{"@context":{"@vocab":"https://cir.nii.ac.jp/schema/1.0/","rdfs":"http://www.w3.org/2000/01/rdf-schema#","dc":"http://purl.org/dc/elements/1.1/","dcterms":"http://purl.org/dc/terms/","foaf":"http://xmlns.com/foaf/0.1/","prism":"http://prismstandard.org/namespaces/basic/2.0/","cinii":"http://ci.nii.ac.jp/ns/1.0/","datacite":"https://schema.datacite.org/meta/kernel-4/","ndl":"http://ndl.go.jp/dcndl/terms/","jpcoar":"https://github.com/JPCOAR/schema/blob/master/2.0/"},"@id":"https://cir.nii.ac.jp/crid/1360565164376961024.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1002/anie.201104447"}},{"identifier":{"@type":"URI","@value":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fanie.201104447"}},{"identifier":{"@type":"URI","@value":"https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.201104447"}},{"identifier":{"@type":"DOI","@value":"10.1002/ange.201104447"}},{"identifier":{"@type":"URI","@value":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fange.201104447"}},{"identifier":{"@type":"URI","@value":"https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.201104447"}},{"identifier":{"@type":"PMID","@value":"21915975"}}],"resourceType":"学術雑誌論文(journal article)","dc:title":[{"@value":"Convergent Total Synthesis of (+)‐Ophiobolin A"}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1380566392498045440","@type":"Researcher","foaf:name":[{"@value":"Kazuhiro Tsuna"}]},{"@id":"https://cir.nii.ac.jp/crid/1380566392498045442","@type":"Researcher","foaf:name":[{"@value":"Naoyoshi Noguchi"}]},{"@id":"https://cir.nii.ac.jp/crid/1380566392498045441","@type":"Researcher","foaf:name":[{"@value":"Masahisa Nakada"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"14337851"},{"@type":"EISSN","@value":"15213773"},{"@type":"PISSN","@value":"00448249"},{"@type":"EISSN","@value":"15213757"}],"prism:publicationName":[{"@value":"Angewandte Chemie International Edition"}],"dc:publisher":[{"@value":"Wiley"}],"prism:publicationDate":"2011-09-13","prism:volume":"50","prism:number":"40","prism:startingPage":"9452","prism:endingPage":"9455"},"reviewed":"false","dc:rights":["http://onlinelibrary.wiley.com/termsAndConditions#vor"],"url":[{"@id":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fanie.201104447"},{"@id":"https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.201104447"},{"@id":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fange.201104447"},{"@id":"https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.201104447"}],"createdAt":"2011-09-13","modifiedAt":"2023-10-17","foaf:topic":[{"@id":"https://cir.nii.ac.jp/all?q=Sesterterpenes","dc:title":"Sesterterpenes"},{"@id":"https://cir.nii.ac.jp/all?q=Molecular%20Structure","dc:title":"Molecular Structure"},{"@id":"https://cir.nii.ac.jp/all?q=Stereoisomerism","dc:title":"Stereoisomerism"},{"@id":"https://cir.nii.ac.jp/all?q=Chemistry%20Techniques,%20Synthetic","dc:title":"Chemistry Techniques, Synthetic"}],"project":[{"@id":"https://cir.nii.ac.jp/crid/1040000782062530432","@type":"Project","projectIdentifier":[{"@type":"KAKEN","@value":"21106009"},{"@type":"JGN","@value":"JP21106009"},{"@type":"URI","@value":"https://kaken.nii.ac.jp/grant/KAKENHI-PLANNED-21106009/"}],"notation":[{"@language":"ja","@value":"立体選択的タンデム反応の開発と生物活性物質の集積合成への活用"},{"@language":"en","@value":"Synthetic Studies on Bioactive Natural Products utilizing Integrated"}]}],"relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1360002214465903360","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Enantioselective Total Synthesis of (+)‐Ophiobolin A"}]},{"@id":"https://cir.nii.ac.jp/crid/1360004232525963392","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Research on the pig liver esterase (PLE)-catalyzed kinetic resolution of half-esters derived from prochiral diesters"}]},{"@id":"https://cir.nii.ac.jp/crid/1360011143693812864","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Trisubstituted Double Bond in the Cyclooctene Ring. Preparation Using the RCM Reaction"}]},{"@id":"https://cir.nii.ac.jp/crid/1360011143727851136","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Total synthesis of albolic acid and ceroplastol II, 5–8–5-membered tricyclic insect sesterterpenoids, via a lactol-regulated silyloxy–Cope rearrangement"}]},{"@id":"https://cir.nii.ac.jp/crid/1360011145798011520","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Studies Towards the Total Synthesis of Di- and Sesterterpenes with Dicyclopenta[a,d]cyclooctane Skeletons. Three-component Approach to the A/B Rings Building Block"}]},{"@id":"https://cir.nii.ac.jp/crid/1360016866138590336","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Ring‐Closing Metathesis in the Synthesis of BC Ring‐Systems of Taxol"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285707501712384","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Syntheses