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Direct and Efficient C(sp3)–H Functionalization of N-Acyl/Sulfonyl Tetrahydroisoquinolines (THIQs) With Electron-Rich Nucleophiles via 2,3-Dichloro-5,6-Dicyano-1,4-Benzoquinone (DDQ) Oxidationoa mark
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dc.contributor.authorYu, Heesun-
dc.contributor.authorKim, Hyoungsu-
dc.contributor.authorBaek, Seung Hoon-
dc.contributor.authorLee, Dongjoo-
dc.date.issued2020-07-29-
dc.identifier.issn2296-2646-
dc.identifier.urihttps://dspace.ajou.ac.kr/dev/handle/2018.oak/31470-
dc.description.abstractA highly efficient metal-free oxidative direct C(sp3)–H functionalization of N-acyl/sulfonyl 1,2,3,4-tetrahydroisoquinolines (THIQs) with a wide range of electron-rich nucleophiles was accomplished under mild conditions through oxidation with DDQ and subsequent trapping of the resulting reactive and stable N-acyl/sulfonyl iminium ions. The synthetic utility of this method was illustrated by a concise and efficient total synthesis of (±)-benzo[a]quinolizidine (10) in 3 steps from the known N-Cbz 1,2,3,4-THIQ 4b.-
dc.description.sponsorshipWe gratefully acknowledge financial support of this work by the Basic Science Research Program through the National Research Fund of Korea (NRF) funded by the Ministry of Science and ICT and the Ministry of Education (NRF-2016R1A2B1012930 and NRF-2018R1D1A1A02086359).-
dc.language.isoeng-
dc.publisherFrontiers Media S.A.-
dc.titleDirect and Efficient C(sp3)–H Functionalization of N-Acyl/Sulfonyl Tetrahydroisoquinolines (THIQs) With Electron-Rich Nucleophiles via 2,3-Dichloro-5,6-Dicyano-1,4-Benzoquinone (DDQ) Oxidation-
dc.typeArticle-
dc.citation.titleFrontiers in Chemistry-
dc.citation.volume8-
dc.identifier.bibliographicCitationFrontiers in Chemistry, Vol.8-
dc.identifier.doi10.3389/fchem.2020.00629-
dc.identifier.scopusid2-s2.0-85089413347-
dc.identifier.urlhttp://journal.frontiersin.org/journal/chemistry-
dc.subject.keywordDDQ-
dc.subject.keywordelectron-rich-
dc.subject.keywordnatural products-
dc.subject.keywordoxidation-
dc.subject.keywordtetrahydroisoquinoline-
dc.description.isoatrue-
dc.subject.subareaChemistry (all)-
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