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For: Liu M, Sun W, Shen L, He Y, Liu J, Wang J, Hu Z, Zhang Y. Bipolarolides A–G: Ophiobolin‐Derived Sesterterpenes with Three New Carbon Skeletons from Bipolaris sp. TJ403‐B1. Angew Chem Int Ed 2019;58:12091-5. [DOI: 10.1002/anie.201905966] [Cited by in Crossref: 35] [Cited by in F6Publishing: 37] [Article Influence: 11.7] [Reference Citation Analysis]
Number Citing Articles
1 Gao W, Jiang R, Zeng H, Cao J, Hu Z, Zhang Y. Armochaetoglasins L and M, new cytochalasans from an arthropod-derived fungus Chaetomium globosum. Natural Product Research 2022. [DOI: 10.1080/14786419.2022.2150846] [Reference Citation Analysis]
2 Zhang P, Qi J, Duan Y, Gao JM, Liu C. Research Progress on Fungal Sesterterpenoids Biosynthesis. J Fungi (Basel) 2022;8:1080. [PMID: 36294645 DOI: 10.3390/jof8101080] [Reference Citation Analysis]
3 Li Y, Zhang L, Wang W, Liu Y, Sun D, Li H, Chen L. A review on natural products with cage-like structure. Bioorg Chem 2022;128:106106. [PMID: 36037599 DOI: 10.1016/j.bioorg.2022.106106] [Reference Citation Analysis]
4 Xiao C, Xu C, Zhang J, Jiang W, Zhang X, Yang C, Xu J, Zhang Y, Zhou T. Soil Microbial Communities Affect the Growth and Secondary Metabolite Accumulation in Bletilla striata (Thunb.) Rchb. f. Front Microbiol 2022;13:916418. [DOI: 10.3389/fmicb.2022.916418] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Jiang T, Dai X, Gao T, Wang L, Yang F, Zhang Y, Wang N, Huang G, Cao J. Ancepsone A, a New Cheilanthane Sesterterpene from Aleuritopteris anceps. Tetrahedron Letters 2022. [DOI: 10.1016/j.tetlet.2022.153869] [Reference Citation Analysis]
6 Lin S, Huang J, Zeng H, Tong Q, Zhang X, Yang B, Ye Y, Wang J, Hu Z, Zhang Y. Distachydrimanes A–F, phenylspirodrimane dimers and hybrids with cytotoxic activity from the coral-derived fungus Stachybotrys chartarum. Chinese Chemical Letters 2022. [DOI: 10.1016/j.cclet.2022.03.064] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Yavari I, Mohsenzadeh R, Ravaghi P. A Molecular Iodine-Mediated Synthesis of Cyclopenta[ c ]furo[3,2- b ]furan-5,6-diones: Assembly of an Angular Dioxatriquinane Core. J Org Chem . [DOI: 10.1021/acs.joc.1c02572] [Reference Citation Analysis]
8 Li K, Chen S, Pang X, Cai J, Zhang X, Liu Y, Zhu Y, Zhou X. Natural products from mangrove sediments-derived microbes: Structural diversity, bioactivities, biosynthesis, and total synthesis. Eur J Med Chem 2022;230:114117. [PMID: 35063731 DOI: 10.1016/j.ejmech.2022.114117] [Cited by in Crossref: 10] [Cited by in F6Publishing: 10] [Article Influence: 10.0] [Reference Citation Analysis]
9 Yan J, Pang J, Liang J, Yu W, Liao X, Aobulikasimu A, Yi X, Yin Y, Deng Z, Hong K. The Biosynthesis and Transport of Ophiobolins in Aspergillus ustus 094102. Int J Mol Sci 2022;23:1903. [PMID: 35163826 DOI: 10.3390/ijms23031903] [Reference Citation Analysis]
10 Lu Y, Chen C, Zhu H, Luo Z, Zhang Y. Highly efficient and fast synthesis of di-iodinated succinimide derivatives from 1,6-enyne and I 2 under air at room temperature. Green Chem . [DOI: 10.1039/d2gc02058k] [Reference Citation Analysis]
11 Liu M, Gu L, Shen L, Zhang X, Lin S, Ye Y, Wang J, Hu Z, Zhang Y. Bipolaquinones A-J, Immunosuppressive Meroterpenoids from a Soil-Derived Bipolaris zeicola. J Nat Prod 2021;84:2427-36. [PMID: 34469134 DOI: 10.1021/acs.jnatprod.1c00327] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 Wei M, Zhou P, Huang L, Yin J, Li Q, Dai C, Wang J, Gu L, Tong Q, Zhu H, Zhang Y. Spectanoids A-H: Eight undescribed sesterterpenoids from Aspergillus spectabilis. Phytochemistry 2021;191:112910. [PMID: 34481345 DOI: 10.1016/j.phytochem.2021.112910] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
