We have described the first organocatalytic stereoselective formylation of ketones accomplished by the use of N-methybenzothiazolylium iodide. The benzothiazolium salt, generally used as a masked formyl group or as precursor of carbenes,[31] is quite electrophilic and react with enamines formed in situ. Both moderate yield and high stereoselectivity were obtained with different ketones.

Organocatalytic Stereoselective α-Formylation of Ketones / Capdevila, M G; Emer, E; Gualandi, A; Petruzziello, D; Grilli, S; Cozzi, P G. - In: CHEMCATCHEM. - ISSN 1867-3880. - STAMPA. - 4:7(2012), pp. 968-971. [10.1002/cctc.201200122]

Organocatalytic Stereoselective α-Formylation of Ketones

GUALANDI, ANDREA;GRILLI, STEFANO;COZZI, PIER GIORGIO
2012

Abstract

We have described the first organocatalytic stereoselective formylation of ketones accomplished by the use of N-methybenzothiazolylium iodide. The benzothiazolium salt, generally used as a masked formyl group or as precursor of carbenes,[31] is quite electrophilic and react with enamines formed in situ. Both moderate yield and high stereoselectivity were obtained with different ketones.
2012
Organocatalytic Stereoselective α-Formylation of Ketones / Capdevila, M G; Emer, E; Gualandi, A; Petruzziello, D; Grilli, S; Cozzi, P G. - In: CHEMCATCHEM. - ISSN 1867-3880. - STAMPA. - 4:7(2012), pp. 968-971. [10.1002/cctc.201200122]
Capdevila, M G; Emer, E; Gualandi, A; Petruzziello, D; Grilli, S; Cozzi, P G
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/122075
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