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For: Wang FP, Chen QH, Liu XY. Diterpenoid alkaloids. Nat Prod Rep 2010;27:529-70. [PMID: 20336236 DOI: 10.1039/b916679c] [Cited by in Crossref: 236] [Cited by in F6Publishing: 237] [Article Influence: 18.2] [Reference Citation Analysis]
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9 Cui H, Chen X, Chen X, He J, Zhu L, Liu Z, Zhao Z. Diterpenoids with anti-inflammatory activity from the lateral root of Aconitum carmichaelii debeaux. Phytochemistry 2022;204:113455. [PMID: 36174719 DOI: 10.1016/j.phytochem.2022.113455] [Reference Citation Analysis]
10 Yan Y, Jiang H, Yang X, Ding Z, Yin T. Grandiflolines A–F, new anti-inflammatory diterpenoid alkaloids isolated from Delphinium grandiflorum. Front Chem 2022;10:1012874. [DOI: 10.3389/fchem.2022.1012874] [Reference Citation Analysis]
11 Jin S, Zhao X, Ma D. Divergent Total Syntheses of Napelline-Type C20-Diterpenoid Alkaloids: (-)-Napelline, (+)-Dehydronapelline, (-)-Songorine, (-)-Songoramine, (-)-Acoapetaldine D, and (-)-Liangshanone. J Am Chem Soc 2022. [PMID: 35948501 DOI: 10.1021/jacs.2c06738] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
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13 Ding H, Wang JP, Deng SP, Gan JL, Li BX, Yao LL, Zhang SQ, Cai L, Ding ZT. A new sesquiterpenoid from the aconitum-derived fungus Aspergillus fumigatus M1. Nat Prod Res 2022;:1-9. [PMID: 35609146 DOI: 10.1080/14786419.2022.2080207] [Reference Citation Analysis]
14 Zhang J, Lei X, Wei Y, Liu H, Guo Q, Zhang T, Shi J. Two unique C21-diterpenoid alkaloids from Aconitum carmichaelii. Chinese Chemical Letters 2022. [DOI: 10.1016/j.cclet.2022.03.104] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
15 Wang Y, Tao P, Wang Y. Attenuated Structural Transformation of Indaconitine during Sand Frying Process and Anti-Arrhythmic Effects of Its Transformed Products. Evidence-Based Complementary and Alternative Medicine 2022;2022:1-12. [DOI: 10.1155/2022/8606459] [Reference Citation Analysis]
16 Li J, Li X, Gao F, Cai L, Liang X, Chen L, Zhou X. Five new diterpenoid alkaloids from Aconitum sczukinii Turcz. Phytochemistry Letters 2022;47:120-4. [DOI: 10.1016/j.phytol.2021.12.003] [Reference Citation Analysis]
17 Huang S, Feng Y, Ren J, Yang C, Chen L, Zhou X. Diterpenoid Alkaloids from the Roots of Aconitum rockii and Their Antifeedant Activity. Chinese Journal of Organic Chemistry 2022;42:1856. [DOI: 10.6023/cjoc202111006] [Reference Citation Analysis]
18 Yan Y, Li X, Wang Z, Yang X, Yin T. C18-diterpenoid alkaloids in tribe Delphineae (Ranunculaceae): phytochemistry, chemotaxonomy, and bioactivities. RSC Adv 2021;12:395-405. [PMID: 35424499 DOI: 10.1039/d1ra08132b] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
19 Umekubo N, Taniguchi T, Monde K, Hayashi Y. Synthesis of Bicyclo[2.2.2]octanes with a Quaternary Bridgehead Carbon by Diphenylprolinol Silyl Ether‐mediated Domino Reaction. Asian J Org Chem 2021;10:3261-3265. [DOI: 10.1002/ajoc.202100573] [Reference Citation Analysis]
20 Tsyrlina EM, Gabbasov TM, Spirikhin LV, Yunusov MS. New C-19-Substituted Lappaconitine Derivatives. Chem Nat Compd 2021;57:1066-73. [DOI: 10.1007/s10600-021-03551-3] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
