{"@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/1363388844871639808.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1021/jo00399a052"}},{"identifier":{"@type":"URI","@value":"https://pubs.acs.org/doi/pdf/10.1021/jo00399a052"}}],"dc:title":[{"@value":"Synthesis of .alpha.,.beta.-unsaturated carbonyl compounds by palladium(II)-catalyzed dehydrosilylation of silyl enol ethers"}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1383388844871639809","@type":"Researcher","foaf:name":[{"@value":"Yoshihiko Ito"}]},{"@id":"https://cir.nii.ac.jp/crid/1383388844871639810","@type":"Researcher","foaf:name":[{"@value":"Toshikazu Hirao"}]},{"@id":"https://cir.nii.ac.jp/crid/1383388844871639808","@type":"Researcher","foaf:name":[{"@value":"Takeo Saegusa"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"00223263"},{"@type":"EISSN","@value":"15206904"}],"prism:publicationName":[{"@value":"The Journal of Organic Chemistry"}],"dc:publisher":[{"@value":"American Chemical Society (ACS)"}],"prism:publicationDate":"1978-03","prism:volume":"43","prism:number":"5","prism:startingPage":"1011","prism:endingPage":"1013"},"reviewed":"false","url":[{"@id":"https://pubs.acs.org/doi/pdf/10.1021/jo00399a052"}],"createdAt":"2005-03-12","modifiedAt":"2023-04-07","relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1050001202655184768","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Synthetic studies toward aplysiasecosterol A: Construction of the novel tricyclic core"}]},{"@id":"https://cir.nii.ac.jp/crid/1050001202731751040","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Development and Application of a Convergent Strategy for the Total Synthesis of Polycyclic Ether Natural Products"}]},{"@id":"https://cir.nii.ac.jp/crid/1050282677545623424","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis of 2,2-Di-C-methyl-2-deoxy- and 4,4-Di-C-methyl-4-deoxypyranosides via Michael Addition of Conjugated Enopyranosiduloses"}]},{"@id":"https://cir.nii.ac.jp/crid/1050282677610870784","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Total synthesis of natural derivatives and artificial analogs of 13-oxyingenol and their biological evaluation"}]},{"@id":"https://cir.nii.ac.jp/crid/1050564288759320576","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"De Novo Synthesis of Possible Candidates for the Inagami–Tamura Endogenous Digitalis-like Factor"}]},{"@id":"https://cir.nii.ac.jp/crid/1360002214425965824","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Stereospecificity in Intramolecular Photoredox Reactions of Naphthoquinones: Enantioselective Total Synthesis of (−)‐Spiroxin C"}]},{"@id":"https://cir.nii.ac.jp/crid/1360002216658399104","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Design and Synthesis of Skeletal Analogues of Gambierol: Attenuation of Amyloid-β and Tau Pathology with Voltage-Gated Potassium Channel and<i>N</i>-Methyl-<scp>d</scp>-aspartate Receptor Implications"}]},{"@id":"https://cir.nii.ac.jp/crid/1360002219107421440","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"SYNTHESIS OF ENAMINONES BY Pd(II) INDUCED DEHYDROGENATION OF β-AMINO KETONES"}]},{"@id":"https://cir.nii.ac.jp/crid/1360002219107542656","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"STEREOCONTROLLED SYNTHESIS OF TRICYCLO[6.2.1.04.9]UNDECANE RING SYSTEM OF ACONITIUM ALKALOIDS"}]},{"@id":"https://cir.nii.ac.jp/crid/1360002219108236928","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Structure Elucidation of “Hydroxycycloaraneosene” by Unambiguous Total Synthesis. An Eight-Membered Ring Formation via a Lewis Acid-Catalyzed Ene-Reaction"}]},{"@id":"https://cir.nii.ac.jp/crid/1360004229916374400","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Catalytic Asymmetric Total Synthesis of <i>ent</i>‐Hyperforin"}]},{"@id":"https://cir.nii.ac.jp/crid/1360004229945818240","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Asymmetric Total Synthesis of (−)‐Lundurine B and Determination of Its Absolute Stereochemistry"}]},{"@id":"https://cir.nii.ac.jp/crid/1360004233249250560","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Total Synthesis of (±)-Kainic Acid: A Photochemical C–H Carbamoylation Approach"}]},{"@id":"https://cir.nii.ac.jp/crid/1360004233249349760","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Oxidative Conversion of Silyl Enol Ethers to α,β-Unsaturated Ketones Employing Oxoammonium Salts"}]},{"@id":"https://cir.nii.ac.jp/crid/1360004233408948224","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Furan-iminium