{"@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/1361137045848150528.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1021/cr900382t"}},{"identifier":{"@type":"URI","@value":"https://pubs.acs.org/doi/pdf/10.1021/cr900382t"}}],"dc:title":[{"@value":"Synthesis and Applications of <i>tert</i>-Butanesulfinamide"}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1381137045848150529","@type":"Researcher","foaf:name":[{"@value":"MaryAnn T. Robak"}],"jpcoar:affiliationName":[{"@value":"Department of Chemistry, University of California, Berkeley, California 94720"}]},{"@id":"https://cir.nii.ac.jp/crid/1381137045848150528","@type":"Researcher","foaf:name":[{"@value":"Melissa A. Herbage"}],"jpcoar:affiliationName":[{"@value":"Department of Chemistry, University of California, Berkeley, California 94720"}]},{"@id":"https://cir.nii.ac.jp/crid/1381137045848150530","@type":"Researcher","foaf:name":[{"@value":"Jonathan A. Ellman"}],"jpcoar:affiliationName":[{"@value":"Department of Chemistry, University of California, Berkeley, California 94720"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"00092665"},{"@type":"EISSN","@value":"15206890"}],"prism:publicationName":[{"@value":"Chemical Reviews"}],"dc:publisher":[{"@value":"American Chemical Society (ACS)"}],"prism:publicationDate":"2010-04-26","prism:volume":"110","prism:number":"6","prism:startingPage":"3600","prism:endingPage":"3740"},"reviewed":"false","url":[{"@id":"https://pubs.acs.org/doi/pdf/10.1021/cr900382t"}],"createdAt":"2010-04-26","modifiedAt":"2023-04-08","relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1360002214401134720","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"(Pentamethylcyclopentadienyl)cobalt(III)‐Catalyzed C–H Bond Functionalization: From Discovery to Unique Reactivity and Selectivity"}]},{"@id":"https://cir.nii.ac.jp/crid/1360002216612899200","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Pd-Catalyzed Selective Synthesis of Cyclic Sulfonamides and Sulfinamides Using K<sub>2</sub>S<sub>2</sub>O<sub>5</sub> as a Sulfur Dioxide Surrogate"}]},{"@id":"https://cir.nii.ac.jp/crid/1360002216903259776","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Dearylation of arylphosphine oxides using a sodium hydride–iodide composite"}]},{"@id":"https://cir.nii.ac.jp/crid/1360004229994476416","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Highly Conformationally Restricted Cyclopropane Tethers with Three‐Dimensional Structural Diversity Drastically Enhance the Cell Permeability of Cyclic Peptides"}]},{"@id":"https://cir.nii.ac.jp/crid/1360004229994549120","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Cyclopropane‐Based Peptidomimetics Mimicking Wide‐Ranging Secondary Structures of Peptides: Conformational Analysis and Their Use in Rational Ligand Optimization"}]},{"@id":"https://cir.nii.ac.jp/crid/1360004232525473920","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Stereoselective synthesis of Xaa-Yaa type (Z)-chloroalkene dipeptide isosteres via efficient utilization of organocopper reagents mediated allylic alkylation"}]},{"@id":"https://cir.nii.ac.jp/crid/1360004232527100672","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Achiral β-amino alcohols as efficient ligands for the ruthenium-catalysed asymmetric transfer hydrogenation of sulfinylimines"}]},{"@id":"https://cir.nii.ac.jp/crid/1360004233141721216","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Remote Stereoinduction in the Organocuprate-Mediated Allylic Alkylation of Allylic <i>gem</i>-Dichlorides: Highly Diastereoselective Synthesis of (<i>Z</i>)-Chloroalkene Dipeptide Isosteres"}]},{"@id":"https://cir.nii.ac.jp/crid/1360004233151235840","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis of a Chloroalkene Dipeptide Isostere-Containing Peptidomimetic and Its Biological Application"}]},{"@id":"https://cir.nii.ac.jp/crid/1360004233249398144","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Concise Synthesis of α-Trisubstituted Amines from Ketones Using <i>N</i>-Methoxyamines"}]},{"@id":"https://cir.nii.ac.jp/crid/1360004233249550464","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Three-Dimensional Structural Diversity-Oriented Peptidomimetics Based on the Cyclopropylic Strain"}]},{"@id":"https://cir.nii.ac.jp/crid/1360005518093601408","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"CO<sub>2</sub> Activation by Lewis Pairs Generated Under Copper Catalysis Enables Difunctionalization of Imines"}]},{"@id":"https://cir.nii.ac.jp/crid/1360017282463062400","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Regioselective anti-Silyllithiation of Propargylic Amines"}]},{"@id":"https://cir.nii.ac.jp/crid/1360306904403510528","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Design and Synthesis of a C\n               2-Symmetric Cyclic Decapeptide and Its Peptidomimetic as Potential Inhibitors against Amyloid-β Aggregation"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567179878785536","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Asymmetric Synthesis of Less Accessible α‐Tertiary Amines from Alkynyl <i>Z‐</i>Ketimines"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567183084487040","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Stereoselective Synthesis of Nitrogen-Containing Compounds from