Photosensitized oxidation of isocembrol. VII. Products of reaction at the C11 double bond

Autor:	Yu. V. Gatilov, V. A. Raldugin, V. L. Salenko, I. G. Pleshkov, N. I. Yaroshenko, S. A. Shevtsov, V. A. Pentegova
Rok vydání:	1984
Předmět:	chemistry.chemical_classification Chemical transformation Nucleophilic addition Double bond chemistry Electrophilic addition Organic chemistry Plant Science General Chemistry Medicinal chemistry General Biochemistry Genetics and Molecular Biology Bond cleavage
Zdroj:	Chemistry of Natural Compounds. 20:45-52
ISSN:	1573-8388 0009-3130
DOI:	10.1007/bf00574789
Popis:	It has been established that in the photooxidation of isocembrol, in addition to other compounds, five products of oxidation at the C11 double bond are formed, and their structures and stereochemistry have been established by chemical transformations and physicochemical methods. In the stereochemical respect, the photooxidation of isocembrol at the C11 double bond is similar to its epoxidation at the same bond.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::bb261181a3d8e23c7f1a6bcca3bbe7dc https://doi.org/10.1007/bf00574789 Zobrazit plný text záznamu Full text from SpringerLink