cation cyclization (FIC) in a total synthesis of manzamine alkaloids"}]},{"@id":"https://cir.nii.ac.jp/crid/1360006529434556928","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthetic Studies toward Aplysiasecosterol A: Concise Synthesis of the Tricyclic Core and Its Reactions for Introduction of the D Ring Fragment"}]},{"@id":"https://cir.nii.ac.jp/crid/1360009142694542208","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Unified Total Synthesis of Five Bufadienolides"}]},{"@id":"https://cir.nii.ac.jp/crid/1360009142902271104","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthetic Study on Lactonamycins, Part 2: Stereoselective Access to ABCD-Ring System"}]},{"@id":"https://cir.nii.ac.jp/crid/1360013172154750848","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Stereochemical Dichotomy in Two Competing Cascade Processes: Total Syntheses of Both Enantiomers of Spiroxin A"}]},{"@id":"https://cir.nii.ac.jp/crid/1360021394480025856","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Convergent and Scalable Synthesis of the ABCDE-Ring Fragment of Caribbean Ciguatoxin C-CTX-1"}]},{"@id":"https://cir.nii.ac.jp/crid/1360283689443187840","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Practical Route to the Left Wing of CTX1B and Total Syntheses of CTX1B and 54‐deoxyCTX1B"}]},{"@id":"https://cir.nii.ac.jp/crid/1360283691852329728","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Visible-light-mediated addition of α-aminoalkyl radicals generated from α-silylamines to α,β-unsaturated carbonyl compounds"}]},{"@id":"https://cir.nii.ac.jp/crid/1360283694079740544","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthetic Photochemistry. XLII. Total Synthesis of Cycloaraneosene, a Fundamental Hydrocarbon of 5–8–5-Membered Tricydic Diterpenoid from <i>Sordaria araneosa</i>"}]},{"@id":"https://cir.nii.ac.jp/crid/1360283694080057728","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"The Total Synthesis of 8β-Hydroxycycloaraneosene by Means of an Eight-Membered Ring-Formation via a Lewis Acid-Catalyzed Ene Reaction. Confirmation of Its Natural Occurrence"}]},{"@id":"https://cir.nii.ac.jp/crid/1360283694081802752","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Development of Catalytic Enantioselective Reactions via Palladium Enolates as Key Intermediates"}]},{"@id":"https://cir.nii.ac.jp/crid/1360283694083922432","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"A NEW METHOD FOR THE DIRECT INTRODUCTION OF ALKOXYL GROUP TO SILYL ENOL ETHER WITH ALKYL HYPOCHLORITE CATALYZED BY PALLADIUM(O)"}]},{"@id":"https://cir.nii.ac.jp/crid/1360283694084442880","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Total Synthesis of Cycloaraneosene, a Fundamental Hydrocarbon of “epi”-Fusicoccane Diterpenoids, and the Structure Revision of Its Congener, Hydroxycycloaraneosene"}]},{"@id":"https://cir.nii.ac.jp/crid/1360283694088472832","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"β-Amination of Saturated Nitriles through Palladium-catalyzed Dehydrogenation, 1,4-Addition, and Re-dehydrogenation"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285704894973952","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Total Synthesis of (−)‐13‐Oxyingenol and its Natural Derivative"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285704897292416","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"A Concise and Versatile Synthesis of Alkaloids from <i>Kopsia tenuis</i>: Total Synthesis of (±)‐Lundurine A and B"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285704920968960","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthetic Studies of the Zoanthamine Alkaloids: Total Synthesis of Zoanthenol Based on an Isoaromatization Strategy"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285707503922560","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"First total synthesis of (±)-adunctin B"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285708133393024","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Total Synthesis of Zoanthamine Alkaloids"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285708206458240","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Three Different Dimerizations of 2-Bromo-3-methyl-1,4-naphthoquinones"}]},{"@id":"https://cir.nii.ac.jp/crid/1360298755633564544","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Total Synthesis of Aculenes B and