Приказ основних података о документу

dc.creatorStefanović, Milutin
dc.creatorLajšić, Stevan D.
dc.date.accessioned2021-05-23T16:57:00Z
dc.date.available2021-05-23T16:57:00Z
dc.date.issued1967
dc.identifier.issn0040-4039
dc.identifier.urihttps://cer.ihtm.bg.ac.rs/handle/123456789/4661
dc.description.abstractA number of selective reductions using borane end metal borohydrides has been described. In our studies of hydroboration of steroid conjugated ketones under different conditions and with different solvents we have found that borane reduces in a good yield the carbonyl group in C-3 of progesterone, without affecting the carbonyl in C-20, as well as the Delta4 double bound, thus giving as the main product, 3beta-hydroxy- 20-keto-Delta4-pregnene, which was obtained in a pure state by direct crystallization of the reaction product from methanol.sr
dc.language.isoensr
dc.publisherElseviersr
dc.rightsrestrictedAccesssr
dc.sourceTetrahedron Letterssr
dc.subjectboranesr
dc.subjectprogesteronesr
dc.subjectboric acidsr
dc.subjectoxidation reduction reactionsr
dc.titleSelective borane reductions of progesteronesr
dc.typearticlesr
dc.rights.licenseARRsr
dcterms.abstractСтефановић, Милутин; Лајшић, Стеван Д.; Селецтиве боране редуцтионс оф прогестероне; Селецтиве боране редуцтионс оф прогестероне;
dc.citation.volume8
dc.citation.issue19
dc.citation.spage1777
dc.citation.epage1779
dc.identifier.pmid6047532
dc.identifier.doi10.1016/S0040-4039(00)90721-4
dc.identifier.scopus2-s2.0-0014086295
dc.type.versionpublishedVersionsr


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Приказ основних података о документу