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For: Shang XF, Yang CJ, Morris-Natschke SL, Li JC, Yin XD, Liu YQ, Guo X, Peng JW, Goto M, Zhang JY, Lee KH. Biologically active isoquinoline alkaloids covering 2014-2018. Med Res Rev 2020;40:2212-89. [PMID: 32729169 DOI: 10.1002/med.21703] [Cited by in Crossref: 43] [Cited by in F6Publishing: 43] [Article Influence: 21.5] [Reference Citation Analysis]
Number Citing Articles
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16 Du K, Liu Y, Zong K, Wang Y, Li J, Meng D. Isoquinoline alkaloids from the Corydalis tomentella with potential anti-hepatoma and antibacterial activities. Phytochemistry 2022;:113240. [PMID: 35597315 DOI: 10.1016/j.phytochem.2022.113240] [Reference Citation Analysis]
17 Chen Y, Hamidu S, Yang X, Yan Y, Wang Q, Li L, Oduro PK, Li Y. Dietary Supplements and Natural Products: An Update on Their Clinical Effectiveness and Molecular Mechanisms of Action During Accelerated Biological Aging. Front Genet 2022;13:880421. [PMID: 35571015 DOI: 10.3389/fgene.2022.880421] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
18 Wang K, Li Y, Zhang W, Chen R, Ma X, Wang M, Zhou N. Facile Synthesis of Tricyclic 1,2,4-Oxadiazolines-Fused Tetrahydro-Isoquinolines from Oxime Chlorides with 3,4-Dihydroisoquinoline Imines. Molecules 2022;27:3064. [PMID: 35630538 DOI: 10.3390/molecules27103064] [Reference Citation Analysis]
19 Nova-Fernández JL, García MJ, Mollari L, Pascual-Coca G, Cabrera S, Alemán J. Continuous-flow synthesis of alkyl zinc sulfinates for the direct photofunctionalization of heterocycles. Chem Commun (Camb) 2022;58:4611-4. [PMID: 35315862 DOI: 10.1039/d2cc01065h] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
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22 Muthusamy S, Kumarswamyreddy N, Kesavan V. Enantioselective Synthesis of 3‐Amino‐3’‐carbazole Oxindole Derivatives via Friedel‐Crafts Aminoalkylation Reaction. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202200131] [Reference Citation Analysis]
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24 Yu JH, Yu ZP, Capon RJ, Zhang H. Natural Enantiomers: Occurrence, Biogenesis and Biological Properties. Molecules 2022;27:1279. [PMID: 35209066 DOI: 10.3390/molecules27041279] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]
25 Sun PT, Cao YG, Xue GM, Li M, Zhang CL, Zhao F, Cao ZY, Wang D, Gustafson KR, Zheng XK, Feng WS, Chen H. Hypeisoxazole A, a Racemic Pair of Tetrahydroisoxazole-Fused Benzylisoquinoline Alkaloids from Hypecoum erectum and Structural Revision of Hypecoleptopine. Org Lett 2022. [PMID: 35147434 DOI: 10.1021/acs.orglett.2c00096] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
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27 Lu Q, Li R, Yang Y, Zhang Y, Zhao Q, Li J. Ingredients with anti-inflammatory effect from medicine food homology plants. Food Chem 2022;368:130610. [PMID: 34419798 DOI: 10.1016/j.foodchem.2021.130610] [Cited by in Crossref: 10] [Cited by in F6Publishing: 7] [Article Influence: 10.0] [Reference Citation Analysis]
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31 Stepanova VA, Patrushev SS, Rybalova TV, Shults EE. Cross-copling reaction to access a library of eudesmane-type methylene lactones with quinoline or isoquinoline substituent. Journal of Molecular Structure 2022;1247:131373. [DOI: 10.1016/j.molstruc.2021.131373] [Reference Citation Analysis]
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