Please use this identifier to cite or link to this item: https://dspace.upt.ro/xmlui/handle/123456789/1542
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dc.contributor.authorFăgădar-Cosma, Eugenia-
dc.contributor.authorMagda, Angela-
dc.date.accessioned2020-04-10T09:09:34Z-
dc.date.accessioned2021-03-01T08:36:55Z-
dc.date.available2020-04-10T09:09:34Z-
dc.date.available2021-03-01T08:36:55Z-
dc.date.issued2006-
dc.identifier.citationFăgădar-Cosma, Eugenia Lenuţa. Ring phosphorus (V) compounds obtained from p-isopropyl-phenyldichlorophosphine. Synthesis, stereoisomerism and biological activity. Timişoara: Editura Politehnica, 2006en_US
dc.identifier.urihttp://primo.upt.ro:1701/primo-explore/search?query=any,contains,Ring%20phosphorus%20(V)%20compounds%20obtained%20from%20p-isopropyl-phenyldichlorophosphine.%20Synthesis,%20stereoisomerism%20and%20biological%20activity&tab=default_tab&search_scope=40TUT&vid=40TUT_V1&lang=ro_RO&offset=0 Link Primo-
dc.description.abstractIn connection to our previous reports[1] regarding the auxine like effects of some phosphorin-2-oxide ring compounds, this study was concerned about a Mannich type syntheses involving p-isopropyl-phenyldichlorophosphine, o-aminophenol, 1,2-diaminopropan and acetone. A discussion about the products of the reactions, that are in fact a mixture of diastereomers, because of the existence of some stereogenic sites at the phosphorus and carbon atoms, was done.The newly obtained heterocyclic compounds were investigated regarding the development of chlorophyll a and b contents, in plants treated with different concentrations of the above-mentioned substances.en_US
dc.language.isoenen_US
dc.publisherTimişoara: Editura Politehnicaen_US
dc.relation.ispartofseriesSeria chimie şi ingineria mediului, Tom 51(65), fasc. 1-2 (2006)-
dc.subjectp-Isopropyl-phenyldichlorophosphineen_US
dc.subjectMannich reactionen_US
dc.subjectStereogenic sitesen_US
dc.subjectChlorophyll aen_US
dc.subjectAuxine effecten_US
dc.subjectChlorophyll b-
dc.titleRing phosphorus (V) compounds obtained from p-isopropyl-phenyldichlorophosphine. Synthesis, stereoisomerism and biological activity [articol]en_US
dc.typeArticleen_US
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