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For: Hou W, Xu H. Incorporating Selenium into Heterocycles and Natural Products─From Chemical Properties to Pharmacological Activities. J Med Chem 2022. [PMID: 35244394 DOI: 10.1021/acs.jmedchem.1c01859] [Cited by in Crossref: 12] [Cited by in F6Publishing: 17] [Article Influence: 12.0] [Reference Citation Analysis]
Number Citing Articles
1 Huang HY, Wang Q, Zhang CY, Chen ZX, Wang JT, Liao XW, Yu RJ, Xiong YS. Synthesis and biological evaluation of ruthenium complexes containing phenylseleny against Gram-positive bacterial infection by damage membrane integrity and avoid drug-resistance. J Inorg Biochem 2023;242:112175. [PMID: 36898296 DOI: 10.1016/j.jinorgbio.2023.112175] [Reference Citation Analysis]
2 Liu L, Wen C, Sun G, Li Y, Zhang J, Zhang Z, Wang Z, She M, Liu P, Zhang S, Li J. Multisite-Sequential Cyclization To Construct 1,2,4-Triazole-Based N-Fused Heterocyclics. Org Lett 2023;25:1530-5. [PMID: 36852941 DOI: 10.1021/acs.orglett.3c00322] [Reference Citation Analysis]
3 Huang YM, Cheng Y, Peng ZN, Pang LP, Li JY, Xiao JA, Zhang YF, Cui JG. Synthesis and antitumor activity of some cholesterol-based selenocyanate compounds. Steroids 2023;:109217. [PMID: 36893827 DOI: 10.1016/j.steroids.2023.109217] [Reference Citation Analysis]
4 Sun W, Zhou L, Liu G, Zheng Y, Song J, Zou H. Enhanced electro-Fenton degradation of sulfamethazine using Co-based selenite modified graphite cathode via in-situ generation of •OH. Chemical Engineering Journal 2023. [DOI: 10.1016/j.cej.2023.142419] [Reference Citation Analysis]
5 Shagufta, Ahmad I. Therapeutic significance of molecular hybrids for breast cancer research and treatment. RSC Med Chem 2023;14:218-38. [PMID: 36846377 DOI: 10.1039/d2md00356b] [Reference Citation Analysis]
6 Wang Q, Xiao F, Huang Z, Mao G, Deng GJ. CuBr(2)-Catalyzed Annulation of 2-Bromo-N-Arylbenzimidamide with Se/S(8) Powder for the Synthesis of Benzo[d]isoselenazole and Benzo[d]isothiazole. J Org Chem 2023;88:1963-76. [PMID: 36720013 DOI: 10.1021/acs.joc.2c02088] [Reference Citation Analysis]
7 Hu J, Chen L, Lu Z, Yao H, Hu Y, Feng L, Pang Y, Wu JQ, Yu Z, Chen WH. Design, Synthesis and Antitumor Activity of Novel Selenium-Containing Tepotinib Derivatives as Dual Inhibitors of c-Met and TrxR. Molecules 2023;28:1304. [PMID: 36770971 DOI: 10.3390/molecules28031304] [Reference Citation Analysis]
8 Zhou P, Jiao H, Niu K, Song H, Liu Y, Wang Q. Facile and General Electrochemical Diselenylation of Terminal Alkynes. ACS Sustainable Chem Eng 2023. [DOI: 10.1021/acssuschemeng.2c06864] [Reference Citation Analysis]
9 Deeksha, Sathish E, Kiran, Singh R. Access to Sterically Hindered Thioethers (α-Thioamides) Under Mild Conditions Using α-Halohydroxamates: Application toward 1,4-Benzothiazinones and 4,1-Benzothiazepinones. J Org Chem 2023;88:901-8. [PMID: 36576371 DOI: 10.1021/acs.joc.2c02274] [Reference Citation Analysis]
10 Wei G, Zhang J, Wang H, Chen Z, Wu XF. Radical selenylative cyclization of trifluoromethyl propargyl imines for the synthesis of trifluoromethyl- and seleno-azaspiro[4,5]-tetraenones and quinolines. Org Biomol Chem 2023;21:284-8. [PMID: 36484764 DOI: 10.1039/d2ob02033e] [Reference Citation Analysis]
11 Kakakhan C, Türkeş C, Güleç Ö, Demir Y, Arslan M, Özkemahlı G, Beydemir Ş. Exploration of 1,2,3-triazole linked benzenesulfonamide derivatives as isoform selective inhibitors of human carbonic anhydrase. Bioorg Med Chem 2023;77:117111. [PMID: 36463726 DOI: 10.1016/j.bmc.2022.117111] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 5.0] [Reference Citation Analysis]
12 Xu-xu Q, Nishii Y, Miura M. Synthesis of Diarylselenides through Rh-Catalyzed Direct Diarylation of Elemental Selenium with Benzamides. J Org Chem 2022. [DOI: 10.1021/acs.joc.2c02131] [Reference Citation Analysis]
