OZONOLYSIS OF 5-BROMO-2-PHENYLOXAZOLE AND 5-ETHOXY-2-PHENYLOXAZOLE - THE PRODUCTS AND THE REACTION-MECHANISM

被引：6

作者：

KASHIMA, C ^{[1
]}

ARAO, H ^{[1
]}

机构：

[1] UNIV TSUKUBA, DEPT CHEM, TSUKUBA, IBARAKI 305, JAPAN

来源：

JOURNAL OF HETEROCYCLIC CHEMISTRY | 1991年 / 28卷 / 03期

关键词：

D O I：

10.1002/jhet.5570280345

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The ozonolysis of 2-phenyloxazoles having the good leaving group as an anion at C-5 position gave mainly N-benzoylisocyanate (2) with the formation of carbon dioxide.

引用

页码：805 / 806

页数：2

共 8 条

[1]

KASHIMA C, 1989, SYNTHESIS-STUTTGART, P873

[2] CONVENIENT SYNTHESIS OF MIXED ANHYDRIDES BY THE OZONOLYSIS OF OXAZOLES [J].

KASHIMA, C ;

HIBI, S ;

HARADA, K ;

OMOTE, Y .

JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1988, (03) :529-533

[3] DEUTERIOFORMYLATION BY THE OZONOLYSIS OF 2-DEUTERIO-5-PHENYLOXAZOLES OR 5-DEUTERIO-2-PHENYLOXAZOLES [J].

KASHIMA, C ;

ARAO, H .

HETEROCYCLES, 1990, 31 (08) :1513-1516

[4] FORMYLATION REACTION USING THE OZONOLYSATE OF OXAZOLE [J].

KASHIMA, C ;

ARAO, H ;

HIBI, S ;

OMOTE, Y .

TETRAHEDRON LETTERS, 1989, 30 (12) :1561-1562

[5]

KASHIMA C, IN PRESS J CHEM RES

[6]

KASHIMA C, UNPUB

[7]

KONDRATEVA GY, 1962, ZH OBSHCH KHIM+, V32, P2348

[8]

Rubin M. B., 1964, J CHEM EDUC, V41, P388

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