21 Kato R, Saito H, Uda S, Domon D, Ikeuchi K, Suzuki T, Tanino K. Synthesis of Seven-Membered Cross-Conjugated Cyclic Trienes by 8π Electrocyclic Reaction. Org Lett 2021;23:8878-82. [PMID: 34714079 DOI: 10.1021/acs.orglett.1c03383] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
22 Yin T, Zhang H, Zhang W, Jiang Z. Chemistry and biological activities of hetisine-type diterpenoid alkaloids. RSC Adv 2021;11:36023-33. [PMID: 35492752 DOI: 10.1039/d1ra07173d] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
23 Song Z, Gao C, Jiang Q, Xu J, Xiong L, Liu K, Sun D, Li H, Chen L. Diterpenoid alkaloids from Delphinium forrestii var. viride and their anti-inflammation activity. Phytochemistry 2021;192:112971. [PMID: 34628107 DOI: 10.1016/j.phytochem.2021.112971] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
24 Cheremnykh KP, Savelyev VA, Shults EE. An Efficient Access to 3,5‐Disubstituted Isoxazoles with Anthranilate Ester Moiety: Alkaloid Lappaconitine – Aryl Conjugates with an Isoxazole Linker. Asian J of Organic Chemis 2021;10:2638-2643. [DOI: 10.1002/ajoc.202100474] [Reference Citation Analysis]
25 Nay B. Total Synthesis of Poisonous Aconitum Alkaloids Empowered by a Fragment Coupling Strategy. ACS Cent Sci 2021;7:1298-9. [PMID: 34471674 DOI: 10.1021/acscentsci.1c00887] [Reference Citation Analysis]
26 Shen Y, Liang WJ, Shi YN, Kennelly EJ, Zhao DK. Structural diversity, bioactivities, and biosynthesis of natural diterpenoid alkaloids. Nat Prod Rep 2020;37:763-96. [PMID: 32129397 DOI: 10.1039/d0np00002g] [Cited by in Crossref: 45] [Cited by in F6Publishing: 47] [Article Influence: 22.5] [Reference Citation Analysis]
27 Yin T, Yan Y, Yang X, Li W. Flavonoids from tribe Delphineae (Ranunculaceae): Phytochemical review and chemotaxonomic value. Biochemical Systematics and Ecology 2021;97:104300. [DOI: 10.1016/j.bse.2021.104300] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
28 Yu K, Yao F, Zeng Q, Xie H, Ding H. Asymmetric Total Syntheses of (+)-Davisinol and (+)-18-Benzoyldavisinol: A HAT-Initiated Transannular Redox Radical Approach. J Am Chem Soc 2021;143:10576-81. [PMID: 34240855 DOI: 10.1021/jacs.1c05703] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 3.5] [Reference Citation Analysis]
29 Xu JB, Li YZ, Huang S, Chen L, Luo YY, Gao F, Zhou XL. Diterpenoid alkaloids from the whole herb of Delphinium grandiflorum L. Phytochemistry 2021;190:112866. [PMID: 34271299 DOI: 10.1016/j.phytochem.2021.112866] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 3.5] [Reference Citation Analysis]
30 Thawabteh AM, Thawabteh A, Lelario F, Bufo SA, Scrano L. Classification, Toxicity and Bioactivity of Natural Diterpenoid Alkaloids. Molecules 2021;26:4103. [PMID: 34279443 DOI: 10.3390/molecules26134103] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 3.5] [Reference Citation Analysis]
31 Han J, Hou W, Cai BQ, Zhang F, Tang JC. 12-Epi-Napelline Inhibits Leukemia Cell Proliferation via the PI3K/AKT Signaling Pathway In Vitro and In Vivo. Evid Based Complement Alternat Med 2021;2021:6687519. [PMID: 34306152 DOI: 10.1155/2021/6687519] [Reference Citation Analysis]
32 Li Q, Wu B, Gong X, Wang W, Zhu J, Zhang C, Zhang N. Qualitative and quantitative analyses of aconite alkaloids in Aconiti kusnezoffii Radix, and NO inhibitory activity evaluation of the alkaloid extracts. Food Sci Technol. [DOI: 10.1590/fst.28521] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
