Epoxidation of double bond was the main reaction performed by Zoophthora (Erynia) ovispora on methyl and ethyl alpha-campholenyl ketones 1 and 6. Apart from epoxides 2, 3, 7, and 8, some other products were isolated, with additional oxygen function in alpha-position to the double bond (9 and 10). The presence of the BAEYER-VILLIGER reaction product (4) and diketone 11 is also postulated.
Microbial Transformation of Isoprenoid Systems By Means of Zoophthora (erynia) Ovispora (nowakowski) Batko
GRASSI, Alfonso
1993
Abstract
Epoxidation of double bond was the main reaction performed by Zoophthora (Erynia) ovispora on methyl and ethyl alpha-campholenyl ketones 1 and 6. Apart from epoxides 2, 3, 7, and 8, some other products were isolated, with additional oxygen function in alpha-position to the double bond (9 and 10). The presence of the BAEYER-VILLIGER reaction product (4) and diketone 11 is also postulated.File in questo prodotto:
Non ci sono file associati a questo prodotto.
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
