Anchimeric Assistance in the N-Alkylation of 5-alkoxymethyl-2-pyrrolidinone Derivatives
- 1 November 1992
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 22 (20) , 2935-2940
- https://doi.org/10.1080/00397919208021117
Abstract
5-Substituted 2-pyrrolidinones are normally difficult to alkylate at nitrogen. The presence of an alkoxymethyl group at C5, however, facilitates alkylation by a neighboring group effect.Keywords
This publication has 4 references indexed in Scilit:
- An Improved Reduction of the Ester Moiety in N-Substituted PyroglutamatesSynthetic Communications, 1989
- Syntheses of (S)-5-substituted 4-aminopentanoic acids: a new class of .gamma.-aminobutyric acid transaminase inactivatorsThe Journal of Organic Chemistry, 1980
- N-Alkylation of Lactams with Phase Transfer CatalystHETEROCYCLES, 1979
- The Hydrogenation of Esters to Alcohols at 25-150°Journal of the American Chemical Society, 1948