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Synthetic Transformations of Higher Terpenoids. 45<sup>#</sup>. Regioselective Synthesis of 5-Labdanoid-Substituted Pyrazoles and Assessment of Their Analgesic Activity.
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- Chemistry of Natural Compounds, 2024, v. 60, n. 4, p. 662, doi. 10.1007/s10600-024-04408-1
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- Article
Activity difference of three labdane diterpenoids on human constitutive androstane receptor.
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- Bioscience, Biotechnology & Biochemistry, 2023, v. 87, n. 11, p. 1310, doi. 10.1093/bbb/zbad113
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Insight into the mechanism of geranyl-β-phellandrene formation catalyzed by Class IB terpene synthases.
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- Bioscience, Biotechnology & Biochemistry, 2022, v. 86, n. 6, p. 724, doi. 10.1093/bbb/zbac036
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Functional kaurene-synthase-like diterpene synthases lacking a gamma domain are widely present in Oryza and related species.
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- Bioscience, Biotechnology & Biochemistry, 2021, v. 85, n. 9, p. 1945, doi. 10.1093/bbb/zbab127
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Recent advances in the total syntheses of indole diterpenoids.
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- Bioscience, Biotechnology & Biochemistry, 2021, v. 85, n. 1, p. 13, doi. 10.1093/bbb/zbaa061
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Biosynthetic study of conidiation-inducing factor conidiogenone: heterologous production and cyclization mechanism of a key bifunctional diterpene synthase.
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- Bioscience, Biotechnology & Biochemistry, 2019, v. 83, n. 2, p. 192, doi. 10.1080/09168451.2018.1536518
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Inhibitory effect of 13 taxane diterpenoids from Chinese yew ( Taxus chinensis var. mairei ) on the proliferation of HeLa cervical cancer cells.
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- Bioscience, Biotechnology & Biochemistry, 2016, v. 80, n. 10, p. 1883, doi. 10.1080/09168451.2016.1194182
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Inhibition of human neutrophil elastase by labdane diterpenes from the fruiting bodies of <italic>Ramaria formosa</italic>.
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- Bioscience, Biotechnology & Biochemistry, 2015, v. 79, n. 12, p. 1921, doi. 10.1080/09168451.2015.1065168
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Asymmetric Total Syntheses of Di‐ and Sesquiterpenoids by Catalytic C−C Activation of Cyclopentanones.
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- Angewandte Chemie, 2020, v. 132, n. 20, p. 7922, doi. 10.1002/ange.201915821
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- Article
Eine unerwartete transanulare [4+2]‐Cycloaddition während der Gesamtsynthese von (+)‐Norcembren 5.
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- Angewandte Chemie, 2020, v. 132, n. 14, p. 5564, doi. 10.1002/ange.201912613
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Total Synthesis and Structural Revision of a Harziane Diterpenoid.
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- Angewandte Chemie, 2020, v. 132, n. 3, p. 1208, doi. 10.1002/ange.201912982
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- Article
6‐Methylenebicyclo[3.2.1]oct‐1‐en‐3‐one: A Twisted Olefin as Diels–Alder Dienophile for Expedited Syntheses of Four Kaurane Diterpenoids.
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- Angewandte Chemie, 2019, v. 131, n. 44, p. 15878, doi. 10.1002/ange.201909349
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- Article
Total Syntheses of Rhodomolleins XX and XXII: A Reductive Epoxide‐Opening/Beckwith–Dowd Approach.
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- Angewandte Chemie, 2019, v. 131, n. 25, p. 8644, doi. 10.1002/ange.201903349
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Synthesis of (+)‐Darwinolide, a Biofilm‐Penetrating Anti‐MRSA Agent.
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- Angewandte Chemie, 2019, v. 131, n. 4, p. 1132, doi. 10.1002/ange.201813142
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- Article
Enantioselective Total Synthesis of (+)‐Plumisclerin A.
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- Angewandte Chemie, 2018, v. 130, n. 40, p. 13497, doi. 10.1002/ange.201808517
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A Unified Approach for the Assembly of Atisine‐ and Hetidine‐type Diterpenoid Alkaloids: Total Syntheses of Azitine and the Proposed Structure of Navirine C.
