{"@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/1360004233142523264.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1021/acs.orglett.7b03767"}},{"identifier":{"@type":"URI","@value":"https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.7b03767"}}],"resourceType":"学術雑誌論文(journal article)","dc:title":[{"@value":"Heterogeneous Heterobimetallic Catalysis Enabling Expeditious Access to CF<sub>3</sub>-Containing <i>vic</i>-Amino Alcohols"}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1380004233142523265","@type":"Researcher","foaf:name":[{"@value":"Tomoya Karasawa"}],"jpcoar:affiliationName":[{"@value":"Institute of Microbial Chemistry (BIKAKEN), Tokyo, 3-14-23\rKamiosaki, Shinagawa-ku, Tokyo 141-0021, Japan"}]},{"@id":"https://cir.nii.ac.jp/crid/1420564276185170432","@type":"Researcher","personIdentifier":[{"@type":"KAKEN_RESEARCHERS","@value":"40431887"},{"@type":"NRID","@value":"1000040431887"},{"@type":"NRID","@value":"9000370745259"},{"@type":"NRID","@value":"9000391968597"},{"@type":"NRID","@value":"9000410336118"},{"@type":"NRID","@value":"9000304611164"},{"@type":"NRID","@value":"9000391962645"},{"@type":"NRID","@value":"9000391962670"},{"@type":"NRID","@value":"9000409185393"},{"@type":"NRID","@value":"9000009592362"},{"@type":"NRID","@value":"9000257962692"},{"@type":"NRID","@value":"9000402908665"},{"@type":"NRID","@value":"9000288542962"},{"@type":"NRID","@value":"9000391968377"},{"@type":"NRID","@value":"9000391967945"},{"@type":"NRID","@value":"9000403424042"},{"@type":"NRID","@value":"9000018890578"},{"@type":"NRID","@value":"9000283563791"},{"@type":"NRID","@value":"9000241741956"},{"@type":"NRID","@value":"9000019154433"},{"@type":"NRID","@value":"9000301743604"},{"@type":"NRID","@value":"9000021111433"},{"@type":"NRID","@value":"9000415352076"},{"@type":"NRID","@value":"9000391960888"},{"@type":"NRID","@value":"9000345423499"},{"@type":"NRID","@value":"9000404845346"},{"@type":"NRID","@value":"9000272989419"},{"@type":"RESEARCHMAP","@value":"https://researchmap.jp/nkkkn"}],"foaf:name":[{"@value":"Naoya Kumagai"}],"jpcoar:affiliationName":[{"@value":"Institute of Microbial Chemistry (BIKAKEN), Tokyo, 3-14-23\rKamiosaki, Shinagawa-ku, Tokyo 141-0021, Japan"}]},{"@id":"https://cir.nii.ac.jp/crid/1380004233142523264","@type":"Researcher","foaf:name":[{"@value":"Masakatsu Shibasaki"}],"jpcoar:affiliationName":[{"@value":"Institute of Microbial Chemistry (BIKAKEN), Tokyo, 3-14-23\rKamiosaki, Shinagawa-ku, Tokyo 141-0021, Japan"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"15237060"},{"@type":"EISSN","@value":"15237052"}],"prism:publicationName":[{"@value":"Organic Letters"}],"dc:publisher":[{"@value":"American Chemical Society (ACS)"}],"prism:publicationDate":"2017-12-26","prism:volume":"20","prism:number":"1","prism:startingPage":"308","prism:endingPage":"311"},"reviewed":"false","url":[{"@id":"https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.7b03767"}],"createdAt":"2017-12-26","modifiedAt":"2023-04-24","project":[{"@id":"https://cir.nii.ac.jp/crid/1040000781894347392","@type":"Project","projectIdentifier":[{"@type":"KAKEN","@value":"16H01043"},{"@type":"JGN","@value":"JP16H01043"},{"@type":"URI","@value":"https://kaken.nii.ac.jp/grant/KAKENHI-PUBLICLY-16H01043/"}],"notation":[{"@language":"ja","@value":"アルキルニトリルの汎用炭素求核剤としての利用を可能にする新規触媒系の開拓"},{"@language":"en","@value":"Development of Catalytic Asymmetric C–C Bond-Forming Reactions Using Alkylnitriles as Pronucleophiles"}]},{"@id":"https://cir.nii.ac.jp/crid/1040000781956306432","@type":"Project","projectIdentifier":[{"@type":"KAKEN","@value":"17H03025"},{"@type":"JGN","@value":"JP17H03025"},{"@type":"URI","@value":"https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-17H03025/"}],"notation":[{"@language":"ja","@value":"協奏機能型触媒が拓くサステイナブルな直截型反応群の開発"},{"@language":"en","@value":"Development of Sustainable Chemical Reactions Driven by Designed Cooperative Catalysts"}]}],"relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1360002216659233536","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"<i>anti</i>-Selective Catalytic Asymmetric Nitroaldol Reaction via a Heterobimetallic Heterogeneous Catalyst"}]},{"@id":"https://cir.nii.ac.jp/crid/1360004232527861504","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Preparation of Nd/Na heterogeneous catalyst from bench-stable and inexpensive Nd salt for an anti-selective catalytic asymmetric nitroaldol reaction"}]},{"@id":"https://cir.nii.ac.jp/crid/1360004233142900352","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Solvent-Dependent Enantiodivergence in<i>anti</i>-Selective Catalytic Asymmetric Nitroaldol Reactions"}]},{"@id":"https://cir.nii.ac.jp/crid/1360004233249779328","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Self-Assembled Asymmetric Catalyst Engaged in a Continuous-Flow Platform: An<i>Anti</i>-Selective Catalytic Asymmetric