D"}]},{"@id":"https://cir.nii.ac.jp/crid/1360302865555848832","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Total Synthesis of Aplysiasecosterols A and B, Two Marine 9,11-Secosteroids"}]},{"@id":"https://cir.nii.ac.jp/crid/1360565164418618368","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Total Synthesis of Gambierol by Using Oxiranyl Anions"}]},{"@id":"https://cir.nii.ac.jp/crid/1360565166132050304","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Recent topics in total syntheses of natural dimeric naphthoquinone derivatives"}]},{"@id":"https://cir.nii.ac.jp/crid/1360565166611662592","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Enantiocontrolled Total Syntheses of Breviones A, B, and C"}]},{"@id":"https://cir.nii.ac.jp/crid/1360565166635874816","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Total Synthesis of Gambierol"}]},{"@id":"https://cir.nii.ac.jp/crid/1360565169050547712","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Total Syntheses of the Non-Peptide Bradykinin B1 Receptor Antagonist Velutinol A and Its Analogs,<i>seco</i>-Pregnanes with a Cage-Like Moiety"}]},{"@id":"https://cir.nii.ac.jp/crid/1360565169060498176","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"PALLADIUM-PROMOTED REACTION OF ALLYL TRIMETHYLSILYL ETHERS WITH ARYL IODIDES"}]},{"@id":"https://cir.nii.ac.jp/crid/1360565169060618880","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"PALLADIUM-PROMOTED TRANSFORMATION OF α,β-EPOXYSILANES TO α,β-UNSATURATED CARBONYL COMPOUNDS"}]},{"@id":"https://cir.nii.ac.jp/crid/1360565169062551680","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Preparation of (+)-Tricyclo[6.2.1.02,7]undec-2(7)-en-3-one and Its Conversion into (+)-<i>epi</i>-<i>β</i>-Santalene"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567179876214656","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Total Syntheses of (+)‐Grandilodine C and (+)‐Lapidilectine B and Determination of their Absolute Stereochemistry"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567183182964736","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Catalytic Enantioselective Total Synthesis of (−)-Platyphyllide and Its Structural Revision"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567183554323200","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"A convergent total synthesis of ouabagenin"}]},{"@id":"https://cir.nii.ac.jp/crid/1360846644026923776","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Total Synthesis of Structurally Complex Marine Oxacyclic Natural Products"}]},{"@id":"https://cir.nii.ac.jp/crid/1360846644033015424","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Preparation of Bicyclo[3.3.1]nonane-2,4-dione Derivatives"}]},{"@id":"https://cir.nii.ac.jp/crid/1360846644033887744","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"The Palladium–Catalyzed Cross-Coupling Reaction of Enol Acetates of α-Bromo Ketones with 1-Alkenyl-, Aryl-, or Alkylboron Compounds; A Facile Synthesis of Ketones and Their Enol Acetates"}]},{"@id":"https://cir.nii.ac.jp/crid/1360846644037408384","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"THE DIRECT SYNTHESIS OF α,β-UNSATURATED CARBONYL COMPOUNDS BY Pd(II) PROMOTED DEHYDROGENATION OF ALDEHYDES AND KETONES"}]},{"@id":"https://cir.nii.ac.jp/crid/1360846644039906816","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"A New and One-Pot Synthesis of α,β-Unsaturated Ketones by Dehydrogenation of Various Ketones with <i>N-tert</i>-Butyl Phenylsulfinimidoyl Chloride"}]},{"@id":"https://cir.nii.ac.jp/crid/1360846645767640448","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Total Synthesis of Gambierol"}]},{"@id":"https://cir.nii.ac.jp/crid/1360848658060862976","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Diastereoselective Ring-Closing Metathesis as a Means to Construct Medium-Sized Cyclic Ethers: Application to the Synthesis of a Photoactivatable Gambierol Derivative"}]},{"@id":"https://cir.nii.ac.jp/crid/1360848658061539328","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Total Synthesis and Biological Evaluation of 19-Hydroxysarmentogenin-3<i>-O</i>-α-<scp>l</scp>-rhamnoside, Trewianin, and Their Aglycons"}]},{"@id":"https://cir.nii.ac.jp/crid/1360848658159770880","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Total Synthesis of Optically Active Lycopladine A by Utilizing Diastereoselective Protection of Carbonyl Group in a 1,3-Cyclohexanedione