33 Li H, Xu J, Zhang X, Liu C, Chen N, Naruo A, Qin Z, Ao M. New napelline-type diterpenoid alkaloids from Aconiti kusnezoffii roots: Structure elucidation, plausible biogenetic pathway and biological activities. Phytochemistry Letters 2021;43:53-9. [DOI: 10.1016/j.phytol.2021.03.007] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
34 Zhang Q, Yang Z, Wang Q, Liu S, Zhou T, Zhao Y, Zhang M. Asymmetric Total Synthesis of Hetidine-Type C20-Diterpenoid Alkaloids: (+)-Talassimidine and (+)-Talassamine. J Am Chem Soc 2021;143:7088-95. [PMID: 33938219 DOI: 10.1021/jacs.1c01865] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
35 Wang Y, Sun D, Chen Y, Xu J, Xu Y, Yue X, Jia J, Li H, Chen L. Alkaloids of Delphinium grandiflorum and their implication to H2O2-induced cardiomyocytes injury. Bioorganic & Medicinal Chemistry 2021;37:116113. [DOI: 10.1016/j.bmc.2021.116113] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
36 Zhang N, Xia F, Li SY, Nian Y, Wei LX, Xu G. Diterpenoid Alkaloids from the Aerial Parts of Aconitum flavum Hand.-Mazz. Nat Prod Bioprospect 2021;11:421-9. [PMID: 33861417 DOI: 10.1007/s13659-021-00302-3] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
37 Wu X, Nie W, Fu M, Liu X, Xue F, Qin Y. Synthetic studies towards arcutinidine: An alternative strategy for construction of the complete carbon framework. Tetrahedron 2021;86:132092. [DOI: 10.1016/j.tet.2021.132092] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
38 Shimakawa T, Hagiwara K, Inoue M. Total Synthesis of Talatisamine: Exploration of Convergent Synthetic Strategies. BCSJ 2021;94:973-983. [DOI: 10.1246/bcsj.20200400] [Reference Citation Analysis]
39 Wan LX, Zhang JF, Zhen YQ, Zhang L, Li X, Gao F, Zhou XL. Isolation, Structure Elucidation, Semi-Synthesis, and Structural Modification of C19-Diterpenoid Alkaloids from Aconitum apetalum and Their Neuroprotective Activities. J Nat Prod 2021;84:1067-77. [PMID: 33666437 DOI: 10.1021/acs.jnatprod.0c01111] [Cited by in Crossref: 13] [Cited by in F6Publishing: 14] [Article Influence: 6.5] [Reference Citation Analysis]
40 Gabbasov TM, Tsyrlina EM, Yunusov MS. Unexpected Products of the Reaction of Lappaconitine-Based Nitrone with N,N-Diethylallylamine. Dokl Chem 2020;495:175-7. [DOI: 10.1134/s0012500820110038] [Reference Citation Analysis]
41 Liu XY, Wang FP, Qin Y. Synthesis of Three-Dimensionally Fascinating Diterpenoid Alkaloids and Related Diterpenes. Acc Chem Res 2021;54:22-34. [PMID: 33351595 DOI: 10.1021/acs.accounts.0c00720] [Cited by in Crossref: 10] [Cited by in F6Publishing: 11] [Article Influence: 5.0] [Reference Citation Analysis]
42 Drummond GJ, Grant PS, Brimble MA. ent-Atisane diterpenoids: isolation, structure and bioactivity. Nat Prod Rep 2021;38:330-45. [PMID: 32716458 DOI: 10.1039/d0np00039f] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]
43 Zhou X, Chen L, Qin L, Xing F. A New Denudatine Type C20-Diterpenoid Alkaloid from Aconitum fischeri var. arcuatum. HETEROCYCLES 2021;102:1330. [DOI: 10.3987/com-21-14462] [Reference Citation Analysis]