Nitroaldol Reaction"}]},{"@id":"https://cir.nii.ac.jp/crid/1360004236988361344","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Robust Continuous-Flow Synthesis of Deuterium-Labeled <i>β</i>-Nitroalcohols Catalyzed by Basic Anion Exchange Resin"}]},{"@id":"https://cir.nii.ac.jp/crid/1360011144217224704","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Stereodivergent Catalytic Doubly Diastereoselective Nitroaldol Reactions Using Heterobimetallic Complexes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360283689384931840","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Catalytic Asymmetric Synthesis of α‐Trifluoromethylated Carbinols: A Case Study of Tertiary Propargylic Alcohols"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285704894652800","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Catalytic Asymmetric <i>anti</i>‐Selective Nitroaldol Reaction En Route to Zanamivir"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285708751472640","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Design of a Chiral Secondary Amine Ligand for Copper-Catalyzed anti-Selective Henry Reaction"}]},{"@id":"https://cir.nii.ac.jp/crid/1360292617907821440","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Fluorine in medicinal chemistry"}]},{"@id":"https://cir.nii.ac.jp/crid/1360292618946087296","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"<i>syn</i>‐ and Enantioselective Henry Reactions of Aliphatic Aldehydes and Application to the Synthesis of Safingol"}]},{"@id":"https://cir.nii.ac.jp/crid/1360292619216498432","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Practical Asymmetric Henry Reaction Catalyzed by a Chiral Diamine-Cu(OAc)<sub>2</sub> Complex"}]},{"@id":"https://cir.nii.ac.jp/crid/1360292621083490944","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Development of New N,N-Ligands for the Enantioselective Copper(II)-Catalyzed Henry Reaction"}]},{"@id":"https://cir.nii.ac.jp/crid/1360294643778280704","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Asymmetric Henry Reaction of Trifluoromethyl Enones with Nitromethane Using a <i>N,N</i>‐Dibenzyl Diaminomethylenemalononitrile Organocatalyst"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567183170741120","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"<i>anti</i>-Selective Catalytic Asymmetric Nitroaldol Reaction of α-Keto Esters: Intriguing Solvent Effect, Flow Reaction, and Synthesis of Active Pharmaceutical Ingredients"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567183183345792","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A Modified Preparation Procedure for Carbon Nanotube-Confined Nd/Na Heterobimetallic Catalyst for <i>anti</i>-Selective Catalytic Asymmetric Nitroaldol Reactions"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574092890370048","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Next Generation of Fluorine-Containing Pharmaceuticals, Compounds Currently in Phase II–III Clinical Trials of Major Pharmaceutical Companies: New Structural Trends and Therapeutic Areas"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574093724980224","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Enantioselective Henry Reaction Catalyzed by Cu<sup>II</sup> Salt and Bipiperidine"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574094206361216","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Promotion of Henry reactions using Cu(OTf)2 and a sterically hindered Schiff base: access to enantioenriched β-hydroxynitroalkanes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574094767835648","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A New Class of Urea-Substituted Cinchona Alkaloids Promote Highly Enantioselective Nitroaldol reactions of Trifluoromethylketones"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574095727431040","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Organocatalytic Asymmetric Nitroaldol Reaction: Cooperative Effects of Guanidine and Thiourea Functional Groups"}]},{"@id":"https://cir.nii.ac.jp/crid/1360580230600393728","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Highly efficient, asymmetric, and organocatalyst-based Henry reactions between α,β-unsaturated trifluoromethyl ketone and nitromethane"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855570541122176","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Basic character of rare earth metal alkoxides. Utilization in catalytic carbon-carbon bond-forming reactions and catalytic asymmetric nitroaldol reactions"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855571018914560","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A Highly <i>anti</i>‐Selective Asymmetric Henry Reaction Catalyzed by a Chiral Copper Complex: Applications to the Syntheses of (+)‐Spisulosine and a Pyrroloisoquinoline