17] [Cited by in F6Publishing: 13] [Article Influence: 2.8] [Reference Citation Analysis]
29 Hua J, Fang Z, Bian M, Ma T, Yang M, Xu J, Liu C, He W, Zhu N, Yang Z, Guo K. Electrochemical Synthesis of Spiro[4.5]trienones through Radical-Initiated Dearomative Spirocyclization. ChemSusChem 2020;13:2053-9. [PMID: 32012457 DOI: 10.1002/cssc.202000098] [Cited by in Crossref: 16] [Cited by in F6Publishing: 11] [Article Influence: 8.0] [Reference Citation Analysis]
30 Sajadikhah SS, Zahmatkesh S. Synthetic methods for spirofuran-2(5H)-ones (microreview). Chem Heterocycl Comp 2019;55:1165-7. [DOI: 10.1007/s10593-019-02594-3] [Reference Citation Analysis]
31 Yugandhar D, Kuriakose S, Nanubolu JB, Srivastava AK. Synthesis of Alkaloid-Mimicking Tricyclic Skeletons by Diastereo- and Regioselective Ugi/ ipso -Cyclization/Aza-Michael Cascade Reaction in One-Pot. Org Lett 2016;18:1040-3. [DOI: 10.1021/acs.orglett.6b00164] [Cited by in Crossref: 55] [Cited by in F6Publishing: 41] [Article Influence: 9.2] [Reference Citation Analysis]
32 Wu L, Tan F, Li M, Song R, Li J. Fe-Catalyzed oxidative spirocyclization of N-arylpropiolamides with silanes and TBHP involving the formation of C–Si bonds. Org Chem Front 2017;4:350-3. [DOI: 10.1039/c6qo00691d] [Cited by in Crossref: 46] [Article Influence: 9.2] [Reference Citation Analysis]
33 Morak-Młodawska B, Pluta K, Latocha M, Jeleń M, Kuśmierz D, Suwińska K, Shkurenko A, Czuba Z, Jurzak M. 10H-1,9-diazaphenothiazine and its 10-derivatives: synthesis, characterisation and biological evaluation as potential anticancer agents. J Enzyme Inhib Med Chem 2019;34:1298-306. [PMID: 31307242 DOI: 10.1080/14756366.2019.1639695] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]