Derivative"}]},{"@id":"https://cir.nii.ac.jp/crid/1360848658179350656","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthetic Studies toward 13-Oxyingenol: Construction of the Fully Substituted Tetracyclic Compound"}]},{"@id":"https://cir.nii.ac.jp/crid/1360848658179624064","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Total Synthesis of (+)-<i>trans</i>-Dihydronarciclasine Utilizing Asymmetric Conjugate Addition"}]},{"@id":"https://cir.nii.ac.jp/crid/1360849942947588480","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"CeO<sub>2</sub>-Supported Pd(II)-on-Au Nanoparticle Catalyst for Aerobic Selective α,β-Desaturation of Carbonyl Compounds Applicable to Cyclohexanones"}]},{"@id":"https://cir.nii.ac.jp/crid/1360853567624608256","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Construction of the ABCE-ring structure of talatisamine via decarboxylative radical cyclization"}]},{"@id":"https://cir.nii.ac.jp/crid/1390001204120101248","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Synthetic strategy of 5-8-5-membered tricyclic higher terpenoids based on the condensation of two optically-active iridoids, C10-synthons obtained from photo-cycloadduct of methyl 2,4-dioxopentanoate-isoprene, and its application to a synthesis of the basic carbon skeleton of fusicoccane."},{"@value":"Synthetic Photochemistry. XXXIV. Synthetic Strategy of 5-8-5-Membered Tricyclic Higher Terpenoids Based on the Condensation of Two Optically-Active Iridoids, C10-Synthons Obtained from Photo-Cycloadduct of Methyl 2,4-Dioxopentanoate–Isoprene, and Its Application to a Synthesis of the Basic Carbon Skeleton of Fusicoccane"}]},{"@id":"https://cir.nii.ac.jp/crid/1390001204128456960","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Palladium-promoted transformation of .BETA.-amino ketones to enaminones."},{"@value":"Palladium-Promoted Transformation of β-Amino Ketones to Enaminones"}]},{"@id":"https://cir.nii.ac.jp/crid/1390001204577416448","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"SYNTHESIS OF FUSICOCCA-2,8,10-TRIENE, A BIOGENETIC MISSING LINK, STARTING FROM STEREOSPECIFIC CONDENSATION OF TWO IRIDOID SYNTHONS"}]},{"@id":"https://cir.nii.ac.jp/crid/1390001205339533312","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Synthesis of Halichlorine"},{"@language":"ja","@value":"ハリクロリンの合成"},{"@language":"ja-Kana","@value":"ハリクロリン ノ ゴウセイ"}]},{"@id":"https://cir.nii.ac.jp/crid/1390001205339988096","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Development of Catalytic and Enantioselective Diels-Alder Reaction of Electron-Rich Dienes Using Chiral Rare-Earth Metal Complex"},{"@language":"ja","@value":"光学活性希土類錯体を用いる電子豊富ジエンの触媒的不斉Diels-Alder反応の開発"},{"@language":"ja-Kana","@value":"コウガク カッセイキドルイ サクタイ オ モチイル デンシ ホウフ ジエン ノ ショクバイテキ フセイ Diels-Alder ハンノウ ノ カイハツ"}]},{"@id":"https://cir.nii.ac.jp/crid/1390001205340427264","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"ja","@value":"ゾアンタミンアルカロイドの化学合成"},{"@language":"en","@value":"Chemical Synthesis of Zoanthamine Alkaloids"},{"@language":"ja-Kana","@value":"ゾアンタミンアルカロイド ノ カガク ゴウセイ"}]},{"@id":"https://cir.nii.ac.jp/crid/1390282679105444608","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Rearrangement approaches to cyclic skeletons. III. Practical route to cis-bicyclo(4.3.0)non-4-en-7-ones based on photochemical (1,3) acyl migration of bicyclo(3.2.2)non-6-en-2-ones."},{"@value":"Rearrangement Approaches to Cyclic Skeletons. III. Practical Route to <i>cis</i>-Bicyclo[4.3.0]non-4-en-7-ones Based on Photochemical [1,3] Acyl Migration of Bicyclo[3.2.2]non-6-en-2-ones"}]},{"@id":"https://cir.nii.ac.jp/crid/1390282680316296192","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Development of Biofunctional Molecules Based on Total Synthesis of Natural Products"},{"@language":"ja","@value":"生物活性天然物の全合成を起点とした生体機能分子創製への展開"}]},{"@id":"https://cir.nii.ac.jp/crid/1390282680316700928","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Total Synthesis of Cortistatin A and J"},{"@language":"ja","@value":"コルチスタチンの全合成"},{"@language":"ja-Kana","@value":"コルチスタチン ノ ゼン ゴウセイ"}]},{"@id":"https://cir.nii.ac.jp/crid/1390282681104280704","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"ja","@value":"キナマイシン系抗生物質の全合成研究"},{"@language":"en","@value":"Synthetic Studies towards Kinamycin Antibiotics"},{"@language":"ja-Kana","@value":"キナマイシンケイ コウセイブツシツ ノ ゼンゴウセイ ケンキュウ"},{"@value":"ChemInform Abstract: Synthetic Studies Towards Kinamycin Antibiotics"}]},{"@id":"https://cir.nii.ac.jp/crid/1390282763081640704","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Development