of 6-8-5 tricyclic ring systems by carbonylative [2+2+1] cycloaddition of bis(allene)s"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285708157120384","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Convergent Strategies in Total Syntheses of Complex Terpenoids"}]},{"@id":"https://cir.nii.ac.jp/crid/1360292618680780416","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Selektiver Aufbau achtgliedriger Carbocyclen durch Ringschlussmetathese acyclischer Vorstufen"}]},{"@id":"https://cir.nii.ac.jp/crid/1360292620684070912","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthetic photochemistry. Part 44. Total synthesis of ceroplastol II and albolic acid, 5-8-5-membered tricyclic sesterterpenoid insect wax constituents, via stereocontrolled silyloxy-Cope rearrangement with a normally disfavoured transition state"}]},{"@id":"https://cir.nii.ac.jp/crid/1360292621185227392","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Ophiobolin M and analogues, noncompetitive inhibitors of ivermectin binding with nematocidal activity"}]},{"@id":"https://cir.nii.ac.jp/crid/1360565169056311424","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Studies on 5-8 Fused Ring Compounds. IV. The Syntheses of 5-8-5 Fused Ring Compounds and the Conformations of Their Eight-Membered Rings"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567182481386880","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Enantioselective preparation of C-ring fragment of cotylenin A via catalytic asymmetric intramolecular cyclopropanation of α-diazo β-keto ester"}]},{"@id":"https://cir.nii.ac.jp/crid/1360568468044032512","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Enantioselective Total Synthesis of Cotylenin A"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574093711090944","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"The biology of ophiobolins"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574094582557568","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthesis of the First \"Inside-Outside\" Eight-Membered Ring via Ring-Closing Metathesis: A Total Synthesis of (±)-Asteriscanolide"}]},{"@id":"https://cir.nii.ac.jp/crid/1360576118674868096","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis of the eight-membered carbocycle of brachialactone by intramolecular Mizoroki-Heck reaction"}]},{"@id":"https://cir.nii.ac.jp/crid/1360846641612341376","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis of the PMB Ether of 5,6-Epoxyisoprostane E2 through Aldol Reaction of the α-Bromocyclopentanone"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855568538690176","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Expedient Construction of the Dicyclopenta[<i>a</i>,<i>d</i>]cyclooctene Core of Ceroplastin Di- and Sesterterpenes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855568838056192","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Thermal reactions of alkyl N-carbomethoxysulfamate esters"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855569205486592","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"An oxyanionic [3,3]-sigmatropic approach to the ophiobolin ring system"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855570178425600","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A 4‐<i>exo</i>‐dig Cyclocarbopalladation/8π Electrocyclization Cascade: Expeditious Access to the Tricyclic Core Structures of the Ophiobolins and Aleurodiscal"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855570215164672","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A 4‐<i>exo</i>‐dig Cyclocarbopalladation/8π Electrocyclization Cascade: Expeditious Access to the Tricyclic Core Structures of the Ophiobolins and Aleurodiscal"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855570715599616","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthetic Studies on (+)-Ophiobolin A:  Asymmetric Synthesis of the Spirocyclic CD-Ring Moiety"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855570832380160","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"RCM for the Construction of Novel Steroid-like Polycyclic Systems. 