44 Yu Y, Wu S, Zhang J, Li J, Yao C, Wu W, Wang Y, Ji H, Wei W, Gao M, Li Y, Yao S, Huang Y, Bi Q, Qu H, Guo D. Structurally diverse diterpenoid alkaloids from the lateral roots of Aconitum carmichaelii Debx. and their anti-tumor activities based on in vitro systematic evaluation and network pharmacology analysis. RSC Adv 2021;11:26594-26606. [DOI: 10.1039/d1ra04223h] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
45 Liu H, Wu Y, Guo Q, Shao S, Xu C, Zhang T, Shi J. Aconapelsulfonines A and B, seco C20-diterpenoid alkaloids deriving via Criegee rearrangements of napelline skeleton from Aconitum carmichaelii. Chinese Chemical Letters 2021;32:33-6. [DOI: 10.1016/j.cclet.2020.09.062] [Cited by in Crossref: 7] [Cited by in F6Publishing: 9] [Article Influence: 3.5] [Reference Citation Analysis]
46 Zhou X, Song Z, Xu K, Li J, Xie Y, Li X, Huang S, Gao F, Chen L. Semi-Synthetic Chasmanthinine Analogues with Antifeedant Effects against Spodoptera exigua. HETEROCYCLES 2021;102:2341. [DOI: 10.3987/com-21-14544] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
47 Ablajan N, Zhao B, Zhao JY, Wang BL, Sagdullaev SS, Aisa HA. Diterpenoid alkaloids from Aconitum barbatum var. puberulum Ledeb. Phytochemistry 2021;181:112567. [PMID: 33197742 DOI: 10.1016/j.phytochem.2020.112567] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
48 Chen LL, Lai CJ, Mao LY, Yin BW, Tian M, Jin BL, Wei XY, Chen JL, Ge H, Zhao X, Li WY, Guo J, Cui GH, Huang LQ. Chemical constituents in different parts of seven species of Aconitum based on UHPLC-Q-TOF/MS. J Pharm Biomed Anal 2021;193:113713. [PMID: 33160222 DOI: 10.1016/j.jpba.2020.113713] [Cited by in Crossref: 8] [Cited by in F6Publishing: 10] [Article Influence: 2.7] [Reference Citation Analysis]
49 Huang H, Mi F, Li C, He H, Wang F, Liu X, Qin Y. Total Synthesis of Liangshanone. Angew Chem 2020;132:23815-20. [DOI: 10.1002/ange.202011923] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
50 Huang H, Mi F, Li C, He H, Wang F, Liu X, Qin Y. Total Synthesis of Liangshanone. Angew Chem Int Ed 2020;59:23609-14. [DOI: 10.1002/anie.202011923] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 2.7] [Reference Citation Analysis]
51 Si Y, Ding X, Adelakuna TA, Zhang Y, Hao XJ. Acotarines A-G, new diterpenoid alkaloids from Aconitum taronense induce lysosomal biogenesis. Fitoterapia 2020;147:104738. [PMID: 33031866 DOI: 10.1016/j.fitote.2020.104738] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
52 Guo Q, Xia H, Wu Y, Shao S, Xu C, Zhang T, Shi J. Structure, property, biogenesis, and activity of diterpenoid alkaloids containing a sulfonic acid group from Aconitum carmichaelii. Acta Pharm Sin B 2020;10:1954-65. [PMID: 33163346 DOI: 10.1016/j.apsb.2020.01.013] [Cited by in Crossref: 11] [Cited by in F6Publishing: 14] [Article Influence: 3.7] [Reference Citation Analysis]
53 Huang S, Zhang J, Chen L, Gao F, Zhou X. Diterpenoid alkaloids from Aconitum anthoroideum that offer protection against MPP+–Induced apoptosis of SH–SY5Y cells and acetylcholinesterase inhibitory activity. Phytochemistry 2020;178:112459. [DOI: 10.1016/j.phytochem.2020.112459] [Cited by in Crossref: 12] [Cited by in F6Publishing: 9] [Article Influence: 4.0] [Reference Citation Analysis]
54 Shu Y, Wang J, Cai X, Li X, Hu J, Sun C, Cai L, Ding Z. Stylosines A and B, anti-inflammatory diterpenoid alkaloids from Aconitum stylosum. Tetrahedron 2020;76:131520. [DOI: 10.1016/j.tet.2020.131520] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 2.7] [Reference Citation Analysis]
