733000-66-3

Upstream product

• 870-63-3 prenyl bromide 
• 733000-60-7 (S)-2-((R)-2-Benzyloxy-1-hydroxy-ethyl)-5-methyl-hex-4-enoic acid ethyl ester 
• 733000-64-1 (S)-2-[(R)-2-Benzyloxy-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-5-methyl-hex-4-enoic acid methoxy-methyl-amide 
• 733000-65-2 (S)-5-[(R)-2-Benzyloxy-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2-methyl-tetradec-2-en-6-one 
• 106058-91-7 (+)-(R)-ethyl 4-benzyloxy-3-hydroxybutanoate 
• 3314-49-6 octyllithium 
• 733000-63-0 (S)-5-((R)-2-Benzyloxy-1-hydroxy-ethyl)-2-methyl-tetradec-2-en-6-one 

Relevant academic research and scientific papers

An efficient ruthenium-catalyzed formal synthesis of (-)-isoavenaciolide

A formal synthesis of (-)-isoavenaciolide (1) by two different routes is reported. The first approach, leading to a key precursor 2 of (-)-isoavenaciolide (1), features the stereoselective construction of the three contiguous stereogenic centers by Evans