Herein, we describe the first enantioselective cyclopropanation of enals using benzyl chlorides as bifunctional (nucleophilic and electrophilic) reagents. The reaction is simply catalyzed by chiral secondary amines to afford the formyl cyclopropane derivatives in good yields with moderate to excellent stereoselectivities.

Meazza, M., Ashe, M., Shin, H.Y., Yang, H.S., Mazzanti, A., Yang, J.W., et al. (2016). Enantioselective Organocatalytic Cyclopropanation of Enals Using Benzyl Chlorides. JOURNAL OF ORGANIC CHEMISTRY, 81(9), 3488-3500 [10.1021/acs.joc.5b02801].

Enantioselective Organocatalytic Cyclopropanation of Enals Using Benzyl Chlorides

MAZZANTI, ANDREA;
2016

Abstract

Herein, we describe the first enantioselective cyclopropanation of enals using benzyl chlorides as bifunctional (nucleophilic and electrophilic) reagents. The reaction is simply catalyzed by chiral secondary amines to afford the formyl cyclopropane derivatives in good yields with moderate to excellent stereoselectivities.
2016
Meazza, M., Ashe, M., Shin, H.Y., Yang, H.S., Mazzanti, A., Yang, J.W., et al. (2016). Enantioselective Organocatalytic Cyclopropanation of Enals Using Benzyl Chlorides. JOURNAL OF ORGANIC CHEMISTRY, 81(9), 3488-3500 [10.1021/acs.joc.5b02801].
Meazza, Marta; Ashe, Maria; Shin, Hun Yi; Yang, Hye Sung; Mazzanti, Andrea; Yang, Jung Woon; Rios, Ramon
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/565112
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