Isolation and biosynthesis of ergosta-5,7,9(11),22-tetraen-3β-ol from Mucor rouxii

L. Atherton; J. M. Duncan; S. Safe

doi:10.1039/C39720000882

Isolation and biosynthesis of ergosta-5,7,9(11),22-tetraen-3β-ol from Mucor rouxii

L. Atherton, J. M. Duncan, S. Safe

Research output: Contribution to journal › Article › peer-review

10 Scopus citations

Abstract

Biosynthetic studies have shown that ergosta-5,7,9(11),22-tetraen-3β- ol, isolated from the fungus Mucor rouxii, is derived from ergosterol presumbaly via a biological dehydrogenation (oxidation) reaction.

Original language	English (US)
Pages (from-to)	882-883
Number of pages	2
Journal	Journal of the Chemical Society, Chemical Communications
Volume	0
Issue number	15
DOIs	https://doi.org/10.1039/C39720000882
State	Published - 1972

ASJC Scopus subject areas

Molecular Medicine

Access to Document

10.1039/C39720000882

Cite this

@article{0906dbfd581940c795dbaa315eed8280,

title = "Isolation and biosynthesis of ergosta-5,7,9(11),22-tetraen-3β-ol from Mucor rouxii",

abstract = "Biosynthetic studies have shown that ergosta-5,7,9(11),22-tetraen-3β- ol, isolated from the fungus Mucor rouxii, is derived from ergosterol presumbaly via a biological dehydrogenation (oxidation) reaction.",

author = "L. Atherton and Duncan, \{J. M.\} and S. Safe",

year = "1972",

doi = "10.1039/C39720000882",

language = "English (US)",

volume = "0",

pages = "882--883",

journal = "Journal of the Chemical Society, Chemical Communications",

issn = "0022-4936",

publisher = "Chemical Society",

number = "15",

}

TY - JOUR

T1 - Isolation and biosynthesis of ergosta-5,7,9(11),22-tetraen-3β-ol from Mucor rouxii

AU - Atherton, L.

AU - Duncan, J. M.

AU - Safe, S.

PY - 1972

Y1 - 1972

N2 - Biosynthetic studies have shown that ergosta-5,7,9(11),22-tetraen-3β- ol, isolated from the fungus Mucor rouxii, is derived from ergosterol presumbaly via a biological dehydrogenation (oxidation) reaction.

AB - Biosynthetic studies have shown that ergosta-5,7,9(11),22-tetraen-3β- ol, isolated from the fungus Mucor rouxii, is derived from ergosterol presumbaly via a biological dehydrogenation (oxidation) reaction.

UR - https://www.scopus.com/pages/publications/37049140074

UR - https://www.scopus.com/inward/citedby.url?scp=37049140074&partnerID=8YFLogxK

U2 - 10.1039/C39720000882

DO - 10.1039/C39720000882

M3 - Article

AN - SCOPUS:37049140074

SN - 0022-4936

VL - 0

SP - 882

EP - 883

JO - Journal of the Chemical Society, Chemical Communications

JF - Journal of the Chemical Society, Chemical Communications

IS - 15

ER -

Isolation and biosynthesis of ergosta-5,7,9(11),22-tetraen-3β-ol from Mucor rouxii

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this