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onesobtainedfromthisprocessenabledtheefficientconstruction
of an indoloisoquinolinone framework through reorganization of
the molecular skeleton. Considering the valuable structure of the
products, the protocol described herein could be beneficial to N-
heterocyclic chemistry as well as total syntheses of alkaloids.
̀
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ASSOCIATED CONTENT
* Supporting Information
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Full experimental details and characterization data (PDF)
Accession Codes
CCDC 1865715 contains the supplementary crystallographic
data for this paper. These data can be obtained free of charge via
Crystallographic Data Centre, 12 Union Road, Cambridge CB2
1EZ, UK; fax: +44 1223 336033.
AUTHOR INFORMATION
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Corresponding Author
ORCID
Notes
The authors declare no competing financial interest.
ACKNOWLEDGMENTS
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This paper is dedicated to Professor Yong Hae Kim on the
occasion of his 80th birthday. This work was supported by both
the Basic Science Research Program and Nano·Material
Technology Department Program through the National
Research Foundation of Korea (NRF) funded by the Korea
government(MSIP)(Nos. 2012M3A7B4049644, 2014-011165,
2015R1A2A2A01002559, and 2018R1A2A2A05018392). We
thank Dr. Ji-Eun Lee (Central Instrument Facility, Gyeongsang
National University) for X-ray crystallographic analysis.
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