The hetero-Michael reactions between various oxygen, sulphur and nitrogen nucleophiles and α,β-unsaturated compounds were carried out in the presence of catalytic amounts of o-benzenedisulfonimide as Brønsted acid organocatalyst. The reaction conditions were very mild and the yields of target products were good. The catalyst was easily recovered and purified, ready to be used in further reactions. This ability grants economic and ecological advantages.

o-Benzenedisulfonimide as a Reusable Brønsted Acid Catalyst for Hetero-Michael Reactions

BARBERO, Margherita;CADAMURO, Silvano;DUGHERA, Stefano
2013-01-01

Abstract

The hetero-Michael reactions between various oxygen, sulphur and nitrogen nucleophiles and α,β-unsaturated compounds were carried out in the presence of catalytic amounts of o-benzenedisulfonimide as Brønsted acid organocatalyst. The reaction conditions were very mild and the yields of target products were good. The catalyst was easily recovered and purified, ready to be used in further reactions. This ability grants economic and ecological advantages.
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http://www.tandfonline.com/toc/lsyc20/current#.UYJ2mkqdB_M
Brønsted acid; conjugate addition; homogeneous catalysis; Michael reaction; recyclable catalyst
Margherita Barbero; Silvano Cadamuro; Stefano Dughera
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/91289
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