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- W2915999627 endingPage "3048" @default.
- W2915999627 startingPage "3043" @default.
- W2915999627 abstract "A mild and atom-economic method was developed for direct and efficient synthesis of quinazolinones through a transition-metal-free aerobic oxidative cascade annulation reaction of widely available o-aminoarylnitriles and alcohols. Air could be employed as an effective oxidant under mild conditions, generating water as the only byproduct. Possibly owing to the cesium effect, the water-soluble base CsOH was found to be crucial in all key steps of the reaction mechanism. Because a wide range of substrates can be used to prepare substituted quinazolinones without contamination by transition-metal residues, this method may be of interest for application in pharmaceutical synthesis. Possible reaction paths were also proposed according to control reactions." @default.
- W2915999627 created "2019-03-02" @default.
- W2915999627 creator A5000238995 @default.
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- W2915999627 creator A5031426033 @default.
- W2915999627 creator A5040991307 @default.
- W2915999627 creator A5073411346 @default.
- W2915999627 date "2019-03-07" @default.
- W2915999627 modified "2023-10-16" @default.
- W2915999627 title "Efficient Synthesis of Quinazolinones by Transition‐Metal‐Free Direct Aerobic Oxidative Cascade Annulation of Alcohols with<i>o</i>‐Aminoarylnitriles" @default.
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