of New Synthetic Methods Using Oxiranyl Anions and Application in the Syntheses of Polycyclic Ether Marine Natural Products"}]},{"@id":"https://cir.nii.ac.jp/crid/1390283659869506560","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Total Syntheses of Structurally Complex Natural Products: Potential Reactivity of Organic Molecules"},{"@language":"ja","@value":"有機分子の潜在的反応性を活用した高次構造天然物の全合成研究"},{"@language":"ja-Kana","@value":"ユウキ ブンシ ノ センザイテキ ハンノウセイ オ カツヨウ シタ コウジ コウゾウ テンネンブツ ノ ゼン ゴウセイ ケンキュウ"}]},{"@id":"https://cir.nii.ac.jp/crid/1390288912170012032","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Synthetic Study of Polycyclic Natural Products Based on Development of New Strategy"},{"@language":"ja","@value":"新規反応開発を基盤とする多環性天然物合成"},{"@language":"ja-Kana","@value":"シンキ ハンノウ カイハツ オ キバン ト スル タカンセイ テンネンブツ ゴウセイ"}]},{"@id":"https://cir.nii.ac.jp/crid/1390302459085621248","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Total Synthesis of Fused Natural Products"},{"@language":"ja","@value":"縮環型天然物の全合成"}]},{"@id":"https://cir.nii.ac.jp/crid/1390564237996753536","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"ja","@value":"ランドリンおよび類縁体の全合成"},{"@language":"en","@value":"Total Synthesis of Lundurines and Related Alkaloids"},{"@language":"ja-Kana","@value":"ランドリン オヨビ ルイエンタイ ノ ゼン ゴウセイ"},{"@value":"Total Synthesis of Lundurine and Related Alkaloids"}]},{"@id":"https://cir.nii.ac.jp/crid/1390564238090736128","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Convergent Total Synthesis of Bioactive Cardenolides"},{"@language":"ja","@value":"生物活性カルデノリド類の収束的全合成"},{"@language":"ja-Kana","@value":"セイブツ カッセイ カルデノリドルイ ノ シュウソクテキ ゼン ゴウセイ"}]},{"@id":"https://cir.nii.ac.jp/crid/1390845702318369792","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Synthetic Studies of Polycyclic Terpenoids Using the Intramolecular Aldol-Type Cyclization Reaction"}]},{"@id":"https://cir.nii.ac.jp/crid/1390848647560064640","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Catalytic Synthesis of Optically Active Polycyclic Heterocyclic Compounds"},{"@language":"ja","@value":"光学活性多環性複素環骨格の触媒的合成法の開発"},{"@value":"Review for award 光学活性多環性複素環骨格の触媒的合成法の開発"},{"@language":"ja-Kana","@value":"Review for award コウガク カッセイ タカンセイフクソカン コッカク ノ ショクバイテキ ゴウセイホウ ノ カイハツ"}]},{"@id":"https://cir.nii.ac.jp/crid/1520291855860046848","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"光学活性希土類錯体を用いる高度分子変換"},{"@language":"ja-Kana","@value":"コウガク カッセイキドルイ サクタイ オ モチイル コウド ブンシ ヘンカン"}]},{"@id":"https://cir.nii.ac.jp/crid/2051714792001896192","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Convergent syntheses of the WXYZ ring of maitotoxin and the HIJK ring of brevisulcenal-F"}]},{"@id":"https://cir.nii.ac.jp/crid/2051996266990313600","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Palladium-catalyzed dehydrogenative [3+3] aromatization of propyl ketones and allyl carbonates"}]}],"dataSourceIdentifier":[{"@type":"CROSSREF","@value":"10.1021/jo00399a052"},{"@type":"CROSSREF","@value":"10.1002/anie.201705562_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1002/anie.200906678_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1002/asia.201403407_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1038/ja.2016.24_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1021/acscatal.0c00277_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/bcsj.60.3285_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/bcsj.59.1109_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.5059/yukigoseikyokaishi.71.818_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.5059/yukigoseikyokaishi.71.768_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/cl.1984.1495_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/bcsj.20190048_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.0c03251_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1055/s-0040-1707198_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.5059/yukigoseikyokaishi.76.668_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/cl.220032_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.5059/yukigoseikyokaishi.82.1184_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1021/acs.joc.2c02414_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1002/chem.201405629_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1039/c2cc32745g_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1002/anie.201201383_