Oxyfunctionalization of Non-Natural Targets by Dioxiranes. 4. Efficient Oxidation of Binor S Using Methyl(trifluoromethyl)dioxirane

Autor:	L, D'Accolti, C, Fusco, V, Lucchini, G B, Carpenter, R, Curci
Jazyk:	angličtina
Rok vydání:	2001
Předmět:	Ethylene Oxide Models Molecular Magnetic Resonance Spectroscopy integumentary system organic chemicals Dioxirane Crystallography X-Ray Hydroxylation Kinetics Non-Natural Targets Oxidation polycyclic compounds Indicators and Reagents Polycyclic Aromatic Hydrocarbons Oxidation-Reduction
Zdroj:	Journal of organic chemistry 66 (2001): 9063–9066. doi:10.1021/jo0109671 info:cnr-pdr/source/autori:D'Accolti L., Fusco C., Lucchini V., Carpenter Gene B., Curci R./titolo:Oxyfunctionalization of Non-Natural Targets by Dioxiranes. 4. Efficient Oxidation of Binor S Using Methyl(trifluoromethyl)dioxirane/doi:10.1021%2Fjo0109671/rivista:Journal of organic chemistry/anno:2001/pagina_da:9063/pagina_a:9066/intervallo_pagine:9063–9066/volume:66
DOI:	10.1021/jo0109671
Popis:	Methyl(trifluoromethyl)dioxirane was used to regiospecifically oxidize Binor S. Two diol and one triol products were the result.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::a2d479f9afdbaefb970ec3ba3d1ff656 https://publications.cnr.it/doc/16511 Zobrazit plný text záznamu