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For: Marcarino MO, Cicetti S, Zanardi MM, Sarotti AM. A critical review on the use of DP4+ in the structural elucidation of natural products: the good, the bad and the ugly. A practical guide. Nat Prod Rep 2021. [PMID: 34212963 DOI: 10.1039/d1np00030f] [Cited by in Crossref: 23] [Cited by in F6Publishing: 27] [Article Influence: 11.5] [Reference Citation Analysis]
Number Citing Articles
1 Zhao J, Yue J. Frontier studies on natural products: moving toward paradigm shifts. Sci China Chem 2023. [DOI: 10.1007/s11426-022-1512-0] [Reference Citation Analysis]
2 Cortés I, Cuadrado C, Hernández Daranas A, Sarotti AM. Machine learning in computational NMR-aided structural elucidation. Front Nat Produc 2023;2. [DOI: 10.3389/fntpr.2023.1122426] [Reference Citation Analysis]
3 Böselt L, Aerts R, Herrebout W, Riniker S. Improving the IR spectra alignment algorithm with spectra deconvolution and combination with Raman or VCD spectroscopy. Phys Chem Chem Phys 2023;25:2063-74. [PMID: 36546852 DOI: 10.1039/d2cp04907d] [Reference Citation Analysis]
4 Chao CH, Wu YJ, Huang TY, Tai CJ, Chen YJ, Huang CY, Lin CC, Dai CF, Huang HC, Sheu JH. Isosarcophytoxide Derivatives with a 2,5-Dihydrofuran Moiety from the Soft Coral Sarcophyton cinereum. Molecules 2023;28:641. [PMID: 36677699 DOI: 10.3390/molecules28020641] [Reference Citation Analysis]
5 Le NT, Vermeyen T, Aerts R, Herrebout WA, Pieters L, Tuenter E. Epimeric Mixture Analysis and Absolute Configuration Determination Using an Integrated Spectroscopic and Computational Approach-A Case Study of Two Epimers of 6-Hydroxyhippeastidine. Molecules 2022;28. [PMID: 36615407 DOI: 10.3390/molecules28010214] [Reference Citation Analysis]
6 Zhong W, Li M, Gu R, Ding R, Cao L, Mu Z, Du X, Feng Y, Wei R, Zhan L, Zhong G. Lipskynoids A-G, New Acyclic Diterpenes from the Flowers of Carpesium lipskyi. Chem Biodivers 2022;19:e202200898. [PMID: 36239633 DOI: 10.1002/cbdv.202200898] [Reference Citation Analysis]
7 Wang Q, Chen H, Wu K, Li X, Liu J. Antibacterial and β-amyloid precursor protein-cleaving enzyme 1 inhibitory polyketides from the fungus Aspergillus chevalieri. Front Microbiol 2022;13. [DOI: 10.3389/fmicb.2022.1051281] [Reference Citation Analysis]
8 Shi H, Jiang J, Zhang H, Jiang H, Su Z, Liu D, Jie L, He F. Antibacterial spirooxindole alkaloids from Penicillium brefeldianum inhibit dimorphism of pathogenic smut fungi. Front Microbiol 2022;13. [DOI: 10.3389/fmicb.2022.1046099] [Reference Citation Analysis]
9 Lin Y, Chao C, Fu C, Chiou S, Huang T, Yang Y, Wu S, Chen S, Wang H, Yu M, Huang H, Sheu J. Computationally assisted structure elucidation of new 2-guanidinoethanesulfonyl sesquiterpenoid alkaloids: Agelasidines G–I from the marine sponge Agelas nakamurai. Tetrahedron 2022;126:133077. [DOI: 10.1016/j.tet.2022.133077] [Reference Citation Analysis]
10 Feng Z, Huang P, Jiang S, Shen S, Chen J. Three new highly oxygenated azaphilones from an endophytic fungus Penicillium sp. LZUC-S1. Tetrahedron Letters 2022. [DOI: 10.1016/j.tetlet.2022.154260] [Reference Citation Analysis]
11 Li Q, Yang S, Teng H, Li X, Xie W, Wu Z, Yang G, Xu J, Chen Y. Structural elucidation of two intricate polycyclic polyprenylated acylphloroglucinols using quantum chemical calculations and their hypoglycemic activities. Arabian Journal of Chemistry 2022;15:104137. [DOI: 10.1016/j.arabjc.2022.104137] [Reference Citation Analysis]
12 Lu YB, Luo S, Wang YX, Feng ZY, Gao K, Chen JJ. Jatrophane diterpenoids with cytotoxic activity from the whole plant of Euphorbia heliosocpia L. Phytochemistry 2022;:113420. [PMID: 36055424 DOI: 10.1016/j.phytochem.2022.113420] [Reference Citation Analysis]
13 Duan Y, Bu P, Guo Y, Shi Z, Cao Y, Zhang Y, Hu H, Hu H, Qi C, Zhang Y. (±)-Walskiiglucinol A, a pair of rearranged acylphloroglucinol derivative enantiomers from Hypericum przewalskii. Org Biomol Chem 2022;20:4970-5. [PMID: 35674501 DOI: 10.1039/d2ob00562j] [Reference Citation Analysis]
14 Li A, Ma X, Zhang R, Jiao S, Li W, Gao X, Xu J, Tu P, Chai X. Syringenes M - Q, Eremophilane Sesquiterpenoid Dimers from the Peeled Stems of Syringa pinnatifolia. Chem Biodivers 2022;:e202200245. [PMID: 35652443 DOI: 10.1002/cbdv.202200245] [Reference Citation Analysis]
15 Hu Y, Saito Y, Matsuo Y, Gong X, Tanaka T. Two new dimeric benzofuran diastereomers from the roots of Eupatorium heterophyllum. Tetrahedron Letters 2022. [DOI: 10.1016/j.tetlet.2022.153924] [Reference Citation Analysis]