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- Angewandte Chemie, 2018, v. 130, n. 22, p. 6786, doi. 10.1002/ange.201803018
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A Kinetic Dearomatization Strategy for an Expedient Biomimetic Route to the Bielschowskysin Skeleton.
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- Angewandte Chemie, 2018, v. 130, n. 5, p. 1330, doi. 10.1002/ange.201711780
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Divergent Asymmetric Total Synthesis of Mulinane Diterpenoids.
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- Angewandte Chemie, 2017, v. 129, n. 41, p. 12882, doi. 10.1002/ange.201706994
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A Concise Synthesis of Forskolin.
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- Angewandte Chemie, 2017, v. 129, n. 41, p. 12760, doi. 10.1002/ange.201706809
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Total Syntheses of the Reported Structures of Curcusones I and J through Tandem Gold Catalysis.
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- Angewandte Chemie, 2017, v. 129, n. 38, p. 11782, doi. 10.1002/ange.201706845
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Total Synthesis of (±)-Waihoensene.
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- Angewandte Chemie, 2017, v. 129, n. 28, p. 8366, doi. 10.1002/ange.201704492
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Discovery and Characterization of a New Family of Diterpene Cyclases in Bacteria and Fungi.
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- Angewandte Chemie, 2017, v. 129, n. 17, p. 4827, doi. 10.1002/ange.201700565
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Total Synthesis of the Diterpenoid (+)-Harringtonolide.
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- Angewandte Chemie, 2016, v. 128, n. 38, p. 11810, doi. 10.1002/ange.201605879
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Total Syntheses of the Tetracyclic Cyclopiane Diterpenes Conidiogenone, Conidiogenol, and Conidiogenone B.
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- Angewandte Chemie, 2016, v. 128, n. 14, p. 4532, doi. 10.1002/ange.201600529
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Total Synthesis of Ileabethoxazole, Pseudopteroxazole, and seco-Pseudopteroxazole.
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- Angewandte Chemie, 2016, v. 128, n. 8, p. 2901, doi. 10.1002/ange.201510568
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- Article
Collective Total Syntheses of Atisane-Type Diterpenes and Atisine-Type Diterpenoid Alkaloids: (±)-Spiramilactone B, (±)-Spiraminol, (±)-Dihydroajaconine, and (±)-Spiramines C and D.
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- Angewandte Chemie, 2016, v. 128, n. 1, p. 400, doi. 10.1002/ange.201508996
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Total Synthesis of Crotophorbolone.
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- Angewandte Chemie, 2015, v. 127, n. 48, p. 14665, doi. 10.1002/ange.201509160
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Protecting-Group-Free Enantioselective Synthesis of (−)-Pallavicinin and (+)-Neopallavicinin.
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- Angewandte Chemie, 2015, v. 127, n. 46, p. 13803, doi. 10.1002/ange.201506575
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Total Synthesis of Diterpenoid Steenkrotin A.
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- Angewandte Chemie, 2015, v. 127, n. 23, p. 7009, doi. 10.1002/ange.201502034
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Reconstitution of Biosynthetic Machinery for the Synthesis of the Highly Elaborated Indole Diterpene Penitrem.
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- Angewandte Chemie, 2015, v. 127, n. 19, p. 5840, doi. 10.1002/anie.201501072
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Enantioselective Palladium-Catalyzed Dearomative Cyclization for the Efficient Synthesis of Terpenes and Steroids.
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- Angewandte Chemie, 2015, v. 127, n. 10, p. 3076, doi. 10.1002/ange.201411817
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Conceptualization of a spent coffee grounds biorefinery: A review of existing valorisation approaches.
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- Food & Bioproducts Processing: Transactions of the Institution of Chemical Engineers Part C, 2019, v. 118, n. Part C, p. 149, doi. 10.1016/j.fbp.2019.08.010
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Structure-activity relationship studies of the phytotoxic properties of the diterpenic moiety of breviones.