13 Ramos-inza S, Plano D, Sanmartín C. Metal-based compounds containing selenium: An appealing approach towards novel therapeutic drugs with anticancer and antimicrobial effects. European Journal of Medicinal Chemistry 2022;244:114834. [DOI: 10.1016/j.ejmech.2022.114834] [Reference Citation Analysis]
14 Goulart HA, Araujo DR, Barcellos AM, Jacob RG, Lenardão EJ, Perin G. One‐pot Sequential Strategy to Prepare Organoselanyl and Organotellanyl Isoquinolinium Imides. Eur J Org Chem 2022;2022. [DOI: 10.1002/ejoc.202201027] [Reference Citation Analysis]
15 Jiang Y, Wang Y, Zhou C, Zhang Y, Ling Y, Zhao Y, Liu G. N-Fluorobenzenesulfonimide-Mediated Intermolecular Carboselenenylation of Olefins with Aromatics and Diselenides. J Org Chem 2022. [DOI: 10.1021/acs.joc.2c01989] [Reference Citation Analysis]
16 Zhang X, Zuo T, Yu L. Ag/Se‐Catalyzed Selective Epoxidation of β ‐Ionone with Molecular Oxygen. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202203514] [Reference Citation Analysis]
17 do Carmo Pinheiro R, Back DF, Müller SG, Nogueira CW, Zeni G. Potassium tert -Butoxide-Promoted Tandem Cyclization of Organoselenium Alkynyl Aryl Propargyl Ethers. J Org Chem . [DOI: 10.1021/acs.joc.2c01598] [Reference Citation Analysis]
18 Shi Z, Liu J, Tian L, Li J, Gao Y, Xing Y, Yan W, Hua C, Xie X, Liu C, Liang C. Insights into stimuli-responsive diselenide bonds utilized in drug delivery systems for cancer therapy. Biomed Pharmacother 2022;155:113707. [PMID: 36122520 DOI: 10.1016/j.biopha.2022.113707] [Reference Citation Analysis]
19 Feng X, Pan L, Qian Z, Liu D, Guan X, Feng L, Song B, Xu X, Tan N, Ma Y, Li Z, Wang Z, Bian J. Discovery of Selenium-Containing STING Agonists as Orally Available Antitumor Agents. J Med Chem 2022. [PMID: 36069713 DOI: 10.1021/acs.jmedchem.2c00634] [Reference Citation Analysis]
20 Sun SS, Mo ZY, Chen YY, Xu YL. Synthesis of Selenyl-Substituted Quinoline Derivatives via Substrate-Controlled Three-Component Domino Reactions. J Org Chem 2022. [PMID: 36048432 DOI: 10.1021/acs.joc.2c01260] [Reference Citation Analysis]
21 Xu H, Wang Y, Dong H, Zhang Y, Gu Y, Zhang S, Meng Y, Li J, Shi XJ, Ji Q, Liu L, Ma P, Ma F, Yang G, Hou W. Selenylation Chemistry Suitable for On‐Plate Parallel and On‐DNA Library Synthesis Enabling High‐Throughput Medicinal Chemistry. Angew Chem Int Ed 2022;61. [DOI: 10.1002/anie.202206516] [Reference Citation Analysis]
22 Xu H, Wang Y, Dong H, Zhang Y, Gu Y, Zhang S, Meng Y, Li J, Shi XJ, Ji Q, Liu L, Ma P, Ma F, Yang G, Hou W. Selenylation Chemistry Suitable for On‐Plate Parallel and On‐DNA Library Synthesis Enabling High‐Throughput Medicinal Chemistry. Angewandte Chemie. [DOI: 10.1002/ange.202206516] [Reference Citation Analysis]
23 Auld N, Flood K, Kesharwani T, Cavnar PJ. A study on the cellular and cytotoxic effects of S and Se heterocycles on the myeloid leukemia cell line PLB-985. Phosphorus, Sulfur, and Silicon and the Related Elements. [DOI: 10.1080/10426507.2022.2085272] [Reference Citation Analysis]
24 Rubio-Hernández M, Alcolea V, Pérez-Silanes S. Potential of sulfur-selenium isosteric replacement as a strategy for the development of new anti-chagasic drugs. Acta Trop 2022;233:106547. [PMID: 35667455 DOI: 10.1016/j.actatropica.2022.106547] [Reference Citation Analysis]
25 Deng X, Xie B, Li Q, Xiao Y, Hu Z, Deng X, Fang P, Dong C, Zhou HB, Huang J. Discovery of Novel Bicyclic Phenylselenyl-Containing Hybrids: An Orally Bioavailable, Potential, and Multiacting Class of Estrogen Receptor Modulators against Endocrine-Resistant Breast Cancer. J Med Chem 2022. [PMID: 35611405 DOI: 10.1021/acs.jmedchem.2c00525] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
26 Bartz RH, Silva KB, Peglow TJ, Barcellos AM, Jacob RG, Lenardão EJ, Perin G. Radical cyclization of alkynyl aryl ketones for the synthesis of 3-seleno-substituted thiochromones and chromones. Org Biomol Chem 2022. [DOI: 10.1039/d2ob01762h] [Reference Citation Analysis]