123341-20-8Relevant academic research and scientific papers
The functionalisation of electron rich aromatic compounds with 1,3-oxazolidines and 1,3-dimethylimidazolidine
Heaney, Harry,Papageorgiou, George,Wilkins, Robert F.
, p. 14381 - 14396 (2007/10/03)
N-Phenyl- and N-alkyl-oxazolidines react with alkyl chlorosilanes in the presence of electron rich aromatic compounds with the formation of the expected Mannich bases: 2-methoxycarbonyl-3-methyloxazolidine also reacts with 2-methylfuran in the presence of thionyl chloride to give an a-amino acid derivative: the iminium salt derived from 1,3-dimethylimidazolidine was also shown to react with 2-methylfuran.
MANNICH REACTIONS OF OXAZOLIDINES
Fairhurst, Robin A.,Heaney, Harry,Papageorgiou, George,Wilkins, Robert F.,Eyley, Stephen C.
, p. 1433 - 1436 (2007/10/02)
3-Methyl-1,3-oxazolidine and 3,4-dimethyl-5-phenyloxazolidine react with acidic reagents under aprotic conditions to afford reactive intermediates that interact with nucleophilic aromatic substrates and enolsilyl ethers to afford good yields of Mannich bases.
