ChemInform Abstract: Acetylenic Chemistry. Part 10. Cycloisomerization of 3‐Acetyl‐3‐(prop‐2‐ynyl)indol‐2‐one to 3‐Acetyl‐2‐methyl‐2H‐furo(2,3‐b)indole.

Reisch, J.; Labitzke, H.; Bathe, A.

doi:10.1002/chin.198835163

ChemInform

1988

DOI: 10.1002/chin.198835163

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ChemInform Abstract: Acetylenic Chemistry. Part 10. Cycloisomerization of 3‐Acetyl‐3‐(prop‐2‐ynyl)indol‐2‐one to 3‐Acetyl‐2‐methyl‐2H‐furo(2,3‐b)indole.

J. Reisch¹,

H. Labitzke²,

A. Bathe³

Abstract: ChemInform Abstract The propynylindolinone (I) reacts with PPA and water to form the propanone (II). The acetylated analogue (III) is cyclized upon acidic treatment to give the furoindole (IV).

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ChemInform Abstract: Acetylenic Chemistry. Part 10. Cycloisomerization of 3‐Acetyl‐3‐(prop‐2‐ynyl)indol‐2‐one to 3‐Acetyl‐2‐methyl‐2H‐furo(2,3‐b)indole.

Abstract: ChemInform Abstract The propynylindolinone (I) reacts with PPA and water to form the propanone (II). The acetylated analogue (III) is cyclized upon acidic treatment to give the furoindole (IV).

Cited by 0 publications

References 1 publication

No citations

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