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- Pest Management Science, 2015, v. 71, n. 5, p. 701, doi. 10.1002/ps.3831
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Molluscicidal and anti-feedant activities of diterpenes from Euphorbia paralias L.
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- Pest Management Science, 2002, v. 58, n. 5, p. 479, doi. 10.1002/ps.487
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Application of Terpenoid Compounds in Food and Pharmaceutical Products.
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- Fermentation (Basel), 2023, v. 9, n. 2, p. 119, doi. 10.3390/fermentation9020119
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Enhanced Production and in situ Product Recovery of Fusicocca-2,10(14)-Diene from Yeast.
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- Fermentation (Basel), 2018, v. 4, n. 3, p. 1, doi. 10.3390/fermentation4030065
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大型担子菌中二萜化合物生物合成研究进展.
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- Mycosystema, 2023, v. 42, n. 1, p. 101, doi. 10.13346/j.mycosystema.220374
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大型真菌来源鸟巢烷型二萜研究进展.
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- Acta Edulis Fungi, 2021, v. 28, n. 2, p. 140, doi. 10.16488/i.cnki.1005-9873.2021.02.018
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Terpenoids as chemosystematic markers in selected fossil and extant species of pine ( Pinus, Pinaceae).
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- Botanical Journal of the Linnean Society, 2007, v. 154, n. 1, p. 129, doi. 10.1111/j.1095-8339.2007.00638.x
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A general survey and some taxonomic implications of diterpenes in the Asteraceae.
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- Botanical Journal of the Linnean Society, 2005, v. 147, n. 3, p. 291, doi. 10.1111/j.1095-8339.2005.00357.x
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Papillon-Lefèvre syndrome-Successful treatment with a combination of retinoid and concurrent systematic periodontal therapy: Case reports.
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- Quintessence International, 1995, v. 26, n. 11, p. 795
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大瑶山甜茶正丁醇部位化学成分研究.
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- Progress in Modern Biomedicine, 2019, v. 19, n. 3, p. 434, doi. 10.13241/j.cnki.pmb.2019.03.008
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- Article
Inferring Roles in Defense from Metabolic Allocation of Rice Diterpenoids.
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- Plant Cell, 2018, v. 30, n. 5, p. 1119, doi. 10.1105/tpc.18.00205
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Formation of the Unusual Semivolatile Diterpene Rhizathalene by the Arabidopsis Class I Terpene Synthase TPS08 in the Root Stele Is Involved in Defense against Belowground Herbivory.
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- Plant Cell, 2013, v. 25, n. 3, p. 1108, doi. 10.1105/tpc.112.100057
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Jasmonate and ppHsystemin Regulate Key Malonylation Steps in the Biosynthesis of 17-Hydroxygeranyllinalool Diterpene Glycosides, an Abundant and Effective Direct Defense against Herbivores in Nicotiana attenuata.
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- Plant Cell, 2010, v. 22, n. 1, p. 273, doi. 10.1105/tpc.109.071449
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Metal derivatives of diterpenoid isosteviol.
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- Russian Journal of General Chemistry, 2014, v. 84, n. 4, p. 700, doi. 10.1134/S1070363214040161
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Hybrid compounds of ent-beyerane diterpenoid isosteviol with pyridinecarboxylic acid hydrazides. Synthesis, structure, and antitubercular activity.
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- Russian Journal of General Chemistry, 2011, v. 81, n. 8, p. 1643, doi. 10.1134/S1070363211080111
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13-halo derivatives of ent-kauranoic acid. Synthesis and structure.
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- Russian Journal of General Chemistry, 2011, v. 81, n. 5, p. 927, doi. 10.1134/S1070363211050148
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O-Alkylation of diterpenoid steviol in the system KOH-DMSO.
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- Russian Journal of General Chemistry, 2009, v. 79, n. 10, p. 2197, doi. 10.1134/S1070363209100193
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New synthesis of diterpenoid (16 S)-dihydrosteviol.
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- Russian Journal of General Chemistry, 2009, v. 79, n. 5, p. 967, doi. 10.1134/S107036320905017X
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- Article