Derivative"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855571074611200","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Copper Complex of Aminoisoborneol Schiff Base Cu<sub>2</sub>(SBAIB‐d)<sub>2</sub>: An Efficient Catalyst for Direct Catalytic Asymmetric Nitroaldol (Henry) Reaction"}]},{"@id":"https://cir.nii.ac.jp/crid/1361137044636992384","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Diastereoselective and Enantioselective Henry (Nitroaldol) Reaction Utilizing a Guanidine‐Thiourea Bifunctional Organocatalyst"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418519774574336","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Asymmetric catalysis for the construction of quaternary carbon centres: nucleophilic addition on ketones and ketimines"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418520726975744","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A Heterobimetallic Pd/La/Schiff Base Complex for <i>anti</i>‐Selective Catalytic Asymmetric Nitroaldol Reactions and Applications to Short Syntheses of β‐Adrenoceptor Agonists"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418520893755136","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Asymmetric Henry reaction of trifluoromethyl ketone and aldehyde using Cu(II)-complex: computational study offers the origin of enantioselectivity with varied size of catalysts"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699993978333568","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Chiral Tetraaminophosphonium Salt-Mediated Asymmetric Direct Henry Reaction"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699995053250944","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A Highly Diastereo- and Enantioselective Copper(I)-Catalyzed Henry Reaction Using a Bis(sulfonamide)−Diamine Ligand"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981468405977600","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Self‐Assembling Neodymium/Sodium Heterobimetallic Asymmetric Catalyst Confined in a Carbon Nanotube Network"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981468451457152","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"<i>anti</i>-Selective Asymmetric Henry Reaction Catalyzed by a Heterobimetallic Cu–Sm–Aminophenol Sulfonamide Complex"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981469055969280","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Enantioselective organocatalyzed Henry reaction with fluoromethyl ketones"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981470532144000","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Catalytic Enantioselective Construction of All-Carbon Quaternary Stereocenters"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981471378086016","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthesis of β-amino-α-trifluoromethyl alcohols and their applications in organic synthesis"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262943375857664","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Efficient Asymmetric Copper(I)‐Catalyzed Henry Reaction Using Chiral <i>N</i>‐Alkyl‐<i>C</i><sub>1</sub>‐tetrahydro‐1,1′‐bisisoquinolines"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262943956798848","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A catalytic asymmetric anti-selective nitroaldol reaction with a neodymium–sodium heterobimetallic complex"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262944015800320","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"The Catalytic Enantioselective Construction of Molecules with Quaternary Carbon Stereocenters"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262945033135232","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Recent Advances in the Catalytic Asymmetric Nitroaldol (Henry) Reaction"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262946016313088","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Fluorine in Pharmaceuticals: Looking Beyond Intuition"}]},{"@id":"https://cir.nii.ac.jp/crid/1362544418407110656","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Asymmetric <i>Syn</i>-Selective Henry Reaction Catalyzed by the Sulfonyldiamine−CuCl−Pyridine System"}]},{"@id":"https://cir.nii.ac.jp/crid/1362544420395041024","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Asymmetric Synthesis of Tertiary Alcohols and α-Tertiary Amines via Cu-Catalyzed C−C Bond Formation to Ketones and Ketimines"}]},{"@id":"https://cir.nii.ac.jp/crid/1362825893277328256","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Catalytic asymmetric Henry reaction"}]},{"@id":"https://cir.nii.ac.jp/crid/1362825895578899712","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Constructing Quaternary Centers of Chirality: The Lanthanide Way to Trifluoromethyl-Substituted Tertiary Alcohols"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107369507345536","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Direct, Catalytic