The synthesis of 1,3-oxathiolanes from carbonyl compounds has been performed in good yields using Amberlyst®15 as a convenient, reusable, heterogeneous catalyst. The procedure can be applied for the chemoselective protection of aldeydes in the presence of a ketone function. In addition, Amberlyst®l5 can be recycled without loss of activity and can be even employed in the regeneration of carbonyl group.

Amberlyst® 15 as a mild, chemoselective and reusable heterogeneous catalyst for the conversion of carbonyl compounds to 1,3-oxathiolanes / Ballini R.; Bosica G.; Maggi R.; Mazzacani A.; Righi P.; Sartori G.. - In: SYNTHESIS. - ISSN 0039-7881. - STAMPA. - 2001:12(2001), pp. 1826-1829. [10.1055/s-2001-17532]

Amberlyst® 15 as a mild, chemoselective and reusable heterogeneous catalyst for the conversion of carbonyl compounds to 1,3-oxathiolanes

Righi P.;
2001

Abstract

The synthesis of 1,3-oxathiolanes from carbonyl compounds has been performed in good yields using Amberlyst®15 as a convenient, reusable, heterogeneous catalyst. The procedure can be applied for the chemoselective protection of aldeydes in the presence of a ketone function. In addition, Amberlyst®l5 can be recycled without loss of activity and can be even employed in the regeneration of carbonyl group.
2001
Amberlyst® 15 as a mild, chemoselective and reusable heterogeneous catalyst for the conversion of carbonyl compounds to 1,3-oxathiolanes / Ballini R.; Bosica G.; Maggi R.; Mazzacani A.; Righi P.; Sartori G.. - In: SYNTHESIS. - ISSN 0039-7881. - STAMPA. - 2001:12(2001), pp. 1826-1829. [10.1055/s-2001-17532]
Ballini R.; Bosica G.; Maggi R.; Mazzacani A.; Righi P.; Sartori G.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/893906
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