1421322-46-4

Upstream product

• 1421322-44-2 [(3S,4S)-4-acetyl-1-(4-methoxybenzyl)-2-oxopyrrolidin-3-yl] acetic acid 
• 2393-23-9 4-methoxy-benzylamine 
• 1421322-42-0 2-bromo-N-(3-oxobutyl)acetamide-1-ethyl-4-methoxybenzene 
• 1421322-45-3 ethyl [(3S,4S)-4-acetyl-1-(4-methoxybenzyl)-2-oxopyrrolidin-3-yl]acetate 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 1421322-41-9 C₁₂H₁₇NO₂ 

Relevant academic research and scientific papers

Synthetic studies of alkaloids containing pyrrolidine and piperidine structural motifs

Avenues to asymmetric alkaloids! Various 2-substituted pyrrolidine and piperidine chiral bioactive natural products were synthesized using a 'chiral pool' method. l-proline and l-pipecolinic acids with one chiral center served as the best precursors for the synthesis of these alkaloids. Overall, 14 total synthetic and 11 formal synthetic approaches were developed.

Tandem approaches for the synthesis of functionalized pyrrolidones: Efficient routes toward allokainic acid and kainic acid

Tandem approaches for the synthesis of pyrrolidone precursor of allokainic acid and kainic acid are described. The synthesis of pyrrolidone intermediate of allokainic acid is achieved by tandem Wittig-Michael reaction and tandem amidation-Michael reaction