PHOTOCYCLIZATION OF ENAMIDES .13. SUBSTITUENT EFFECTS IN THE PHOTOCYCLIZATION OF N-BENZOYLENAMINES

被引：19

作者：

NINOMIYA, I

KIGUCHI, T

YAMAMOTO, O

NAITO, T

机构：

[1] Kobe Women's College of Pharmacy, Motoyamakita, Higashinada

来源：

JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | 1979年 / 07期

关键词：

D O I：

10.1039/p19790001723

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

trans-Hexahydrophenanthridones (IIa-g) and trans-tetrahydrobenzo[c] phenanthridones (VIa-e) were prepared by stereospecific photocyclisation of a variety of N-benzoylenamines (Ia-n) and (Va-g) bearing either electron-donating or -attracting substituents on the benzoyl group. Suprafacial [1,5] migration of an o-methoxy-group upon cyclisation and photoinduced trans-cis-isomerisation of some benzo[c]phenanthridones (VIa-c) were observed.

引用

页码：1723 / 1728

页数：6

共 14 条

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