1. Studies on the Synthesis of a PreD<sub>3</sub>-D<sub>3</sub>Transition State Analogue"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855570855163648","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"First Synthesis of a Rearranged <i>neo</i>-Clerodane Diterpenoid. Development of Totally Regioselective Trisubstituted Furan Ring Assembly and Medium-Ring Alkylation Tactics for Efficient Access to (−)-Teubrevin G"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855570929703296","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Phytotoxins from the pathogenic fungi\n            <i>Drechslera maydis</i>\n            and\n            <i>Drechslera sorghicola</i>"}]},{"@id":"https://cir.nii.ac.jp/crid/1360862100618588416","@type":"Article","relationType":["references"]},{"@id":"https://cir.nii.ac.jp/crid/1361137044083401344","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"The Development of L<sub>2</sub>X<sub>2</sub>RuCHR Olefin Metathesis Catalysts:  An Organometallic Success Story"}]},{"@id":"https://cir.nii.ac.jp/crid/1361137044184524288","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Selective Construction of Carbocyclic Eight‐Membered Rings by Ring‐Closing Metathesis of Acyclic Precursors"}]},{"@id":"https://cir.nii.ac.jp/crid/1361137046192329856","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Sesterterpenes. 1. Stereospecific construction of the ceroplastol and ophiobolin ring systems via a common bicyclic intermediate"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418518781609984","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthetic studies directed toward naturally occurring cyclooctanoids. 1. A total synthesis of (.+-.)-ceroplastol I."}]},{"@id":"https://cir.nii.ac.jp/crid/1361418520491696896","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthetic studies on the ophiobolane sesterterpenes: construction of an optically pure, advanced tricyclic intermediate for the synthesis of ceroplasteric acid"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699993538446208","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Enantioselective Double Michael Addition/Cyclization with an Oxygen-Centered Nucleophile as the First Step in a Concise Synthesis of Natural (+)-Asteriscanolide"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699994378571520","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"From Galactose to Highly Functionalized Seven- and Eight-Membered Carbocyclic Rings by Ring-Closing Metathesis"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699994625171584","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthesis of stereoisomeric 9a-methylhydrodicyclopenta[a,d]cyclooctan-1-ones related to the ophiobolins and ceroplastins via annelative ring expansion of hydrindene precursors"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981469718506240","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Total synthesis of (+)-ophiobolin C"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981469902929280","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A Very Rapid Stereocontrolled Entry to Highly Functionalized [5-8-5] Ring Systems Using the Saegusa Reaction"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981470508446976","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Access to naturally occurring cyclooctanoids by two-carbon intercalation. Total synthesis of (+)-ceroplastol I"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262943421865472","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Characterization of 6-<i>epi</i>-3-Anhydroophiobolin B from <i>Cochliobolus heterostrophus</i>"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262945599107328","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Facile routes to boron enolates. Et3B-mediated Reformatsky type reaction and three components coupling reaction of alkyl iodides, methyl vinyl ketone, and carbonyl compounds"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262945726917760","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthesis of Highly Functionalized Cyclooctenes by Ring-Closing Metathesis: Unexpected Formation of atrans Isomer"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262945983105280","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A synthesis of the ophiobolin nucleus"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262946060471552","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthetic applications of N-carboalkoxysulfamate esters"}]},{"@id":"https://cir.nii.ac.jp/crid/1362544418288260992","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Selected Substituent Effects on the Rate and Efficiency of Formation of an Eight-Membered Ring by RCM"}]},{"@id":"https://cir.nii.ac.jp/crid/1362544418542571392","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthetic studies on terpenoids. Part 19. Synthesis of 3β,10α,14β-trimethyl-1βH,11βH-tricyclo[9.3.0.0]tetradec-6-en-5-one, a tricyclic ketone related to the ophiobolins"}]},{"@id":"https://cir.nii.ac.jp/crid/1362544418558006272","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"The chemical transformation of cephalonic acid"}]},{"@id":"https://cir.nii.ac.jp/crid/1362544419547200000","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Structure and conformation of ophiobolin K and 6- epiophiobolin K from Aspergillus ustus as a nematocidal agent."