4.0 Article

Five-membered 2,3-dioxo heterocycles:: LIII.: Reaction of 3-Aroyl-1H-pyrrolo[2,1-c][1,4]benzoxazine-1,2,4-triones with substituted 1,3,3-trimethyl-3,4-dihydroisoquinolines.: A new approach to 13-aza analogs of steroids

期刊

RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
卷 43, 期 9, 页码 1330-1333

出版社

MAIK NAUKA/INTERPERIODICA/SPRINGER
DOI: 10.1134/S1070428007090114

关键词

-

向作者/读者索取更多资源

3-Aroyl-1H-pyrrolo[2,1-c][1,4]benzoxazine-1,2,4-triones reacted with substituted 1,3,3-trimethyl-3,4-dihydroisoquinolines to give the corresponding 3-aroyl-4-hydroxy-1-(2-hydroxyphenyl)-5',5'-dimethyl-5',6'-dihydro-1H-spiro[pyrrole-2,2'-pyrrolo[2, 1-a]isoquinoline]-3',5-diones. 7',8'-Benzo derivatives of the latter may be regarded as 13-azagonane analogs having a spiro-fused pyrrole ring at C-16.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.0
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据