http://www.cnr.it/ontology/cnr/individuo/prodotto/ID16720
Selective oxidation of acetylenic 1,4-diols with Dioxiranes in comparison with the Methyltrioxorhenium-Hydrogen Peroxide oxidant (Articolo in rivista)
- Type
- Label
- Selective oxidation of acetylenic 1,4-diols with Dioxiranes in comparison with the Methyltrioxorhenium-Hydrogen Peroxide oxidant (Articolo in rivista) (literal)
- Anno
- 2004-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1016/j.tetlet.2004.09.110 (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- D'Accolti L.; Fiorentino M.; Fusco C.; Crupi P.; Curci R (literal)
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- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Dipartimento Chimica, Università di Bari, C.N.R.--Istituto di Chimica dei Composti Organometallici (ICCOM) (literal)
- Titolo
- Selective oxidation of acetylenic 1,4-diols with Dioxiranes in comparison with the Methyltrioxorhenium-Hydrogen Peroxide oxidant (literal)
- Abstract
- Dimethyldioxirane and its trifluoro analog were employed to achieve selectively the direct transformation of hex-3-yne-2,5-diol and 1,4-diphenyl-2-butyne-1,4-diol into carbonyls, e.g., I (R = Me, Ph), leaving the carbon-carbon triple bond moiety untouched. The results were compared with those recorded in the analogous oxidn. using the methyltrioxorhenium/H2O2 homogeneous system. The powerful methyl(trifluoromethyl)dioxirane was the reagent of choice to achieve optimum yields of the target alkyne-1,4-diones, which were extremely versatile synthons. (literal)
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