Reactions of Hydroxyazolidines with π-Donor Heterocycles. 3. Reaction of 1-Acetyl-5-hydroxypyrazolidines with Oxindoles

Dlinnykh, I. V.; Golubeva, G. A.; Leshcheva, I. F.; Нестеров, В. В.; Antipin, M. Yu.; Свиридова, Л. А.

doi:10.1023/b:cohc.0000048286.22570.9f

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“…53 The use of potassium fluoride-modified alumina in benzene has been proved optimal for the all substrate pairs and the reactions were completed at 60 °C after 30-60 minutes. Application of catalyst 104 as an organocatalyst in this method follows the rules of green and sustainable chemistry.…”

Section: Scheme 33mentioning

confidence: 99%

Oxindole as starting material in organic synthesis

Ziarani¹,

Gholamzadeh²,

Lashgari³

et al. 2013

Arkivoc

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Section: Scheme 33mentioning

confidence: 99%

Oxindole as starting material in organic synthesis

Ziarani¹,

Gholamzadeh²,

Lashgari³

et al. 2013

Arkivoc

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Reactions of Hydroxyazolidines with π‐Donor Heterocycles. Part 3. Reaction of 1‐Acetyl‐5‐hydroxypyrazolidines with Oxindoles.

et al. 2005

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Pyrazole derivatives R 0180Reactions of Hydroxyazolidines with π-Donor Heterocycles. Part 3. Reaction of 1-Acetyl-5-hydroxypyrazolidines with Oxindoles. -Pyrazolidinyloxindoles (III) are prepared by the reaction of 5-hydroxypyrazolines (II) with 5-pyrazolones (I) on the surface of potassium fluoride-modified alumina as heterogeneous catalyst. -(DLINNYKH, I. V.; GOLUBEVA, G. A.; LESHCHEVA, I. F.; NESTEROV, V. V.; ANTIPIN, M. Y.; SVIRIDOVA, L. A.; Chem. Heterocycl. Compd. (N. Y.) 40 (2004) 9, 1142-1149; Lomonosov Moscow State Univ., Moscow 119899, Russia; Eng.) -R. Langenstrassen 23-116

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