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Microbial transformation of isoprenoid systems by means of Zoophthora (Erynia) ovispora (NOWAKOWSKI) BATKO

✍ Scribed by Jerzy M. Urbańczyk; Jadwiga Sołoducho; Prof. Dr. Andrzej Zabźa; Guido Sodano; Alfonso Grassi


Publisher
John Wiley and Sons
Year
1993
Tongue
English
Weight
450 KB
Volume
33
Category
Article
ISSN
0233-111X

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✦ Synopsis


Epoxidation of double bond was the main reaction performed by Zoophthora (Erynia) ovispora on methyl and ethyl a-campholenyl ketones 1 and 6. Apart from epoxides 2, 3, 7, and 8, some other products were isolated, with additional oxygen function in a-position to the double bond (9 and 10). The presence of the BAEYER-VILLIGER reaction product (4) and diketone 11 is also postulated.


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