Synlett, Journal Year: 2025, Volume and Issue: unknown
Published: April 8, 2025
Abstract The synthesis of N-alkylated oxindoles remains an important focus in organic chemistry, due to their common occurrence bioactive compounds and pharmaceutical agents. An efficient novel strategy for alkylating the oxindole scaffold at N-1 position is described. By using (N-methylpyrrol-2-yl)methylidene as a protecting group competing C-3 position, this methodology provides simple mild procedure convert various into corresponding N-benzylated derivatives moderate good overall yields (up 67%).
Language: Английский