The enantioselective organocatalytic reduction of trifluoromethyl aryl and alkyl ketoimines afforded the corresponding fluorinated amines with high chemical and stereochemical efficiency. The Lewis base catalyzed reaction with trichlorosilane led to chiral products with a trifluoromethyl group directly linked to the newly generated stereocenter typically in >90% yield and up to 98% e.e.

Stereoselective metal-free catalytic synthesis of chiral trifluoromethyl aryl and alkyl amines / A. Genoni, M. Benaglia, E. Massolo, S. Rossi. - In: CHEMICAL COMMUNICATIONS. - ISSN 1359-7345. - 49:75(2013), pp. 8365-8367. [10.1039/c3cc43821j]

Stereoselective metal-free catalytic synthesis of chiral trifluoromethyl aryl and alkyl amines

A. Genoni
Primo
;
M. Benaglia
;
E. Massolo
Penultimo
;
S. Rossi
Ultimo
2013

Abstract

The enantioselective organocatalytic reduction of trifluoromethyl aryl and alkyl ketoimines afforded the corresponding fluorinated amines with high chemical and stereochemical efficiency. The Lewis base catalyzed reaction with trichlorosilane led to chiral products with a trifluoromethyl group directly linked to the newly generated stereocenter typically in >90% yield and up to 98% e.e.
No
English
enantioselective reduction; hydrogenation; trichlorosilane; imines; access; esters
Settore CHIM/06 - Chimica Organica
Articolo
Esperti anonimi
Pubblicazione scientifica
2013
49
75
8365
8367
3
Pubblicato
Periodico con rilevanza internazionale
Aderisco
info:eu-repo/semantics/article
Stereoselective metal-free catalytic synthesis of chiral trifluoromethyl aryl and alkyl amines / A. Genoni, M. Benaglia, E. Massolo, S. Rossi. - In: CHEMICAL COMMUNICATIONS. - ISSN 1359-7345. - 49:75(2013), pp. 8365-8367. [10.1039/c3cc43821j]
open
Prodotti della ricerca::01 - Articolo su periodico
4
262
Article (author)
no
A. Genoni, M. Benaglia, E. Massolo, S. Rossi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/224670
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