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.
Asymmetric Synthesis of AIkyl Aziridine-2-Carboxylates from Chiral 3'-Benzyloxy-aminoimides / Cardillo G.; Casolari S.; Gentilucci L.; Tomasini C.. - In: ANGEWANDTE CHEMIE. INTERNATIONAL EDITION IN ENGLISH. - ISSN 0570-0833. - STAMPA. - 35:16(1996), pp. 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.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
