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

被引：4

作者：

HANEFELD, W

HELFRICH, V

HUNZ, I

JALILI, MA

SCHLITZER, M

机构：

[1] Institut für Pharmazeutische Chemie der Philipps-Universität Marburg, Marburg, D-35037

来源：

ARCHIV DER PHARMAZIE | 1993年 / 326卷 / 11期

关键词：

D O I：

10.1002/ardp.19933261106

中图分类号：

R914 [药物化学];

学科分类号：

100701 ;

摘要：

C-5-unsubstituted 5-aminorhodanines 1 are converted to 5-hydroximino-rhodanines 2 with NaNO2/HCl, nitrosyl- and nitronium-tetrafluoroborate. With HNO3, 5-hydroximinothiazolidine-2,4-diones 3 arise. Under drastic conditions 5-arallcyliden-3-aminorhodanines 7 are desulfurized oxidatively in 2-position by HNO2.

引用

页码：871 / 874

页数：4

共 7 条

[1] NITROSATIONS OF HYDRAZINE DERIVATIVES .11. 5-NITRORHADANINES FROM 5-MONOSUBSTITUTED RHODANINE DERIVATIVES UNDER NITROSATING CONDITIONS
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ARCHIV DER PHARMAZIE, 1993, 326 (11) : 875 - 878
[2] NITROSATING ON HYDRAZINE DERIVATIVES .7. REACTIONS OF PHENELZIN, ENDRALAZIN, AND PROCARBAZIN UNDER NITROSATING CONDITIONS
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[3] NITROSATIONS WITH HYDRAZINE DERIVATIVES .6. NOVEL REACTION OF ORAL ANTIDIABETICS OF THE SULFONYLSEMICARBAZIDE TYPE UNDER NITROSATING CONDITIONS
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HARTMANN, M
ARCHIV DER PHARMAZIE, 1993, 326 (12) : 925 - 927
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