Journal
CHEMISTRY LETTERS
Volume 44, Issue 7, Pages 902-904Publisher
CHEMICAL SOC JAPAN
DOI: 10.1246/cl.150239
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Funding
- Monbusho (The Ministry of Education, Culture, Sports, Science and Technology)
- Japan Science and Technology Agency
- Grants-in-Aid for Scientific Research [15H02177] Funding Source: KAKEN
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The reaction of aromatic amides containing a 5-chloro-8-aminoquinoline moiety as the directing group with arylsulfonyl chlorides in the presence of Ni(OTf)(2) as the catalyst results in sulfonylation at the ortho-position. Various arylsulfonyl chlorides can be used as the coupling partners.
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