244124-73-0Relevant academic research and scientific papers
Unusual access to 5-methoxy or 5,5-dimethoxy-4-methyl-3-pyrrolin-2-ones from chlorinated 4-methyl-pyrrolidin-2-ones
Bellesia, Franco,De Buyck, Laurent,Colucci, Maria V.,Ghelfi, Franco,Laureyn, Inge,Libertini, Emanuela,Mucci, Adele,Pagnoni, Ugo M.,Pinetti, Adriano,Rogge, Tina M.,Stevens, Christian V.
, p. 4573 - 4575 (2001)
The reaction of N-substituted 4-methyl-2-pyrrolidinones, carrying not less than two chlorine atoms on the C(3) and C(6) carbons afforded with alkaline methoxide in methanol, under mild conditions, the corresponding 5-methoxy or 5,5-dimethoxy-4-methyl-3-py
Synthesis of 5-methoxylated 3-pyrrolin-2-ones via the rearrangement of chlorinated pyrrolidin-2-ones
Ghelfi, Franco,Stevens, Christian V.,Laureyn, Inge,Van Meenen, Ellen,Rogge, Tina M.,De Buyck, Laurent,Nikitin, Kirill V.,Grandi, Romano,Libertini, Emanuela,Pagnoni, Ugo M.,Schenetti, Luisa
, p. 1147 - 1157 (2007/10/03)
The reaction of N-substituted 4-methyl-2-pyrrolidinones or 4-diethoxyphosphoryl analogues, carrying at least two chlorine atoms between the C(3) and C(6) carbons, with alkaline methoxide in methanol afforded the corresponding 5-methoxylated 3-pyrrolin-2-ones, useful adducts for the preparation of agrochemicals or medicinal compounds.