16 Zhang Y, Xia GY, Wu YZ, Wei XH, Xia H, Wang LY, Lin PC, Wang YN, Chen LX, Lin S. Two New Nor-seco-Isodhilarane-Type Meroterpenoids from the Endophytic Fungus Penicillium purpurogenum. Chem Biodivers 2022;:e202200403. [PMID: 35596060 DOI: 10.1002/cbdv.202200403] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
17 Huo Z, Zhu F, Zhang X, Zhang X, Liang H, Yao J, Liu Z, Zhang G, Yao Q, Qin G. Approaches to Configuration Determinations of Flexible Marine Natural Products: Advances and Prospects. Marine Drugs 2022;20:333. [DOI: 10.3390/md20050333] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
18 Wang H, Ma G, Wang H, Li L, Dong A, Liu H, Huo X, Si J, Wang J. Novel Triterpenoid Alkaloids With Their Potential Cytotoxic Activity From the Roots of Siraitia grosvenorii. Front Chem 2022;10:885487. [DOI: 10.3389/fchem.2022.885487] [Reference Citation Analysis]
19 Hong X, Guan X, Lai Q, Yu D, Chen Z, Fu X, Zhang B, Chen C, Shao Z, Xia J, Qin JJ, Wang W. Characterization of a bioactive meroterpenoid isolated from the marine-derived fungus Talaromyces sp. Appl Microbiol Biotechnol 2022. [PMID: 35416486 DOI: 10.1007/s00253-022-11914-1] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
20 Li J, Tan Y, Liu S, Wu X, Wang J, Xu K, Tan G, Zou Z, Wang W. Reassignment of the structures of pestalopyrones A–D. Phytochemistry 2022. [DOI: 10.1016/j.phytochem.2022.113205] [Reference Citation Analysis]
21 Zaman KAU, Wu X, Sarotti AM, Cao S. New and bioactive polyketides from Hawaiian marine-derived fungus Trichoderma sp. FM652. Nat Prod Res 2022;:1-7. [PMID: 35337234 DOI: 10.1080/14786419.2022.2056890] [Reference Citation Analysis]
22 Zhao WY, Sun CP, Chang YB, Wang WY, Yan JK, Lv X, Wang C, Ma XC. Unprecedented diterpenoid dimers with soluble epoxide hydrolase inhibitory effect from Euphorbia fischeriana. Org Biomol Chem 2022;20:2508-17. [PMID: 35266497 DOI: 10.1039/d2ob00053a] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
23 Boudermine S, Parisi V, Lemoui R, Boudiar T, Chini MG, Franceschelli S, Pecoraro M, Pascale M, Bifulco G, Braca A, De Tommasi N, De Leo M. Cytotoxic Sesquiterpenoids from Ammoides atlantica Aerial Parts. J Nat Prod 2022. [PMID: 35196017 DOI: 10.1021/acs.jnatprod.1c01211] [Reference Citation Analysis]
24 Wu YZ, Xia GY, Xia H, Wang LY, Wang YN, Li L, Shang HC, Lin S. Seco and Nor-seco Isodhilarane-Type Meroterpenoids from Penicillium purpurogenum and the Configuration Revisions of Related Compounds. J Nat Prod 2022. [PMID: 34978193 DOI: 10.1021/acs.jnatprod.1c01025] [Cited by in Crossref: 3] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
25 Wang Y, Chintalapudi V, Gudmundsson HG, Challis GL, Anderson EA. Synthesis of the C50 diastereomers of the C33–C51 fragment of stambomycin D. Org Chem Front 2022;9:445-9. [DOI: 10.1039/d1qo01635k] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
26 Groleau RR, Powell ME, Evans CD, Fordred PS, Bull SD, James TD. Diastereomeric Derivatization for Spectroscopy. Reference Module in Chemistry, Molecular Sciences and Chemical Engineering 2022. [DOI: 10.1016/b978-0-32-390644-9.00010-x] [Reference Citation Analysis]
27 Qiao Y, Tan X, Xu Q, Zhang Z, Xu Q, Tao L, Liu J, Zhu H, Chen C, Ye Y, Lu Y, Chen G, Qi C, Zhang Y. Asperosin A, a [4 + 2] Diels–Alder cycloaddition polyketide dimer from Aspergillus rugulosa with immunosuppressive activity. Org Chem Front 2022;9:2477-85. [DOI: 10.1039/d1qo01767e] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
28 Novitskiy IM, Kutateladze AG. DU8+ Computations Reveal a Common Challenge in the Structure Assignment of Natural Products Containing a Carboxylic Anhydride Moiety. J Org Chem 2021;86:17511-5. [PMID: 34743508 DOI: 10.1021/acs.joc.1c02291] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
29 Lim J, Chintalapudi V, Gudmundsson HG, Tran M, Bernasconi A, Blanco A, Song L, Challis GL, Anderson EA. Synthesis of the C1-C27 Fragment of Stambomycin D Validates Modular Polyketide Synthase-Based Stereochemical Assignments. Org Lett 2021;23:7439-44. [PMID: 34494848 DOI: 10.1021/acs.orglett.1c02650] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
30 Yang B, Huang J, Lin S, Tong Q, Yao Z, Li F, Ye Y, Hu Z, Zhang Y. Hyperbeanone A, a 5,6- seco -spirocyclic polycyclic polyprenylated acylphloroglucinol derivative with an unprecedented skeleton from Hypericum beanii. Org Chem Front 2021;8:6411-8. [DOI: 10.1039/d1qo01302e] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]