Journal
ORGANIC LETTERS
Volume 10, Issue 6, Pages 1163-1166Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol800049b
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Funding
- National Research Foundation of Korea [R01-2007-000-10618-0, R11-1999-056-03007-0, 과06A1506] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
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It is revealed that 2-sulfonyliminoindolines can be efficiently synthesized by the Cu-catalyzed cyclization reaction of N-alkyl- or aryl-substituted 2-ethynylanilines with sulfonyl azides. This new route to the indoline derivatives is characterized by mild reaction conditions, facile introduction of functional groups at the 2-poiltion of the indoline ring, and the wide substrate scope. Selective transformation of indoline to oxindole and isatin analogs is also demonstrated.
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