Isolation, identification, and DFT-based conformational analysis of sesquikarahanadienone and its congeners from freshwater Dothideomycetes Neohelicascus aquaticus KT4120

• Material Type: 記事
• Title: Isolation, identification, and DFT-based conformational analysis of sesquikarahanadienone and its congeners from freshwater Dothideomycetes Neohelicascus aquaticus KT4120
• Author/Editor: Ayane Hayasaka; Kazuki Hashimoto; Katsuhiro Konno
• Publication, Distribution, etc.: 日本 : The Chemical Society of Japan
• Publication Date: 2022-03-26
• Publication Date (W3CDTF): 2022-03-26
• Periodical title: Bulletin of the Chemical Society of Japan
• No. or year of volume/issue: 95(5)
• Volume: 95(5)
• ISSN (Periodical Title): 1348-0634
• ISSN-L (Periodical Title): 0009-2673
• Text Language Code: eng
• DOI: 10.1246/bcsj.20220063; https://doi.org/10.1246/bcsj.20220063
• Persistent ID (NDL): info:ndljp/pid/12686437; https://dl.ndl.go.jp/pid/12686437
• Collection: 障害者向け資料
• Collection (Materials For Handicapped People:1): テキストデータ
• Collection (particular): 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > 学術機関 > 学協会; https://dl.ndl.go.jp/collections/B00043
• Acquisition Basis: オンライン資料収集制度
• Date Accepted (W3CDTF): 2023-03-07T17:43:09+09:00
• Date Captured (W3CDTF): 2023-01-20
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• Periodical Title (URI): https://www.journal.csj.jp/toc/bcsj/95/5
• Periodical Title (Persistent ID (NDL)): info:ndljp/pid/12686433; https://dl.ndl.go.jp/pid/12686433
• Data Provider (Database): 国立国会図書館 : 国立国会図書館デジタルコレクション; https://dl.ndl.go.jp

• Summary, etc.: コレクション : 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > 学術機関 > 学協会
• DOI: 10.1246/bcsj.20220063; https://doi.org/10.1246/bcsj.20220063
• Access Restrictions: インターネット公開
• Related Material (URI): http://id.ndl.go.jp/digimeta/12686437; https://dl.ndl.go.jp/pid/12686437; https://academic.oup.com/bcsj/article-pdf/95/5/833/56317831/bcsj.20220063.pdf
• Is Referenced By: Structural Determination, Total Synthesis, and Biological Activity of Iezoside, a Highly Potent Ca²⁺-ATPase Inhibitor from the Marine Cyanobacterium <i>Leptochromothrix valpauliae</i>; https://cir.nii.ac.jp/crid/1360017282207954304; Kagimminols A and B, Cembrene-Type Diterpenes from an <i>Okeania</i> sp. Marine Cyanobacterium; https://cir.nii.ac.jp/crid/1360021391860374784; Pseudo-Enantiomeric Paraphaeolactones and Their Biosynthetic Derivatives from <i>Paraphaeosphaeria</i> sp. KT4192: A Proposition of a Favorskii Rearrangement for Their Biosynthesis; https://cir.nii.ac.jp/crid/1360021391872191744; Highly Functionalized Spirobisnaphthalenes from <i>Roussoella</i> sp. KT4147; https://cir.nii.ac.jp/crid/1360025429412107392; Integrasone Derivatives Isolated from <i>Lepteutypa</i> sp. KT4162 and Their Anti-HIV-1 Integrase Activity; https://cir.nii.ac.jp/crid/1360580232412834560; Gregarithecinol, a trichodiene/bazzanene derivative from Gregarithecium curvisporum KT4079: DFT-supported stereochemical elucidation of units linked by a rotatable bond; https://cir.nii.ac.jp/crid/1360588380131430400; Stereoselective Preparation of the Tricyclic Hexasubstituted Spirocyclopropane Core of Cyclohelminthol X; https://cir.nii.ac.jp/crid/1360864735223487744; Triantaspirols A–C and Paraphaeolactone Cs from <i>Paraphaeosphaeria</i> sp. KT4192: Sensitivity of CP3 in Distinguishing Close NMR Signals; https://cir.nii.ac.jp/crid/1360869854343108096
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The role of exact exchange; https://cir.nii.ac.jp/crid/1360574092888916224; A consistent and accurate<i>ab initio</i>parametrization of density functional dispersion correction (DFT-D) for the 94 elements H-Pu; https://cir.nii.ac.jp/crid/1360574095458564352; The biosynthesis of phenols—XVII; https://cir.nii.ac.jp/crid/1360574095652511744; Ymf 1029A−E, Preussomerin Analogues from the Fresh-Water-Derived Fungus YMF 1.01029; https://cir.nii.ac.jp/crid/1360579819034892928; DFT Supported Structural Revision of Seiricardines; https://cir.nii.ac.jp/crid/1360848661918496768; Cyclohelminthol CPs: Scope and Limitations of Density Functional Theory-Based Structural Elucidation of Natural Products; https://cir.nii.ac.jp/crid/1360853567616201344; Optimization of the Microwave-Assisted Ortho Ester Claisen Rearrangement: Application to Monoterpenols; https://cir.nii.ac.jp/crid/1360855568652877056; Isoepoxydon, a new metabolite of the patulin pathway in <i>Penicillium urticae</i>; https://cir.nii.ac.jp/crid/1360855569448099328; A new mixing of Hartree–Fock and local density-functional theories; https://cir.nii.ac.jp/crid/1360855570536878080; The Risks of Automation: A Study on DFT Energy Miscalculations and Its Consequences in NMR-based Structural Elucidation; https://cir.nii.ac.jp/crid/1360855571007658240; New monoterpenoids from hop oil; https://cir.nii.ac.jp/crid/1360861291359765376; Freshwater Fungi as a Source of Chemical Diversity: A Review; https://cir.nii.ac.jp/crid/1360861294710730112; Prenylated Diresorcinols Inhibit Bacterial Quorum Sensing; https://cir.nii.ac.jp/crid/1360861295234750336; Assigning Stereochemistry to Single Diastereoisomers by GIAO NMR Calculation: The DP4 Probability; https://cir.nii.ac.jp/crid/1361137043564015744; The Basis Set Convergence of Spin−Spin Coupling Constants Calculated by Density Functional Methods; https://cir.nii.ac.jp/crid/1361137044549832960; Long-range corrected hybrid density functionals with damped atom–atom dispersion corrections; https://cir.nii.ac.jp/crid/1361137044564975360; Stereochemical Investigations of Isochromenones and Isobenzofuranones Isolated from <i>Leptosphaeria</i> sp. 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(Hysteriales, Ascomycota); https://cir.nii.ac.jp/crid/1390001206480217600; ChemInform Abstract: A New Azaphilone, Falconensin H, from Emericella falconensis.; https://cir.nii.ac.jp/crid/1390282679135635840
• References (URI): https://cir.nii.ac.jp/crid/1370009584234368697; https://cir.nii.ac.jp/crid/1370298337057490567; https://cir.nii.ac.jp/crid/1370298337057490569
• Data Provider (Database): 国立情報学研究所 : CiNii Research; https://cir.nii.ac.jp/
• Original Data Provider (Database): 雑誌記事索引データベース; https://ndlsearch.ndl.go.jp; Crossref; https://www.crossref.org; 科学研究費助成事業データベース; https://kaken.nii.ac.jp/ja
• Bibliographic ID (NDL): 12686437; http://id.ndl.go.jp/bib/12686437