Regioselectivity of ring-opening reactions of optically active N-acetyl-2-methoxycarbonylaziridine
摘要:
(S)-(-)-N-acetyl-2-methoxycarbonylaziridine 1 undergoes easy ring-opening by Bronsted acids or nucleophiles in the presence of a Lewis acid catalyst. The regioselectivity is not always exclusive, affording optically active alpha- and beta-aminoacids.
Regioselectivity of ring-opening reactions of optically active N-acetyl-2-methoxycarbonylaziridine
摘要:
(S)-(-)-N-acetyl-2-methoxycarbonylaziridine 1 undergoes easy ring-opening by Bronsted acids or nucleophiles in the presence of a Lewis acid catalyst. The regioselectivity is not always exclusive, affording optically active alpha- and beta-aminoacids.