Enantioselective Nitroaldol (Henry) Reaction of Trifluoromethyl Ketones:  An Asymmetric Entry to α-Trifluoromethyl-Substituted Quaternary Carbons"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107371323851648","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Modern Alkyne Chemistry"}]},{"@id":"https://cir.nii.ac.jp/crid/1363388843336881408","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthesis of chiral tertiary trifluoromethyl alcohols by asymmetric nitroaldol reaction with a Cu(ii)-bisoxazolidine catalyst"}]},{"@id":"https://cir.nii.ac.jp/crid/1363388843703481216","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Fluorine in Pharmaceutical Industry: Fluorine-Containing Drugs Introduced to the Market in the Last Decade (2001–2011)"}]},{"@id":"https://cir.nii.ac.jp/crid/1363388843801237888","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Modern Fluoroorganic Chemistry"}]},{"@id":"https://cir.nii.ac.jp/crid/1363388845057872384","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Efficient Diastereoselective and Enantioselective Nitroaldol Reactions from Prochiral Starting Materials: Utilization of La-Li-6,6'-Disubstituted BINOL Complexes as Asymmetric Catalysts"}]},{"@id":"https://cir.nii.ac.jp/crid/1363388845898681856","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Catalytic Asymmetric Direct Henry Reaction of Ynals: Short Syntheses of (2<i>S</i>,3<i>R</i>)‐(+)‐Xestoaminol C and (−)‐Codonopsinines"}]},{"@id":"https://cir.nii.ac.jp/crid/1363670319376258688","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Applications of Fluorine in Medicinal Chemistry"}]},{"@id":"https://cir.nii.ac.jp/crid/1363670320654177920","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Brucine-Derived Amino Alcohol Catalyzed Asymmetric Henry Reaction: An Orthogonal Enantioselectivity Approach"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951794075808128","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Evaluation of 5‐<i>cis</i>‐Substituted Prolinamines as Ligands in Enantioselective, Copper‐Catalyzed Henry Reactions"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951795446966016","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Lanthanide (III) salt complexes: Arrayed acid‐base networks for enantioselective catalysis. The nitroaldol reaction upon aldehydes and trifluoromethylketones"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951795909360512","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A New Catalyst for the Asymmetric Henry Reaction: Synthesis of β-Nitroethanols in High Enantiomeric Excess"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951796184068864","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"New Highly Asymmetric Henry Reaction Catalyzed by Cu<sup>II</sup> and a <i>C</i><sub>1</sub>‐Symmetric Aminopyridine Ligand, and Its Application to the Synthesis of Miconazole"}]},{"@id":"https://cir.nii.ac.jp/crid/1364233269336397696","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Quaternary Stereocenters"}]},{"@id":"https://cir.nii.ac.jp/crid/1364233269900105728","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Enantioselective Henry Addition of Methyl 4-Nitrobutyrate to Aldehydes. Chiral Building Blocks for 2-Pyrrolidinones and Other Derivatives"}]},{"@id":"https://cir.nii.ac.jp/crid/1364233270131967232","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Ephedra in perspective – a current review"}]},{"@id":"https://cir.nii.ac.jp/crid/1364233270157739904","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Urea/Transition‐Metal Cooperative Catalyst for<i>anti</i>‐Selective Asymmetric Nitroaldol Reactions"}]},{"@id":"https://cir.nii.ac.jp/crid/1364233270407340032","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Enantioselective Henry (nitroaldol) reaction catalyzed by axially chiral guanidines"}]},{"@id":"https://cir.nii.ac.jp/crid/2051714791998240896","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Recent advances in catalytic asymmetric C-C bond-forming reactions to ketimines promoted by metal-based catalysts"}]}],"dataSourceIdentifier":[{"@type":"CROSSREF","@value":"10.1021/acs.orglett.7b03767"},{"@type":"KAKEN","@value":"PRODUCT-21618202"},{"@type":"KAKEN","@value":"PRODUCT-21767898"},{"@type":"CROSSREF","@value":"10.1246/bcsj.20200067_references_DOI_Vv6aGK0qeFEGhs9g9HbTKxYdiz"},{"@type":"CROSSREF","@value":"10.1002/ajoc.201800013_references_DOI_Vv6aGK0qeFEGhs9g9HbTKxYdiz"},{"@type":"CROSSREF","@value":"10.1002/asia.202101299_references_DOI_Vv6aGK0qeFEGhs9g9HbTKxYdiz"},{"@type":"CROSSREF","@value":"10.1021/jacs.8b08236_references_DOI_Vv6aGK0qeFEGhs9g9HbTKxYdiz"},{"@type":"CROSSREF","@value":"10.1016/j.tetlet.2023.154375_references_DOI_Vv6aGK0qeFEGhs9g9HbTKxYdiz"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.9b00982_references_DOI_Vv6aGK0qeFEGhs9g9HbTKxYdiz"}]}