REARRANGEMENT OF HUMULENE-8,9-EPOXIDE

被引：8

作者：

BRYSON, I ^{[1
]}

ROBERTS, JS ^{[1
]}

SATTAR, A ^{[1
]}

机构：

[1] UNIV STIRLING,DEPT CHEM,STIRLING FK9 4LA,SCOTLAND

来源：

TETRAHEDRON LETTERS | 1980年 / 21卷 / 02期

关键词：

D O I：

10.1016/S0040-4039(00)71413-4

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：201 / 204

页数：4

共 14 条

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[3]

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DEV, S .

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DEV, S .

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DAUBEN, WG ;

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VIETMEYER, ND .

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[7] STUDIES IN SESQUITERPENES .46. SESQUITERPENES FROM OLEORESIN OF DIPTEROCARPUS-PILOSUS - HUMULENE EPOXIDE-III, CARYOPHYLLENOL-I AND CARYOPHYLLENOL-II [J].

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DEV, S .

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[8]

McKervey M. A., 1970, CHEM COMMUN, V117

[9]

MLOTKIEWICZ JA, 1979, TETRAHEDRON LETT, P3887

[10] 5,9-DIHYDROXY-4,8,11,11-TETRAMETHYLTRICYCLO[6.3.0.02,4]UNDECANE - ACID-CATALYZED CYCLIZATION PRODUCT OF 6,7-EPOXYHUMULA-2,9-DIENE [J].

NAMIKAWA, M ;

MURAE, T ;

TAKAHASHI, T .

BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1978, 51 (12) :3616-3621

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