Biocenversion of cyclohexene derivatives

I. Belič; E. Ghera; H. E. Gottlieb; A. Plemenitaš

doi:10.1007/BF00270591

Biocenversion of cyclohexene derivatives

I. Belič, E. Ghera, H. E. Gottlieb, A. Plemenitaš

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

1 Scopus citations

Abstract

Bioconversion of new methylcyclohexene derivatives with bulky side chains ending in aromatic or heteroaromatic rings by Streptomyces natalensis and Mycobacterium smegmatis results in monohydroxylation of the cyclohexene ring. Further oxidation of the hydroxyl group into a keto group is effected only with M. smegmatis. The synthesis of the substrates and proof of the structure of the products is given in detail.

Original language	English
Pages (from-to)	310-312
Number of pages	3
Journal	Applied Microbiology and Biotechnology
Volume	20
Issue number	5
DOIs	https://doi.org/10.1007/BF00270591
State	Published - Nov 1984
Externally published	Yes

Access to Document

10.1007/BF00270591

Cite this

@article{229821601d0e445ab86f4908fcdb3604,

title = "Biocenversion of cyclohexene derivatives",

abstract = "Bioconversion of new methylcyclohexene derivatives with bulky side chains ending in aromatic or heteroaromatic rings by Streptomyces natalensis and Mycobacterium smegmatis results in monohydroxylation of the cyclohexene ring. Further oxidation of the hydroxyl group into a keto group is effected only with M. smegmatis. The synthesis of the substrates and proof of the structure of the products is given in detail.",

author = "I. Beli{\v c} and E. Ghera and Gottlieb, {H. E.} and A. Plemenita{\v s}",

year = "1984",

month = nov,

doi = "10.1007/BF00270591",

language = "אנגלית",

volume = "20",

pages = "310--312",

journal = "Applied Microbiology and Biotechnology",

issn = "0175-7598",

publisher = "Springer Verlag",

number = "5",

}

TY - JOUR

T1 - Biocenversion of cyclohexene derivatives

AU - Belič, I.

AU - Ghera, E.

AU - Gottlieb, H. E.

AU - Plemenitaš, A.

PY - 1984/11

Y1 - 1984/11

N2 - Bioconversion of new methylcyclohexene derivatives with bulky side chains ending in aromatic or heteroaromatic rings by Streptomyces natalensis and Mycobacterium smegmatis results in monohydroxylation of the cyclohexene ring. Further oxidation of the hydroxyl group into a keto group is effected only with M. smegmatis. The synthesis of the substrates and proof of the structure of the products is given in detail.

AB - Bioconversion of new methylcyclohexene derivatives with bulky side chains ending in aromatic or heteroaromatic rings by Streptomyces natalensis and Mycobacterium smegmatis results in monohydroxylation of the cyclohexene ring. Further oxidation of the hydroxyl group into a keto group is effected only with M. smegmatis. The synthesis of the substrates and proof of the structure of the products is given in detail.

UR - http://www.scopus.com/inward/record.url?scp=0021680762&partnerID=8YFLogxK

U2 - 10.1007/BF00270591

DO - 10.1007/BF00270591

M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???

AN - SCOPUS:0021680762

SN - 0175-7598

VL - 20

SP - 310

EP - 312

JO - Applied Microbiology and Biotechnology

JF - Applied Microbiology and Biotechnology

IS - 5

ER -

Biocenversion of cyclohexene derivatives

Abstract

Access to Document

Other files and links

Fingerprint

Cite this