254730-10-4

Upstream product

• 254730-08-0 (S)-4-Benzyloxy-5-(3-benzyloxy-propyl)-5-hydroxy-1-(4-methoxy-benzyl)-pyrrolidin-2-one 
• 254730-07-9 (S)-4-benzyloxy-1-(4-methoxybenzyl)-2,5-pyrrolidinedione 
• 254730-06-8 (S)-4-hydroxy-1-(4-methoxybenzyl)-2,5-pyrrolidinedione 
• 174874-82-9 acetic acid (3S)-1-(4-methoxy-benzyl)-2,5-dioxo-pyrrolidin-3-yl ester 
• 254730-09-1 (+)-(4S,5R)-4-benzyloxy-5-(3'-benzyloxypropyl)-1-(4-methoxybenzyl)-2-pyrrolidinone 

Downstream Products

• 254730-11-5 C₂₉H₃₃NO₈S₂ 
• 254730-12-6 C₂₁H₂₅NO₇S₂ 
• 126424-76-8 pyrrolam A 

Relevant academic research and scientific papers

Asymmetric synthesis of (-)-(R)-pyrrolam A starting from (S)-malic acid

An asymmetric synthesis of natural (-)-pyrrolam A starting from natural (S)-malic acid is described. The stereogenic center was established via a highly trans-diastereoselective reductive alkylation procedure. A tandem base-induced intramolecular amide N-