Direct synthesis of NH-sulfoximines from sulfides has been achieved through O and NH transfer in the same reaction, occurring with complete selectivity. The reaction is mediated by bisacetoxyiodobenzene under simple conditions and employs inexpensive N-sources. Preliminary studies indicate that NH-transfer is likely to be first, followed by oxidation, but the reaction proceeds successfully in either order. A wide range of functional groups and biologically relevant compounds are tolerated. The use of AcO15NH4 affords 15N-labeled compounds.

Synthesis of NH-sulfoximines from sulfides by chemoselective one-pot N- and O-transfers

CARLUCCI, CLAUDIA;
2017-01-01

Abstract

Direct synthesis of NH-sulfoximines from sulfides has been achieved through O and NH transfer in the same reaction, occurring with complete selectivity. The reaction is mediated by bisacetoxyiodobenzene under simple conditions and employs inexpensive N-sources. Preliminary studies indicate that NH-transfer is likely to be first, followed by oxidation, but the reaction proceeds successfully in either order. A wide range of functional groups and biologically relevant compounds are tolerated. The use of AcO15NH4 affords 15N-labeled compounds.
2017
Inglese
Inglese
53
2
348
351
4
www.rsc.org/chemcomm
Esperti anonimi
Catalysis
Electronic
Optical and Magnetic Materials
Ceramics and Composites
Chemistry (all)
Surfaces
Coatings and Films
2506
Materials Chemistry2506 Metals and Alloys
9
info:eu-repo/semantics/article
262
Tota, Arianna; Zenzola, Marina; Chawner, Stephen J.; John Campbell, Sahra St; Carlucci, Claudia; Romanazzi, Giuseppe; Degennaro, Leonardo; Bull, James...espandi
1 Contributo su Rivista::1.1 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14085/19950
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