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

• 資料種別: 記事
• タイトル: Isolation, identification, and DFT-based conformational analysis of sesquikarahanadienone and its congeners from freshwater Dothideomycetes Neohelicascus aquaticus KT4120
• 著者・編者: Ayane Hayasaka; Kazuki Hashimoto; Katsuhiro Konno
• 出版事項: 日本 : The Chemical Society of Japan
• 出版年月日等: 2022-03-26
• 出版年（W3CDTF）: 2022-03-26
• タイトル（掲載誌）: Bulletin of the Chemical Society of Japan
• 巻号年月日等（掲載誌）: 95(5)
• 掲載巻: 95(5)
• ISSN（掲載誌）: 1348-0634
• ISSN-L（掲載誌）: 0009-2673
• 本文の言語コード: eng
• DOI: 10.1246/bcsj.20220063; https://doi.org/10.1246/bcsj.20220063
• 国立国会図書館永続的識別子: info:ndljp/pid/12686437; https://dl.ndl.go.jp/pid/12686437
• コレクション（共通）: 障害者向け資料
• コレクション（障害者向け資料：レベル1）: テキストデータ
• コレクション（個別）: 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
• 収集根拠: オンライン資料収集制度
• 受理日（W3CDTF）: 2023-03-07T17:43:09+09:00
• 保存日（W3CDTF）: 2023-01-20
• 記録形式（IMT）: application/pdf
• オンライン閲覧公開範囲: 国立国会図書館内限定公開
• デジタル化資料送信: 図書館・個人送信対象外
• 遠隔複写可否（NDL）: 可
• 掲載誌（URI）: https://www.journal.csj.jp/toc/bcsj/95/5
• 掲載誌（国立国会図書館永続的識別子）: info:ndljp/pid/12686433; https://dl.ndl.go.jp/pid/12686433
• 連携機関・データベース: 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

• 要約等: 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
• オンライン閲覧公開範囲: インターネット公開
• 関連情報（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
• 参照: 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
• 参照: Revision of the<i>Massarineae</i>(<i>Pleosporales</i>,<i>Dothideomycetes</i>); https://cir.nii.ac.jp/crid/1360002216159634048; Neomacrophorin I, II, and III, novel drimenyl cyclohexanes with hydroxylated butanoates from Trichoderma sp. 1212-03; https://cir.nii.ac.jp/crid/1360002216176604288; New Bioactive Metabolites from a Freshwater Isolate of the Fungus Kirschsteiniothelia sp.; https://cir.nii.ac.jp/crid/1360016868645463168; Trichoderma: A Treasure House of Structurally Diverse Secondary Metabolites With Medicinal Importance; https://cir.nii.ac.jp/crid/1360016870096242560; Isolation of Peribysins O, P, and Q from <i>Periconia macrospinosa</i> KT3863 and Configurational Reinvestigation of Peribysin E Diacetate from <i>Periconia byssoides</i> OUPS-N133; https://cir.nii.ac.jp/crid/1360285708106927872; Decaspirones and palmarumycins from Phaeoseptum sp. KT4106: Chirality reinvestigation of palmarumycins CP4a and CP5; https://cir.nii.ac.jp/crid/1360294643780698496; Computational NMR Methods in the Stereochemical Analysis of Organic Compounds: Are Proton or Carbon NMR Chemical Shift Data More Discriminating?; https://cir.nii.ac.jp/crid/1360298341957468672; Cyclohumulanoid Sesquiterpenes from the Culture Broth of the Basidiomycetous Fungus Daedaleopsis tricolor; https://cir.nii.ac.jp/crid/1360298342474716416; Trichocarotins A–H and trichocadinin A, nine sesquiterpenes from the marine-alga-epiphytic fungus Trichoderma virens; https://cir.nii.ac.jp/crid/1360298345303784960; Metabolites of Pyrenomycetes: XII. Polyketides from the Hypocreales; https://cir.nii.ac.jp/crid/1360298345359094912; Structure of sesquicarene; https://cir.nii.ac.jp/crid/1360298345509826816; Recommended names for pleomorphic genera in Dothideomycetes; https://cir.nii.ac.jp/crid/1360565171131801088; 7-β- and 10-β-Hydroxylated congeners of CAF-603; elucidation of absolute configuration of CAF-603 family, and their SAR studies in the anti-fungal activity; https://cir.nii.ac.jp/crid/1360567182478505600; Freshwater Dothideomycetes; https://cir.nii.ac.jp/crid/1360572092640968576; Density-functional thermochemistry. III. 