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- W2068113603 abstract "The λ3-iodane [bis(trifluoroacetoxy)]iodobenzene (BTI)-mediated oxidative dearomatization of 2-alkoxyarenols with soft external carbon-based nucleophiles constitutes a rapid access to highly functionalized naphthoid cyclohexa-2,4-dienones. These synthons can serve as valuable intermediates in the construction of the angularly-oxygenated benz[a]naphthalene ABC ring system of aquayamycin- and SS-228Y-type antibiotic angucyclinones, and analogues thereof. This methodology led to the elaboration of five-membered A ring-containing analogues of this ABC tricyclic unit. In addition, the BTI-mediated oxidative activation of 2-methylnaphthol can be exploited to prepare menadione (i.e. vitamin K3), known to induce apoptosis and autoschizis, a novel type of cancer cell death." @default.
- W2068113603 created "2016-06-24" @default.
- W2068113603 creator A5017115973 @default.
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- W2068113603 creator A5043428400 @default.
- W2068113603 creator A5080723398 @default.
- W2068113603 creator A5080843788 @default.
- W2068113603 date "2005-02-01" @default.
- W2068113603 modified "2023-09-27" @default.
- W2068113603 title "λ3-Iodane-mediated arenol dearomatization. Synthesis of five-membered ring-containing analogues of the aquayamycin ABC tricyclic unit and novel access to the apoptosis inducer menadione" @default.
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