55 Yin T, Cai L, Ding Z. A systematic review on the chemical constituents of the genus Consolida (Ranunculaceae) and their biological activities. RSC Adv 2020;10:35072-89. [PMID: 35515663 DOI: 10.1039/d0ra06811j] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
56 Chen S, Meng L, El-demerdash FM, Zhou L, Rizvi SAH, Cui L, Kang W. Review of Compounds and Pharmacological Effects of Delphinium. Journal of Chemistry 2020;2020:1-23. [DOI: 10.1155/2020/9375619] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
57 Schuppe AW, Liu Y, Newhouse TR. An invocation for computational evaluation of isomerization transforms: cationic skeletal reorganizations as a case study. Nat Prod Rep 2021;38:510-27. [PMID: 32931541 DOI: 10.1039/d0np00005a] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
58 Umekubo N, Hayashi Y. Asymmetric One‐Pot Mukaiyama Michael/Michael Reaction Catalyzed by Diphenylprolinol Silyl Ether. Eur J Org Chem 2020;2020:5596-600. [DOI: 10.1002/ejoc.202000925] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
59 Minagawa K, Kamakura D, Hagiwara K, Inoue M. Construction of the ABCE-ring structure of talatisamine via decarboxylative radical cyclization. Tetrahedron 2020;76:131385. [DOI: 10.1016/j.tet.2020.131385] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
60 Shen X, Yin T, Li X, Ma J, Lv Q, Zhang G. Diterpenoid alkaloids with chemotaxonomic significance from Aconitum spathulatum. Biochemical Systematics and Ecology 2020;91:104045. [DOI: 10.1016/j.bse.2020.104045] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
61 Zhao B, Ablajan N, Zhao J, Kodirova D, Sagdullaev S, Aisa H. Two new C19-diterpenoid alkaloids from Aconitum smirnovii. Phytochemistry Letters 2020;38:96-100. [DOI: 10.1016/j.phytol.2020.05.007] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
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64 Meng Z, Mi F, Lu F, Tan W, Liu X, Qin Y. Assembly of the 6/3/5/6 tetracyclic core of rearranged-type C19-diterpenoid alkaloids. Chinese Chemical Letters 2020;31:1903-1905. [DOI: 10.1016/j.cclet.2020.01.043] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
65 Li Y, Qin L, Gao F, Shan L, Zhou X. Kusnezosines A-C, three C19-diterpenoid alkaloids with a new skeleton from Aconitum kusnezoffii Reichb. var. gibbiferum. Fitoterapia 2020;144:104609. [DOI: 10.1016/j.fitote.2020.104609] [Cited by in Crossref: 10] [Cited by in F6Publishing: 6] [Article Influence: 3.3] [Reference Citation Analysis]
66 Heravi MM, Janati F, Zadsirjan V. Applications of Knoevenagel condensation reaction in the total synthesis of natural products. Monatsh Chem 2020;151:439-82. [DOI: 10.1007/s00706-020-02586-6] [Cited by in Crossref: 27] [Cited by in F6Publishing: 26] [Article Influence: 9.0] [Reference Citation Analysis]
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68 Doering NA, Sarpong R, Hoffmann RW. A Case for Bond-Network Analysis in the Synthesis of Bridged Polycyclic Complex Molecules: Hetidine and Hetisine Diterpenoid Alkaloids. Angew Chem Int Ed Engl 2020;59:10722-31. [PMID: 31808282 DOI: 10.1002/anie.201909656] [Cited by in Crossref: 12] [Cited by in F6Publishing: 15] [Article Influence: 4.0] [Reference Citation Analysis]
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