In:
Zeitschrift für Naturforschung C, Walter de Gruyter GmbH, Vol. 55, No. 5-6 ( 2000-6-1), p. 341-346
Abstract:
Ambrox (1), a perfumery diterpene, was oxidatively metabolised by a plant pathogenic fungus Botrytis cinerea in a xenobiotic fashion to afford a major product, i.e., 1β-hydroxy-8- epiambrox (13) (60% ) along with three minor metabolites 3β-hydroxyambrox (2), sclareolide (5) and 3β-hydroxysclareolide (7). Sclareolide (5), a cytotoxic diterpenoidal lactone was fermented with the same fungus to yield 3β-hydroxysclareolide (7) (59% ) as a major metabolite together with two minor metabolites characterised as 1-ketosclareolide (15), and 3β,14-dihydroxysclareolide (16).
Type of Medium:
Online Resource
ISSN:
1865-7125
,
0939-5075
DOI:
10.1515/znc-2000-5-608
Language:
English
Publisher:
Walter de Gruyter GmbH
Publication Date:
2000
detail.hit.zdb_id:
2078107-6
SSG:
12
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