}]},{"@id":"https://cir.nii.ac.jp/crid/1362544420789569792","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Cytotoxic sesterterpenes, 6-epi-ophiobolin G and 6-epi-ophiobolin N, from marine derived fungus Emericella variecolor GF10"}]},{"@id":"https://cir.nii.ac.jp/crid/1362544420898548224","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Eight membered ethers via diene metathesis: Synthetic approach to laureatin natural products"}]},{"@id":"https://cir.nii.ac.jp/crid/1362825894679802112","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Ophiobolin A, a Novel Apoptosis-inducing Agent from Fungus Strain f-7438"}]},{"@id":"https://cir.nii.ac.jp/crid/1362825894909758080","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A short enantiospecific synthesis of the ceroplastin nucleus."}]},{"@id":"https://cir.nii.ac.jp/crid/1362825895108283648","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Rapid and efficient construction of the ophiobolin nucleus"}]},{"@id":"https://cir.nii.ac.jp/crid/1362825895711293184","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A Concise Total Synthesis of Dactylol via Ring Closing Metathesis"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107368381454208","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Studies toward the total synthesis of di- and sesterterpenes with a dicyclopenta[a,d]cyclooctane skeleton. Construction of a versatile A/B ring building block via a ring-closing metathesis reaction and carbocationic rearrangement"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107368832385280","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"The isolation of an acyclic C25-isoprenoid alcohol, geranylnerolidol, and a new ophiobolin"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107369136864896","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Enantiospecific construction of the BC-ring system of taxanes"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107369535506560","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthesis of BC Ring-Systems of Taxol by Ring-Closing Metathesis"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107369559653376","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"An approach toward the ophiobolane sesterterpenes: synthesis of the ceroplastin nucleus"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107369575067392","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Toward an Analogue of the Transition State of PreD<sub>3</sub>−D<sub>3</sub> Isomerization: Stereoselective Synthesis of Linearly Fused 6-8-6 Carbocyclic Systems<sup>1</sup>"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107369629547136","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Ophiobolins G and H: new fungal metabolites from a novel source, Aspergillus ustus"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107370300079616","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A synthetic entry into the ophiobolane ring system"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107370511197440","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthesis of ‘inside–outside’ medium-sized rings via ring-closing metathesis"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107370962104064","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthetic studies on ophiobolins"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107371336382720","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Toward an Efficient Synthesis of Taxane Analogs by Dienyne Ring-Closing Metathesis"}]},{"@id":"https://cir.nii.ac.jp/crid/1363388843615961856","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Studies Towards the Total Synthesis of Cycloaraneosene and Ophiobolin M: A General Strategy for the Construction of the 5−8 Bicyclic Ring System"}]},{"@id":"https://cir.nii.ac.jp/crid/1363388843952002816","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"The structure of zizannin-A and -B, C25-terpenoids isolated from"}]},{"@id":"https://cir.nii.ac.jp/crid/1363388846031063936","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Microbial Metabolites of Ophiobolin A and Antimicrobial Evaluation of Ophiobolins"}]},{"@id":"https://cir.nii.ac.jp/crid/1363670319057355520","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A route, via tetraquinane, to the 5-8-5 carbocyclic nucleus of fusicoccins and ophiobolins"}]},{"@id":"https://cir.nii.ac.jp/crid/1363670320101170304","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Some new phytotoxic ophiobolins produced by Drechslera oryzae"}]},{"@id":"https://cir.nii.ac.jp/crid/1363670320418884736","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Ophiobolin A. A natural product inhibitor of calmodulin."