Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/4829
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dc.contributor.authorDalal, Arup-
dc.contributor.authorBabu, Srinivasarao Arulananda-
dc.date.accessioned2023-08-18T09:59:46Z-
dc.date.available2023-08-18T09:59:46Z-
dc.date.issued2021-
dc.identifier.citationSynthesis, 53(18), 3307–3324.en_US
dc.identifier.urihttps://www.thieme-connect.de/products/ejournals/abstract/10.1055/a-1472-0881-
dc.identifier.urihttp://hdl.handle.net/123456789/4829-
dc.descriptionOnly IISERM authors are available in the recorden_US
dc.description.abstractWe report the application of the Pd(II)-catalyzed, directing-group-aided C–H arylation/alkylation tactics to functionalize the pyrene core, especially, the relatively inaccessible C2 and K-region C10 positions of the pyrene core and augmentation of the library of pyrene derivatives with C1,C2- and C1,C10-disubstituted pyrene motifs. The Pd(II)-catalyzed β-C–H arylation/alkylation of the C2-position of pyrene-1-carboxamide possessing an 8-aminoquinoline directing group yielded various C1,C2-disubstituted pyrenes. Similarly, the Pd(II)-catalyzed selective γ-C–H arylation/alkylation of the C10-position of N-(pyren-1-yl)picolinamide, possessing a picolinamide directing group, yielded various C1,C10-disubstituted pyrenes. Examples of C(9)–H arylation of pyrene-1-carboxamide and the removal of the directing group after the C–H arylation/alkylation reactions were also shown. The structures of representative pyrene derivatives were confirmed by the X-ray structure analysis. Given the importance of the pyrene derivatives in various fields of chemical sciences, this report is a contribution towards augmentation of the library of pyrene derivatives with C1,C2- and C1,C10-disubstituted pyrene amide motifs.en_US
dc.language.isoen_USen_US
dc.publisherThiemeen_US
dc.subjectpalladium - pyreneen_US
dc.subjectC–H arylation/alkylationen_US
dc.titlePd(II)-Catalyzed Directing-Group-Aided C–H Arylation and Alkylation of Pyrene Core: Synthesis of C1,C2- and C1,C10-Disubstituted Pyrene Motifsen_US
dc.typeArticleen_US
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