Biotransformation of the fungistatic sesquiterpenoid patchoulol by Botrytis cinerea

被引:55
作者
Aleu, J
Hanson, JR
Galán, RH
Collado, IG
机构
[1] Univ Cadiz, Fac Ciencias, Dept Quim Organ, Puerto Real 11510, Spain
[2] Univ Sussex, Sch Chem Phys & Environm Sci, Brighton BN1 9QJ, E Sussex, England
来源
JOURNAL OF NATURAL PRODUCTS | 1999年 / 62卷 / 03期
关键词
D O I
10.1021/np980416e
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Biotransformation of the fungistatic sesquiterpenoid patchoulol (1) by the fungus Botrytis cinerea affords the 5-, 7- and (8R)-hydroxy (2, 3, and 5) derivatives as the major metabolites, together with a number of minor metabolites (4, 6-9) arising from hydroxylation at C-2, C-3, C-5, C-9, C-13, and C-14.
引用
收藏
页码:437 / 440
页数:4
相关论文
共 8 条
[1]  
ARANTES SF, UNPUB
[2]  
COLEYSMITH JR, 1980, BIOL BOTRYTIS, P153
[3]   SYNTHESIS AND ANTIFUNGAL ACTIVITY OF ANALOGS OF NATURALLY-OCCURRING BOTRYDIAL PRECURSORS [J].
COLLADO, IG ;
ALEU, J ;
MACIASSANCHEZ, AJ ;
HERNANDEZGALAN, R .
JOURNAL OF CHEMICAL ECOLOGY, 1994, 20 (10) :2631-2644
[4]  
COLLADO IG, 1994, J NAT PRODUCTS, V59, P738
[5]   NATURAL ABUNDANCE C-13-C-13 COUPLING-CONSTANTS FOR CARBON CONNECTIVITY PATTERN DETERMINATION AND NMR SPECTRAL-ANALYSIS - PATCHOULOL [J].
NESZMELYI, A ;
LUKACS, G .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1981, (19) :999-1001
[6]  
SPATIL S, 1986, PESTICIDES, V30, P31
[7]  
STAMB T, 1991, ANNU REV PHYTOPATHOL, V29, P421
[8]  
TEISSEIRE P, 1980, B SOC CHEM, V2, P66