}]},{"@id":"https://cir.nii.ac.jp/crid/1363670320716583808","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Highly Efficient Ruthenium Catalysts for the Formation of Tetrasubstituted Olefins via Ring-Closing Metathesis"}]},{"@id":"https://cir.nii.ac.jp/crid/1363670320807830016","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"The structure of cephalonic acid, a pentaprenyl terpenoid"}]},{"@id":"https://cir.nii.ac.jp/crid/1363670321210972800","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthesis of model BC bicycles of taxol using C10–C11 ring-closing metathesis strategy"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951793543555840","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A mild oxidizing reagent for alcohols and 1,2-diols: o-iodoxybenzoic acid (IBX) in DMSO"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951794051760896","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"4-exo-dig and 5-exo-dig Cyclocarbopalladations: an expeditious solution toward molecular complexity?"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951795208026624","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Pyridine-derived triflating reagents: An improved preparation of vinyl triflates from metallo enolates."}]},{"@id":"https://cir.nii.ac.jp/crid/1363951795927484800","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Total Synthesis of (±)-Asteriscanolide"}]},{"@id":"https://cir.nii.ac.jp/crid/1364233268274431488","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Fusicoccin Synthesis by Intramolecular [4+4] Photocycloaddition of 2-Pyridones: Stereocontrol of the Cycloaddition and Elaboration of the Pentacyclic Product"}]},{"@id":"https://cir.nii.ac.jp/crid/1364233269289737856","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Isolation and constitution of cochliobolin b"}]},{"@id":"https://cir.nii.ac.jp/crid/1364233269688196992","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"The Structure of Ophiobolin, a C<sub>25</sub> Terpenoid Having a Novel Skeleton"}]},{"@id":"https://cir.nii.ac.jp/crid/1364233270355046400","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Ophiobolin E and 8-epi-ophiobolin J produced by Drechslera gigantea, a potential mycoherbicide of weedy grasses"}]},{"@id":"https://cir.nii.ac.jp/crid/1390001204117143680","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Trialkylborane as an initiator and terminator of free radical reactions. Facile routes to boron enolates via .ALPHA.-carbonyl radicals and aldol reaction of boron enolates."},{"@value":"Trialkylborane as an Initiator and Terminator of Free Radical Reactions. Facile Routes to Boron Enolates via α-Carbonyl Radicals and Aldol Reaction of Boron Enolates"}]},{"@id":"https://cir.nii.ac.jp/crid/1390001204533473280","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@language":"en","@value":"On the New Antibiotics “Ophiobolin”, produced by <i>Ophiobolus Mi0yabeanus</i>"},{"@value":"稲胡麻葉枯病菌の生産する新抗生物質(オフィオボリン)について"}]},{"@id":"https://cir.nii.ac.jp/crid/1390021615648036736","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Total Synthesis of Natural Products Full of Surprises and Emotion"},{"@language":"ja","@value":"驚きと感動に満ちた天然物の全合成"}]},{"@id":"https://cir.nii.ac.jp/crid/2050025942155224064","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Research on the efficient enantioselective total synthesis of useful bioactive polycyclic compounds"}]}],"dataSourceIdentifier":[{"@type":"CROSSREF","@value":"10.1002/anie.201104447"},{"@type":"CROSSREF","@value":"10.1002/ange.201104447"},{"@type":"KAKEN","@value":"PRODUCT-12504263"},{"@type":"OPENAIRE","@value":"doi_dedup___::393becf31448f585bd5583cd940327be"},{"@type":"CROSSREF","@value":"10.1002/chem.201204119_references_DOI_5C8TPuavpbyXJDMtTJxzw69npn7"},{"@type":"CROSSREF","@value":"10.1002/chem.201204119_references_DOI_HiNVclAKb34Jw7i3m3Ot3GzSGDC"},{"@type":"CROSSREF","@value":"10.1016/j.tet.2012.12.014_references_DOI_HiNVclAKb34Jw7i3m3Ot3GzSGDC"},{"@type":"CROSSREF","@value":"10.1246/bcsj.20210329_references_DOI_HiNVclAKb34Jw7i3m3Ot3GzSGDC"},{"@type":"CROSSREF","@value":"10.5059/yukigoseikyokaishi.83.156_references_DOI_HiNVclAKb34Jw7i3m3Ot3GzSGDC"},{"@type":"CROSSREF","@value":"10.1016/j.tetlet.2017.01.076_references_DOI_HiNVclAKb34Jw7i3m3Ot3GzSGDC"},{"@type":"CROSSREF","@value":"10.1021/ol500654g_references_DOI_HiNVclAKb34Jw7i3m3Ot3GzSGDC"},{"@type":"CROSSREF","@value":"10.1016/j.tetlet.2021.153608_references_DOI_HiNVclAKb34Jw7i3m3Ot3GzSGDC"},{"@type":"CROSSREF","@value":"10.1021/jacs.0c01774_references_DOI_HiNVclAKb34Jw7i3m3Ot3GzSGDC"},{"@type":"CROSSREF","@value":"10.1021/cr500716f_references_DOI_HiNVclAKb34Jw7i3m3Ot3GzSGDC"},{"@type":"CROSSREF","@value":"10.1016/j.tetasy.2013.01.019_references_DOI_HiNVclAKb34Jw7i3m3Ot3GzSGDC"}]}