ABSOLUTE STEREOCHEMISTRY OF SALVIC ACID AND RELATED DITERPENES

被引：4

作者：

GONZALEZ, AG ^{[1
]}

PEREZ, EMR ^{[1
]}

DIAZ, JG ^{[1
]}

BARRERA, JB ^{[1
]}

机构：

[1] CSIC,CTR PROD NAT ORGAN ANTONIO GONZALEZ,CARRETERA ESPERANZA 2,E-38206 TENERIFE,SPAIN

来源：

JOURNAL OF NATURAL PRODUCTS | 1991年 / 54卷 / 02期

关键词：

D O I：

10.1021/np50074a045

中图分类号：

Q94 [植物学];

学科分类号：

071001 ;

摘要：

The stereochemistry of salvic acid [1] and related diterpenes has been established on the basis of their chemical transformation into methyl dihydroeperuate.

引用

页码：609 / 611

页数：3

共 5 条

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[2] LABDANE DITERPENES FROM CISTUS SYMPHYTIFOLIUS [J].

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CORTES, M ;

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HERNANDEZ, R ;

SUAREZ, E .

PHYTOCHEMISTRY, 1981, 20 (09) :2255-2258

[3] DITERPENES AND OTHER CONSTITUENTS OF EUPATORIUM-SALVIA [J].

GONZALEZ, AG ;

BARRERA, JB ;

DIAZ, JG ;

PEREZ, EMR ;

YANES, AC ;

RAUTER, P ;

POZO, J .

PHYTOCHEMISTRY, 1990, 29 (01) :321-323

[4]

HOENEISEN M, 1979, REV LAT AM ING QUIM, V10, P37

[5]

TERESA JD, 1985, PHYTOCHEMISTRY, V24, P791

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