13 Yang BY, Sun WG, Liu JJ, Wang JP, Hu ZX, Zhang YH. A new pair of cytotoxic enantiomeric isoprenylated chromone derivatives from Pestalotiopsis sp. J Asian Nat Prod Res 2021;:1-7. [PMID: 34236260 DOI: 10.1080/10286020.2021.1946042] [Reference Citation Analysis]
14 Wang JP, Shu Y, Liu R, Gan JL, Deng SP, Cai XY, Hu JT, Cai L, Ding ZT. Bioactive sesterterpenoids from the fungus Penicillium roqueforti YJ-14. Phytochemistry 2021;187:112762. [PMID: 33940379 DOI: 10.1016/j.phytochem.2021.112762] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
15 Hu Z, Ye Y, Zhang Y. Large-scale culture as a complementary and practical method for discovering natural products with novel skeletons. Nat Prod Rep 2021. [PMID: 33650608 DOI: 10.1039/d0np00069h] [Cited by in Crossref: 10] [Cited by in F6Publishing: 12] [Article Influence: 10.0] [Reference Citation Analysis]
16 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: 3.0] [Reference Citation Analysis]
17 Li K, Gustafson KR. Sesterterpenoids: chemistry, biology, and biosynthesis. Nat Prod Rep 2021;38:1251-81. [PMID: 33350420 DOI: 10.1039/d0np00070a] [Cited by in Crossref: 15] [Cited by in F6Publishing: 18] [Article Influence: 7.5] [Reference Citation Analysis]
18 Li H, Guo J, Zhang R, Wang J, Hu Z, Zhang Y. Two new nucleoside derivatives isolated from the marine-derived Aspergillus versicolor and their intramolecular transesterification. Nat Prod Res 2020;:1-8. [PMID: 33319589 DOI: 10.1080/14786419.2020.1858409] [Reference Citation Analysis]
19 Liu Y, Yu S. Survey of natural products reported by Asian research groups in 2019. Journal of Asian Natural Products Research 2020;22:1101-20. [DOI: 10.1080/10286020.2020.1844675] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
20 Liu M, Zhang X, Shen L, Sun W, Lin S, Liu J, Cao F, Qi C, Wang J, Hu Z, Zhang Y. Bioactive Polyketide-Terpenoid Hybrids from a Soil-Derived Fungus Bipolaris zeicola. J Org Chem 2021;86:10962-74. [DOI: 10.1021/acs.joc.0c02237] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
21 Jeon H, Winkler JD. Synthesis of Cyclohexane-Angularly-Fused Triquinanes. Synthesis (Stuttg) 2021;53:475-88. [PMID: 34334830 DOI: 10.1055/s-0040-1705953] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
22 Lin S, Zhang X, Shen L, Mo S, Liu J, Wang J, Hu Z, Zhang Y. A new abietane-type diterpenoid and a new long-chain alkenone from fungus Daldinia sp. TJ403-LS1. Nat Prod Res 2020;:1-8. [PMID: 32643425 DOI: 10.1080/14786419.2020.1789638] [Reference Citation Analysis]
23 Li H, Zhang R, Cao F, Wang J, Hu Z, Zhang Y. Proversilins A-E, Drimane-Type Sesquiterpenoids from the Endophytic Aspergillus versicolor. J Nat Prod 2020;83:2200-6. [PMID: 32628478 DOI: 10.1021/acs.jnatprod.0c00298] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 5.5] [Reference Citation Analysis]
24 Zimnitskiy NS, Denikaev AD, Barkov AY, Kutyashev IB, Korotaev VY, Sosnovskikh VY. Catalyst-free Tandem 1,3-Dipolar Cycloaddition/Aldol Condensation: Diastereoselective Construction of the Azatetraquinane Skeleton. J Org Chem 2020;85:8683-94. [PMID: 32517470 DOI: 10.1021/acs.joc.0c01127] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 3.5] [Reference Citation Analysis]
25 Lin S, He Y, Li F, Yang B, Liu M, Zhang S, Liu J, Li H, Qi C, Wang J, Hu Z, Zhang Y. Structurally diverse and bioactive alkaloids from an insect-derived fungus Neosartorya fischeri. Phytochemistry 2020;175:112374. [DOI: 10.1016/j.phytochem.2020.112374] [Cited by in Crossref: 5] [Cited by in F6Publishing: 7] [Article Influence: 2.5] [Reference Citation Analysis]