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1002/anie.201400464_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1002/asia.201000552_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1021/ja300565t_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1016/j.tetlet.2017.07.036_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1021/jo1003746_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1021/ol9017408_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.5059/yukigoseikyokaishi.69.1006_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.5059/yukigoseikyokaishi.72.126_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1021/ja202874d_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1021/ol200772f_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1021/ol2029417_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1248/cpb.c18-00699_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1016/bs.alkal.2017.01.001_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1021/jo200418y_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/bcsj.61.3231_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1002/ejoc.202201482_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.3c01692_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1002/chem.201000497_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1002/anie.201510561_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1039/c5sc00212e_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1039/c6ob02268e_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/cl.2000.1250_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1248/yakushi.20-00137_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1002/anie.201906762_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1021/acs.joc.7b01640_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/bcsj.78.941_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/bcsj.65.2863_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/cl.1995.95_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/bcsj.20100209_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.5059/yukigoseikyokaishi.77.452_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/bcsj.20200401_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1248/yakushi.21-00054_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1016/j.tetlet.2011.10.018_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/bcsj.80.856_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1021/ar200267a_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/cl.1986.1989_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/cl.2013.40_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/cl.1983.1207_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/bcsj.60.1433_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1016/j.tet.2020.131385_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/cl.171056_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.5059/yukigoseikyokaishi.71.124_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/bcsj.59.539_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1248/yakushi.130.1535_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1021/jo300696m_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1021/ol302757y_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/cl.1981.403_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/cl.1984.1419_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/cl.1985.1127_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/cl.1982.1997_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1021/acs.joc.8b02219_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1021/ol103151k_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1021/acs.joc.6b01302_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/cl.1982.369_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/bcsj.60.4369_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.5059/yukigoseikyokaishi.78.304_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1016/j.tetlet.2017.12.040_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1016/j.tetlet.2011.03.119_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/bcsj.63.1729_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.1246/cl.1989.91_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.5059/yukigoseikyokaishi.77.1086_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"},{"@type":"CROSSREF","@value":"10.3987/rev-10-676_references_DOI_U5KS7oFrgwWAfUDvq0z1n7oljFU"}]}