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. KTC 727; https://cir.nii.ac.jp/crid/1361137046105427584; Isolation, structure, and synthesis of chenopodanol and the absolute configuration of chenopodene and chenopodanol; https://cir.nii.ac.jp/crid/1361418521072363520; Evaluation of culture media for the production of secondary metabolites in a natural products screening program; https://cir.nii.ac.jp/crid/1361699995670709248; Development of a ¹³C NMR Chemical Shift Prediction Procedure Using B3LYP/cc-pVDZ and Empirically Derived Systematic Error Correction Terms: A Computational Small Molecule Structure Elucidation Method; https://cir.nii.ac.jp/crid/1361981469023820032; NMR Calculations with Quantum Methods: Development of New Tools for Structural Elucidation and Beyond; https://cir.nii.ac.jp/crid/1362262944004439808; Regiolone and Isosclerone, Two Enantiomeric Phytotoxic Naphthalenone Pentaketides: Computational Assignment of Absolute Configuration and Its Relationship with Phytotoxic Activity; https://cir.nii.ac.jp/crid/1362262944694796544; The Conservation of Orbital Symmetry; https://cir.nii.ac.jp/crid/1362544419369297152; Oxidation of long-chain and related alcohols to carbonyls by dimethyl sulfoxide "activated" by oxalyl chloride; https://cir.nii.ac.jp/crid/1363107369018452736; Efficient Protocol for Accurately Calculating ¹³C Chemical Shifts of Conformationally Flexible Natural Products: Scope, Assessment, and Limitations; https://cir.nii.ac.jp/crid/1363388844346574464; Molecular genetic analysis of the orsellinic acid/F9775 genecluster of <i>Aspergillus nidulans</i>; https://cir.nii.ac.jp/crid/1363388845153348224; Carbon-13 magnetic resonance. XXI. Steric interactions in the methylcyclohexanes; https://cir.nii.ac.jp/crid/1363670319542148736; (−)-Regiolone, an α-tetralone from Juglans regia: structure, stereochemistry and conformation; https://cir.nii.ac.jp/crid/1363670319591411072; ωB97X-V: A 10-parameter, range-separated hybrid, generalized gradient approximation density functional with nonlocal correlation, designed by a survival-of-the-fittest strategy; https://cir.nii.ac.jp/crid/1363951794056713600; The M06 suite of density functionals for main group thermochemistry, thermochemical kinetics, noncovalent interactions, excited states, and transition elements: two new functionals and systematic testing of four M06-class functionals and 12 other functionals; https://cir.nii.ac.jp/crid/1363951794362548224; A Series of Well‐Defined Metathesis Catalysts–Synthesis of [RuCl₂(CHR′)(PR₃)₂] and Its Reactions; https://cir.nii.ac.jp/crid/1364233270473080448; A new hybrid exchange–correlation functional using the Coulomb-attenuating method (CAM-B3LYP); https://cir.nii.ac.jp/crid/1364233271143226624; Phenyl Ethers from Cultured Lichen Mycobionts of Graphis scripta var. serpentina and G. rikuzensis; https://cir.nii.ac.jp/crid/1390001204165404032; Isolation and Absolute Stereochemistry of Optically Active Sydonic Acid from<i>Glonium</i>sp. (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
• 参照（URI）: https://cir.nii.ac.jp/crid/1370009584234368697; https://cir.nii.ac.jp/crid/1370298337057490567; https://cir.nii.ac.jp/crid/1370298337057490569
• 連携機関・データベース: 国立情報学研究所 : CiNii Research; https://cir.nii.ac.jp/
• 提供元機関・データベース: 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
• 書誌ID（NDLBibID）: 12686437; http://id.ndl.go.jp/bib/12686437