NITROSATIONS OF HYDRAZINE DERIVATIVES .10 . OXIDATIONS OF CARBAMOTHIOATES .11. REACTIONS OF 3-AMINORHODANINES UNDER NITROSATING CONDITIONS

Citation
W. Hanefeld et al., NITROSATIONS OF HYDRAZINE DERIVATIVES .10 . OXIDATIONS OF CARBAMOTHIOATES .11. REACTIONS OF 3-AMINORHODANINES UNDER NITROSATING CONDITIONS, Archiv der pharmazie, 326(11), 1993, pp. 871-874
Citations number
14
Categorie Soggetti
Chemistry,"Pharmacology & Pharmacy
Journal title
ISSN journal
03656233
Volume
326
Issue
11
Year of publication
1993
Pages
871 - 874
Database
ISI
SICI code
0365-6233(1993)326:11<871:NOHD..>2.0.ZU;2-4
Abstract
C-5-unsubstituted 5-aminorhodanines 1 are converted to 5-hydroximino-r hodanines 2 with NaNO2/HCl, nitrosyl- and nitronium-tetrafluoroborate. With HNO3, 5-hydroximinothiazolidine-2,4-diones 3 arise. Under drasti c conditions 5-arallcyliden-3-aminorhodanines 7 are desulfurized oxida tively in 2-position by HNO2.