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DDQ-promoted mild and efficient metal-free oxidative α-cyanation of N-acyl/sulfonyl 1,2,3,4-tetrahydroisoquinolinesoa mark
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Publication Year
2018-12-06
Publisher
MDPI AG
Citation
Molecules, Vol.23
Keyword
C(sp3)-H activationOxidationTetrahydroisoquinolineα-cyanation
Mesh Keyword
CatalysisCyanatesOxidation-ReductionOxidative StressTetrahydroisoquinolines
All Science Classification Codes (ASJC)
Analytical ChemistryChemistry (miscellaneous)Molecular MedicinePharmaceutical ScienceDrug DiscoveryPhysical and Theoretical ChemistryOrganic Chemistry
Abstract
A mild and highly efficient metal-free oxidative α-cyanation of N-acyl/sulfonyl 1,2,3,4-tetrahydroisoquinolines (THIQs) has been accomplished at an ambient temperature via DDQ oxidation and subsequent trapping of N-acyl/sulfonyl iminium ions with (n-Bu)3SnCN. Employing readily removable N-acyl/sulfonyl groups as protecting groups rather than N-aryl ones enables a wide range of applications in natural product synthesis. The synthetic utility of the method was illustrated using a short and efficient formal total synthesis of (±)-calycotomine in three steps.
ISSN
1420-3049
Language
eng
URI
https://dspace.ajou.ac.kr/dev/handle/2018.oak/30496
DOI
https://doi.org/10.3390/molecules23123223
Fulltext

Type
Article
Funding
Funding: This research was supported by the Basic Science Research Program through the National Research Fund of Korea (NRF) funded by Ministry of Science and ICT and the Ministry of Education (NRF-2017R1D1A1B03034612, NRF-2016R1A2B1012930, and NRF-2018R1D1A1A02086359) and Ajou University (No. S-2015-G0001-00345).
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Kim, Hong Pyo김홍표
Division of Pharmacy Sciences
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