The generation and trapping of o-thioquinones was successfully applied to the synthesis of hydroxy-4-thiaflavans on solid support using commercially available carboxy and aminomethylated polystyrene resins. These valuable cycloadducts are obtained as pure compounds without any intermediate purification, in better overall yields than the solution phase procedure.

Generation and trapping of o-thioquinones on solid support: Synthesis of hydroxylated 4-thiaflavans / S. Menichetti; C. Viglianisi. - In: PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS. - ISSN 1042-6507. - STAMPA. - 184:(2009), pp. 1233-1246. [10.1080/10426500902856339]

Generation and trapping of o-thioquinones on solid support: Synthesis of hydroxylated 4-thiaflavans

MENICHETTI, STEFANO;VIGLIANISI, CATERINA
2009

Abstract

The generation and trapping of o-thioquinones was successfully applied to the synthesis of hydroxy-4-thiaflavans on solid support using commercially available carboxy and aminomethylated polystyrene resins. These valuable cycloadducts are obtained as pure compounds without any intermediate purification, in better overall yields than the solution phase procedure.
2009
184
1233
1246
S. Menichetti; C. Viglianisi
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/368081
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