603127-07-7

Upstream product

• 603127-00-0 (3S,4R,5S)-3,4-Bis-benzyloxy-1-(4-methoxy-benzyl)-5-((S)-11-methoxymethoxy-13-methyl-tetradec-1-ynyl)-pyrrolidin-2-one 
• 603127-06-6 (2S,3R,4S)-3,4-Bis-benzyloxy-2-((S)-11-methoxymethoxy-13-methyl-tetradec-1-ynyl)-5-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 100-39-0 benzyl bromide 
• 603127-01-1 (2S,3R,4S)-3,4-Dihydroxy-2-((S)-11-methoxymethoxy-13-methyl-tetradecyl)-5-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester 

Downstream Products

• 135574-63-9 penaresidin B 
• 603127-08-8 [(1S,12S)-1-((1R,2R)-2-Benzyloxy-3-hydroxy-1-methoxymethoxy-propyl)-12-methoxymethoxy-14-methyl-pentadecyl]-carbamic acid tert-butyl ester 
• 603127-09-9 [(1S,12S)-1-((1R,2R)-2-Benzyloxy-1,3-bis-methoxymethoxy-propyl)-12-methoxymethoxy-14-methyl-pentadecyl]-carbamic acid tert-butyl ester 
• 603127-02-2 (3S,4R,5S)-3-Benzyloxy-4-methoxymethoxy-5-((S)-11-methoxymethoxy-13-methyl-tetradecyl)-2-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester 

Relevant academic research and scientific papers

Novel and practical asymmetric synthesis of an azetidine alkaloid, penaresidin B

A novel and efficient asymmetric synthesis of the potent actomyosin ATPase activator, penaresidin B, is described in a short and complete stereoselective manner by featuring the elaboration of the fully functionalized homochiral lactam, which can also be