Journal of the Chemical Society. Perkin transactions I p. 729 - 733 (1996)
Update date:2022-08-24
Topics:
Kawasaki, Tomomi
Masuda, Kouhei
Baba, Yasutaka
Terashima, Romi
Takada, Kana
Sakamoto, Masanori
Treatment of 2,3-dihydro-1H-indol-3-ones with allyl alcohols in the presence of camphorsulfonic acid and magnesium sulfate at 130°C gave, via condensation and a Claisen rearrangement, 2-allyl-2,3-dihydro-1H-indol-3-ones in good yields. The stereochemistry of the products was determined by NOE experiments.
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