The Reactions of Monoalkylthio- or Monoarylthio-Substituted Cyclopropenium Salt with Nitrogen Nucleophiles: Formation of Polyfunctionally Substituted Pyrroles or Pyrazoles

DOI: 10.1246/bcsj.65.698

Source and publish data:

Bulletin of the Chemical Society of Japan p. 698 - 702 (1992)

Update date:2022-08-03

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Authors:

Yoshida, Hiroshi

Utsumi, Fumitaka

Suzuki, Hideki

Ito, Satoru

Sakashita, Shin-ichi

et al et al

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Article abstract of DOI:10.1246/bcsj.65.698

The reactions of monoalkylthio- or monoarylthio-substituted cyclopropenium salt (1) with a number of secondary amines were studied.The amines, such as N-methylaniline, yielded indenes, whereas N-alkyl- or N-arylbenzylamines gave 1-alkyl or 1-aryl-2-phenyl

Full text of DOI:10.1246/bcsj.65.698

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