A Convenient Synthesis of N-Vinylpyridinium Perchlorate and a Study of N-Vinylpyridinium Cations as Michael Reaction Acceptors

DOI: 10.1021/jo00170a028

Source and publish data:

Journal of Organic Chemistry p. 4017 - 4021 (1983)

Update date:2022-08-03

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Authors:

Katritzky, Alan R.

Rubio, Olga

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Article abstract of DOI:10.1021/jo00170a028

The titel compound is easily prepared from 1-(2-bromoethyl)pyridinium bromide and sodium hydroxide. 1-Vinylpyridinium and 1-vinyl-2,4,6-triphenylpyridinium cations add N, S, and C nucleophiles in Michael-type reactions.

Full text of DOI:10.1021/jo00170a028

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Product name:1-(2-piperidinoethyl)-2,4,6-triphenylpyridinium tetrafluoroborate

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