Acetoxylation of steroidal lactones by means of lead tetraacetate

dc.creator	Stefanović, Milutin
dc.creator	Djarmati, Z
dc.creator	Gašić, Miroslav
dc.date.accessioned	2021-05-26T13:06:10Z
dc.date.available	2021-05-26T13:06:10Z
dc.date.issued	1970
dc.identifier.issn	0040-4039
dc.identifier.issn	1873-3581
dc.identifier.uri	https://cer.ihtm.bg.ac.rs/handle/123456789/4664
dc.description.abstract	One of the structural features of many bitter principles ls the presence of a &-lactone ring. Some of these compounds differ from one another by the state of oxidation of the molecule as a whole and also by the state of oxidation of the lactone ring (Le. chaparrin-glauca rubol) (1). However, the correlation of these compound by direct introduction of an oxygen function Into the lactone ring by chemical means represents a great difficulty.	sr
dc.language.iso	en	sr
dc.publisher	Elsevier	sr
dc.rights	restrictedAccess	sr
dc.source	Tetrahedron Letters	sr
dc.subject	Acetoxylation	sr
dc.subject	steroidal lactones	sr
dc.subject	lead tetraacetate	sr
dc.title	Acetoxylation of steroidal lactones by means of lead tetraacetate	sr
dc.type	article	sr
dc.rights.license	ARR	sr
dcterms.abstract	Гашић, Мирослав; Стефановић, Милутин; Дјармати, З;
dc.citation.volume	11
dc.identifier.doi	10.1016/S0040-4039(01)98337-6
dc.identifier.scopus	2-s2.0-49849112739
dc.type.version	publishedVersion	sr