26 Shen L, Liu M, He Y, Al Anbari WH, Li H, Lin S, Chai C, Wang J, Hu Z, Zhang Y. Novel Antimicrobial Compounds as Ophiobolin-Type Sesterterpenes and Pimarane-Type Diterpene From Bipolaris Species TJ403-B1. Front Microbiol 2020;11:856. [PMID: 32547498 DOI: 10.3389/fmicb.2020.00856] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 3.0] [Reference Citation Analysis]
27 Li F, Lin S, Zhang S, Pan L, Chai C, Su J, Yang B, Liu J, Wang J, Hu Z, Zhang Y. Modified Fusicoccane-Type Diterpenoids from Alternaria brassicicola. J Nat Prod 2020;83:1931-8. [DOI: 10.1021/acs.jnatprod.0c00165] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 5.5] [Reference Citation Analysis]
28 Peng C, Arya P, Zhou Z, Snyder SA. A Concise Total Synthesis of (+)‐Waihoensene Guided by Quaternary Center Analysis. Angew Chem 2020;132:13623-7. [DOI: 10.1002/ange.202004177] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
29 Wu Q, Li SW, Xu H, Wang H, Hu P, Zhang H, Luo C, Chen KX, Nay B, Guo YW, Li XW. Complex Polypropionates from a South China Sea Photosynthetic Mollusk: Isolation and Biomimetic Synthesis Highlighting Novel Rearrangements. Angew Chem Int Ed Engl 2020;59:12105-12. [PMID: 32277730 DOI: 10.1002/anie.202003643] [Cited by in Crossref: 36] [Cited by in F6Publishing: 38] [Article Influence: 18.0] [Reference Citation Analysis]
30 Wu Q, Li S, Xu H, Wang H, Hu P, Zhang H, Luo C, Chen K, Nay B, Guo Y, Li X. Complex Polypropionates from a South China Sea Photosynthetic Mollusk: Isolation and Biomimetic Synthesis Highlighting Novel Rearrangements. Angew Chem 2020;132:12203-10. [DOI: 10.1002/ange.202003643] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 4.5] [Reference Citation Analysis]
31 Liu MT, He Y, Shen L, Hu ZX, Zhang YH. Bipolarins A-H, eight new ophiobolin-type sesterterpenes with antimicrobial activity from fungus Bipolaris sp. TJ403-B1. Chin J Nat Med 2019;17:935-44. [PMID: 31882049 DOI: 10.1016/S1875-5364(19)30116-5] [Cited by in Crossref: 8] [Cited by in F6Publishing: 12] [Article Influence: 4.0] [Reference Citation Analysis]
32 Lin S, Yu H, Yang B, Li F, Chen X, Li H, Zhang S, Wang J, Hu Y, Hu Z, Zhang Y. Reisolation and Configurational Reinvestigation of Cottoquinazolines E–G from an Arthropod-Derived Strain of the Fungus Neosartorya fischeri. J Nat Prod 2020;83:169-73. [DOI: 10.1021/acs.jnatprod.9b01000] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 3.0] [Reference Citation Analysis]
33 Wang J, Shu Y, Hu J, Liu R, Cai X, Sun C, Gan D, Zhou D, Mei R, Ding H, Zhang X, Cai L, Ding Z. Roquefornine A, a sesterterpenoid with a 5/6/5/5/6-fused ring system from the fungus Penicillium roqueforti YJ-14. Org Chem Front 2020;7:1463-8. [DOI: 10.1039/d0qo00301h] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 5.5] [Reference Citation Analysis]
34 Gao W, Chai C, He Y, Li F, Hao X, Cao F, Gu L, Liu J, Hu Z, Zhang Y. Periconiastone A, an Antibacterial Ergosterol with a Pentacyclo[8.7.0.0 1,5 .0 2,14 .0 10,15 ]heptadecane System from Periconia sp. TJ403-rc01. Org Lett 2019;21:8469-72. [DOI: 10.1021/acs.orglett.9b03270] [Cited by in Crossref: 34] [Cited by in F6Publishing: 34] [Article Influence: 11.3] [Reference Citation Analysis]
35 Liu M, Sun W, Shen L, Hao X, Al Anbari WH, Lin S, Li H, Gao W, Wang J, Hu Z, Zhang Y. Bipolaricins A–I, Ophiobolin-Type Tetracyclic Sesterterpenes from a Phytopathogenic Bipolaris sp. Fungus. J Nat Prod 2019;82:2897-906. [DOI: 10.1021/acs.jnatprod.9b00744] [Cited by in Crossref: 13] [Cited by in F6Publishing: 15] [Article Influence: 4.3] [Reference Citation Analysis]
36 Hill RA, Sutherland A. Hot off the press. Nat Prod Rep 2019;36:1378-82. [DOI: 10.1039/c9np90041a] [Reference Citation Analysis]