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A new protocol based on a solid-supported thiol was developed for high yielding deprotection of o-nitrobenzensulfonyl amides derived from primary and secondary amines. The reaction can be carried out at room temperature for 24 hours or accelerated by microwave irradiation, going to completion in six minutes. © Georg Thieme Verlag Stuttgart.

Cardullo, F., Donati, D., Merlo, G., Paio, A., Salaris, M., Taddei, M. (2005). Deprotection of o-Nitrobenzensulfonyl (Nosyl) Derivatives of Amines Mediated by a Solid Supported Thiol. SYNLETT(19), 2996-2998 [10.1055/s-2005-921892].

Deprotection of o-Nitrobenzensulfonyl (Nosyl) Derivatives of Amines Mediated by a Solid Supported Thiol

Taddei, Maurizio
2005-01-01

Abstract

A new protocol based on a solid-supported thiol was developed for high yielding deprotection of o-nitrobenzensulfonyl amides derived from primary and secondary amines. The reaction can be carried out at room temperature for 24 hours or accelerated by microwave irradiation, going to completion in six minutes. © Georg Thieme Verlag Stuttgart.
2005
SYNLETT
Cardullo, F., Donati, D., Merlo, G., Paio, A., Salaris, M., Taddei, M. (2005). Deprotection of o-Nitrobenzensulfonyl (Nosyl) Derivatives of Amines Mediated by a Solid Supported Thiol. SYNLETT(19), 2996-2998 [10.1055/s-2005-921892].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11365/9236
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