ENZYMATIC-REACTION OF (3E,6S,7S)-LAUREDIOL AND THE MOLECULAR MODELING STUDIES ON THE CYCLIZATION OF LAUREDIOLS

被引：24

作者：

ISHIHARA, J ^{[1
]}

KANOH, N ^{[1
]}

MURAI, A ^{[1
]}

机构：

[1] HOKKAIDO UNIV,FAC SCI,DEPT CHEM,SAPPORO,HOKKAIDO 060,JAPAN

来源：

TETRAHEDRON LETTERS | 1995年 / 36卷 / 05期

关键词：

D O I：

10.1016/0040-4039(94)02329-A

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The biosynthetic reaction of (3E,6S,7S)-laurediol with H2O2 and NaBr by lactoperoxidase afforded (E)-prelaureation. The molecular modeling studies on the bromo-ether cyclization reactions of laurediols are also described.

引用

页码：737 / 740

页数：4

共 9 条

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[8] ISOMERIZATION OF THE (Z)-ENYNE UNIT TO THE (E)-ENYNE UNIT - CONVERSION OF LAUREATIN TO (E)-ISOLAUREATIN
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[9] CONVERSION OF 2-HEPTENOLIDES INTO SUBSTITUTED OXOCENE SYSTEMS - ITS APPLICATION TO THE SYNTHESIS OF (+)-LAUTHISAN
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