Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 76, Issue 4, Pages 1163-1166Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jo1021772
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Funding
- Ministry of Education, Culture, Sports, Science and Technology, Japan [19350095]
- Society of Iodine Science
- Japan Society for the Promotion of Science (JSPS)
- Grants-in-Aid for Scientific Research [19350095] Funding Source: KAKEN
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Upon photoirradiation of o-alkynylaryl isocyanides in the presence of iodine, the intramolecular cyclization of o-alkynylaryl isocyanides proceeds to afford the corresponding 2,4-diiodoquinolines in good yields. 2,4-Diiodoquinolines can be employed in transition metal-catalyzed cross-coupling reactions.
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