Regioselective condensations and N-acylations of 3-aminorhodanines

DOI: 10.1002/ardp.19933261109

Source and publish data:

Archiv der Pharmazie p. 887 - 891 (1993)

Update date:2022-07-29

Topics:

Authors:

Hanefeld

Schlitzer

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Article abstract of DOI:10.1002/ardp.19933261109

3-Aminorhodanines were condensed regioselectively with aldehydes at the 3-amino or 5-methylene group. The 3-amino function was acylated with acid chlorides or anhydrides.

Full text of DOI:10.1002/ardp.19933261109

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