The use of aziridine carboxylates as intermediates in the synthesis of optically active compounds is a subject of current interest. The ring-opening of aziridine, consequence of ring strain, is the most important feature of their chemistry and serves as the basis of the synthesis of substituted a- and /3-amino acids, which is a topic of interest in our laboratory.

Cardillo G., Casolari S., Gentilucci L., Tomasini C. (1996). Asymmetric Synthesis of AIkyl Aziridine-2-Carboxylates from Chiral 3'-Benzyloxy-aminoimides. ANGEWANDTE CHEMIE. INTERNATIONAL EDITION IN ENGLISH, 35(16), 1848-1849 [10.1002/anie.199618481].

Asymmetric Synthesis of AIkyl Aziridine-2-Carboxylates from Chiral 3'-Benzyloxy-aminoimides

Casolari S.
Investigation
;
Gentilucci L.
Investigation
;
Tomasini C.
Investigation
1996

Abstract

The use of aziridine carboxylates as intermediates in the synthesis of optically active compounds is a subject of current interest. The ring-opening of aziridine, consequence of ring strain, is the most important feature of their chemistry and serves as the basis of the synthesis of substituted a- and /3-amino acids, which is a topic of interest in our laboratory.
1996
Cardillo G., Casolari S., Gentilucci L., Tomasini C. (1996). Asymmetric Synthesis of AIkyl Aziridine-2-Carboxylates from Chiral 3'-Benzyloxy-aminoimides. ANGEWANDTE CHEMIE. INTERNATIONAL EDITION IN ENGLISH, 35(16), 1848-1849 [10.1002/anie.199618481].
Cardillo G.; Casolari S.; Gentilucci L.; Tomasini C.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/914578
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