{"data":{"id":"10.6084/m9.figshare.1284142.v1","type":"dois","attributes":{"doi":"10.6084/m9.figshare.1284142.v1","prefix":"10.6084","suffix":"m9.figshare.1284142.v1","identifiers":[],"alternateIdentifiers":[],"creators":[{"name":"Sumran, Garima","nameType":"Personal","givenName":"Garima","familyName":"Sumran","affiliation":[],"nameIdentifiers":[]},{"name":"Aggarwal, Ranjana","nameType":"Personal","givenName":"Ranjana","familyName":"Aggarwal","affiliation":[],"nameIdentifiers":[]}],"titles":[{"title":"A convenient [hydroxy(tosyloxy)iodo]benzene-mediated one-pot synthesis of 2-arylimidazo[2,1-\u003ci\u003eb\u003c/i\u003e]benzothiazoles"}],"publisher":"Taylor \u0026 Francis","container":{},"publicationYear":2015,"subjects":[{"subject":"Hematology"},{"subject":"Science Policy"},{"subject":"Biological Sciences"},{"subject":"Immunology"},{"subject":"FOS: Clinical medicine","schemeUri":"http://www.oecd.org/science/inno/38235147.pdf","subjectScheme":"Fields of Science and Technology (FOS)"},{"subject":"FOS: Clinical medicine","subjectScheme":"Fields of Science and Technology (FOS)"},{"subject":"Ecology"},{"subject":"FOS: Biological sciences","schemeUri":"http://www.oecd.org/science/inno/38235147.pdf","subjectScheme":"Fields of Science and Technology (FOS)"},{"subject":"FOS: Biological sciences","subjectScheme":"Fields of Science and Technology (FOS)"},{"subject":"Chemistry"},{"subject":"Evolutionary Biology"},{"subject":"Biotechnology"},{"subject":"Molecular Biology"},{"subject":"Microbiology"},{"subject":"Biochemistry"},{"subject":"Biophysics"}],"contributors":[],"dates":[{"date":"2015-02-19","dateType":"Created"},{"date":"2016-01-19","dateType":"Updated"},{"date":"2015","dateType":"Issued"}],"language":null,"types":{"ris":"DATA","bibtex":"misc","citeproc":"dataset","schemaOrg":"Dataset","resourceType":"Dataset","resourceTypeGeneral":"Dataset"},"relatedIdentifiers":[{"relationType":"IsSupplementTo","relatedIdentifier":"10.1080/17415993.2014.996221","relatedIdentifierType":"DOI"},{"relationType":"IsPreviousVersionOf","relatedIdentifier":"10.6084/m9.figshare.1284142","relatedIdentifierType":"DOI"}],"relatedItems":[],"sizes":["1427028 Bytes"],"formats":[],"version":null,"rightsList":[{"rights":"Creative Commons Attribution 4.0 International","rightsUri":"https://creativecommons.org/licenses/by/4.0/legalcode","schemeUri":"https://spdx.org/licenses/","rightsIdentifier":"cc-by-4.0","rightsIdentifierScheme":"SPDX"}],"descriptions":[{"description":"Several 2-arylimidazo[2,1-\u003ci\u003eb\u003c/i\u003e]benzothiazoles (\u003cb\u003e4\u003c/b\u003e) have been conveniently synthesized in one-pot reactions \u003ci\u003evia\u003c/i\u003e α-tosyloxylation of enolizable ketones (\u003cb\u003e1\u003c/b\u003e) using [hydroxy(tosyloxy)iodo]benzene \u003cb\u003e2\u003c/b\u003e in acetonitrile, followed by treatment with 2-amino-6-(substituted)benzothiazoles (\u003cb\u003e3\u003c/b\u003e). The present protocol offers several advantages towards general access of 2-arylimidazo[2,1-\u003ci\u003eb\u003c/i\u003e]benzothiazoles, including an intriguing alternative to the literature protocols, a readily available nontoxic reagent, operational simplicity and an environmentally benign 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