ORTHO-DIENONE SYNTHESIS BY PHENOLIC OXIDATION OF DIHYDROXY-1-PHENETHYL-1,2,3,4-TETRAHYDROISOQUINOLINE

被引：9

作者：

KAMETANI, T

FUKUMOTO, K

HAYASAKA, T

SATOH, F

KIGASAWA, K

机构：

来源：

JOURNAL OF THE CHEMICAL SOCIETY C-ORGANIC | 1969年 / 01期

关键词：

D O I：

10.1039/j39690000004

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Oxidation of 1,2,3,4-tetrahydro-7-hydroxy-1-(2-hydroxy-4-methoxyphenethyl)-6-methoxy-2- methylisoquinoline (III) and its methoxy-analogue (IV) with ferric chloride gave ortho-dienone-type homoproaporphines [(Va) and (VIa), respectively]. The mass spectral patterns of the ortho-dienones [(Va) and (VIa)] are also discussed.

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