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dc.contributor.authorFukuyama, Takahideen_US
dc.contributor.authorNishikawa, Tomohiroen_US
dc.contributor.authorYamada, Keiichien_US
dc.contributor.authorRavelli, Davideen_US
dc.contributor.authorFagnoni, Maurizioen_US
dc.contributor.authorRyu, Ilhyongen_US
dc.date.accessioned2018-08-21T05:53:02Z-
dc.date.available2018-08-21T05:53:02Z-
dc.date.issued2017-12-01en_US
dc.identifier.issn1523-7060en_US
dc.identifier.urihttp://dx.doi.org/10.1021/acs.orglett.7b03339en_US
dc.identifier.urihttp://hdl.handle.net/11536/144190-
dc.description.abstractTetrabutylammonium decatungstate (TBADT)-photocatalyzed C-H functionalization of alkylpyridines was investigated. Unlike alkylbenzene counterparts, alkylation of alpha-C-H bonds did not proceed for the reaction of 2- and 4-alkylpyridines and reluctantly proceeded for 3-alkylpyridines, which allow site-selective C(sp(3))-H functionalization at nonbenzylic positions. The observed nonbenzylic site selectivities are rationalized by the polar inductive effects of pyridyl groups in the S-H(2) transition states. Consecutive gamma-functionalization and alpha-bromofunctionalization were successfully carried out in selected cases.en_US
dc.language.isoen_USen_US
dc.titlePhotocatalyzed Site-Selective C(sp(3))-H Functionalization of Alkylpyridines at Non-Benzylic Positionsen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/acs.orglett.7b03339en_US
dc.identifier.journalORGANIC LETTERSen_US
dc.citation.volume19en_US
dc.citation.spage6436en_US
dc.citation.epage6439en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000417229000044en_US
Appears in Collections:Articles