477772-16-0

Upstream product

• 586-75-4 4-chlorobenzoyl chloride 
• 477772-14-8 3a-(tert-butyl-dimethyl-silanyloxymethyl)-6a-ethyl-6-hydroxy-tetrahydro-furo[3,2-b]furan-2-one 
• 477772-11-5 (R)-2,2-Dimethyl-4-[(R)-1-(5-trimethylsilanyl-furan-3-yl)-1-trimethylsilanyloxy-propyl]-[1,3]dioxolane 
• 477772-12-6 4-[(R)-1-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-1-trimethylsilanyloxy-propyl]-5H-furan-2-one 
• 477772-10-4 [(R)-1-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-1-furan-3-yl-propoxy]-trimethyl-silane 
• 477772-13-7 4-((1R,2R)-1-Ethyl-1,2,3-trihydroxy-propyl)-5H-furan-2-one 
• 403665-44-1 (R)-1-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-1-furan-3-yl-propan-1-ol 

Downstream Products

• 477772-17-1 4-Bromo-benzoic acid (3R,3aS,6aR)-3a-ethyl-6a-hydroxymethyl-5-oxo-hexahydro-furo[3,2-b]furan-3-yl ester 

Relevant academic research and scientific papers

An enantioselective synthetic pathway towards plakortones

An enantioselective synthesis of functionalized bicyclic lactones 2, 3 and 4, core structures of plakortones, are described; the configurations of 2,3 and 4 were confirmed by X-ray crystallographic analyses of their precursors 11, 19 and 24, respectively.