Enamines"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567183899251328","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Enantioselective Synthesis of Arylglycine Derivatives by Asymmetric Addition of Arylboronic Acids to Imines"}]},{"@id":"https://cir.nii.ac.jp/crid/1360568464449263616","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Asymmetric Synthesis of Chiral Sulfoximines through the S‐Alkylation of Sulfinamides"}]},{"@id":"https://cir.nii.ac.jp/crid/1360576118704095872","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Practical Asymmetric Synthesis of Chiral Sulfoximines via Sulfur-Selective Alkylation"}]},{"@id":"https://cir.nii.ac.jp/crid/1360580232396936320","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Solid-Phase-Based Synthesis of Lactazole-Like Thiopeptides"}]},{"@id":"https://cir.nii.ac.jp/crid/1360588380600952704","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Diastereoselective synthesis of (\n                    <i>Z</i>\n                    )-fluoroalkene dipeptide isosteres utilizing chiral auxiliaries"}]},{"@id":"https://cir.nii.ac.jp/crid/1360848657457704064","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Diastereoselective synthesis of 1,3-diamines by a domino reaction of imines, enamines, and trichlorosilane"}]},{"@id":"https://cir.nii.ac.jp/crid/1360861707356771072","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Formal Synthesis of Ecteinascidin 743 via an Intramolecular Cascade Heck Reaction to Construct the Diazabicyclo[3.3.1]nonane Framework"}]},{"@id":"https://cir.nii.ac.jp/crid/1360865815509230080","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Transsulfinamidation of Sulfinamides with Amines"}]},{"@id":"https://cir.nii.ac.jp/crid/1360865815510463872","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Practical Asymmetric Synthesis of Sulfoximines and Sulfimides from Sulfinamides"}]},{"@id":"https://cir.nii.ac.jp/crid/1360869855119879936","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Design, synthesis and evaluation of bioactivity of peptidomimetics based on chloroalkene dipeptide isosteres"}]},{"@id":"https://cir.nii.ac.jp/crid/1361131418000436992","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Asymmetric Synthesis of Chiral Sulfoximines via the <i>S</i>-Arylation of Sulfinamides"}]},{"@id":"https://cir.nii.ac.jp/crid/1390564238105443072","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Development for Peptidomimetic Chemistry Utilizing the Oxetanyl Structure"},{"@language":"ja","@value":"オキセタニル骨格を活用したペプチドミメティック化学への展開"}]}],"dataSourceIdentifier":[{"@type":"CROSSREF","@value":"10.1021/cr900382t"},{"@type":"CROSSREF","@value":"10.1002/adsc.201700042_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"},{"@type":"CROSSREF","@value":"10.1039/c8cc00289d_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"},{"@type":"CROSSREF","@value":"10.1002/chem.201604946_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"},{"@type":"CROSSREF","@value":"10.1002/chem.201605312_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"},{"@type":"CROSSREF","@value":"10.1055/a-2047-8456_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"},{"@type":"CROSSREF","@value":"10.1021/ol300622r_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.5b00611_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"},{"@type":"CROSSREF","@value":"10.1016/j.tet.2017.06.003_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"},{"@type":"CROSSREF","@value":"10.1055/a-2536-8969_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"},{"@type":"CROSSREF","@value":"10.1071/ch11225_references_DOI_AbVUDKtb26gKVepbUFaE1vVLRjw"},{"@type":"CROSSREF","@value":"10.1002/anie.201710084_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"},{"@type":"CROSSREF","@value":"10.1002/anie.201911021_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"},{"@type":"CROSSREF","@value":"10.1016/j.tetlet.2010.12.031_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"},{"@type":"CROSSREF","@value":"10.1021/ol400469w_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"},{"@type":"CROSSREF","@value":"10.1021/acs.joc.7b01923_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"},{"@type":"CROSSREF","@value":"10.1021/acs.joc.1c02424_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.2c02870_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"},{"@type":"CROSSREF","@value":"10.1039/d5ob00189g_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"},{"@type":"CROSSREF","@value":"10.1021/acsmedchemlett.7b00234_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"},{"@type":"CROSSREF","@value":"10.5059/yukigoseikyokaishi.77.720_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.2c03357_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.3c02534_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"},{"@type":"CROSSREF","@value":"10.1055/a-2127-1260_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"},{"@type":"CROSSREF","@value":"10.1016/j.bmc.2024.117811_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"},{"@type":"CROSSREF","@value":"10.1016/j.tetlet.2014.01.152_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.7b00402_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"},{"@type":"CROSSREF","@value":"10.1021/jacs.9b11423_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"},{"@type":"CROSSREF","@value":"10.1021/jacs.9b11298_references_DOI_1ZMdjG92qu4i7jucOuIIbXwv5gU"}]}