479064-30-7

Upstream product

• 126080-51-1 (3S,5S)-tert-butyl 3,5-dihydroxyhexanoate 
• 97037-72-4 (+)-(5S)-hydroxy-5-oxo-3-hexanoate de tert-butyle 
• 479064-29-4 Toluene-4-sulfonic acid (3R,5S)-5-benzyloxy-3-hydroxy-hexyl ester 
• 849482-18-4 ((2S,4S,6S)-6-Methyl-2-phenyl-[1,3]dioxan-4-yl)-acetic acid tert-butyl ester 
• 849482-33-3 (3R,5S)-5-Benzyloxy-hexane-1,3-diol 
• 849482-34-4 (E)-3-{(1R,3S)-3-Benzyloxy-1-[2-(toluene-4-sulfonyloxy)-ethyl]-butoxy}-2-methyl-acrylic acid methyl ester 

Downstream Products

• 479064-31-8 (S)-2-[(2S,5R)-5-((S)-2-Benzyloxy-propyl)-tetrahydro-furan-2-yl]-propionic acid methyl ester 
• 849482-27-5 (S)-2-[(2S,5R)-5-((S)-2-Hydroxy-propyl)-tetrahydro-furan-2-yl]-propionic acid (1R,3R)-3-benzyloxymethoxy-1-vinyl-pentyl ester 
• 849482-40-2 (S)-2-{(2S,5R)-5-[(S)-2-(tert-Butyl-dimethyl-silanyloxy)-propyl]-tetrahydro-furan-2-yl}-propionic acid (1R,3R)-3-benzyloxymethoxy-1-vinyl-pentyl ester 
• 849482-43-5 (E)-(1S,2S,5R,8S,9R,12S,14R)-5-((R)-2-Benzyloxymethoxy-butyl)-8-hydroxy-2,9,12-trimethyl-4,11,17-trioxa-bicyclo[12.2.1]heptadec-6-ene-3,10-dione 
• 849482-41-3 (E)-(1S,2S,5R,8R,9R,12S,14R)-5-((R)-2-Benzyloxymethoxy-butyl)-8-hydroxy-2,9,12-trimethyl-4,11,17-trioxa-bicyclo[12.2.1]heptadec-6-ene-3,10-dione 
• 849482-32-2 Benzoic acid (E)-(1R,3S,6R,7S,10R,13S,14S)-10-((R)-2-benzyloxymethoxy-butyl)-3,6,13-trimethyl-5,12-dioxo-4,11,17-trioxa-bicyclo[12.2.1]heptadec-8-en-7-yl ester 
• 849482-29-7 Benzoic acid (E)-(1R,3S,6R,7R,10R,13S,14S)-10-((R)-2-benzyloxymethoxy-butyl)-3,6,13-trimethyl-5,12-dioxo-4,11,17-trioxa-bicyclo[12.2.1]heptadec-8-en-7-yl ester 
• 849482-31-1 Benzoic acid (S)-1-[(R)-1-((S)-2-{(2R,5S)-5-[(S)-1-((1R,3R)-3-benzyloxymethoxy-1-vinyl-pentyloxycarbonyl)-ethyl]-tetrahydro-furan-2-yl}-1-methyl-ethoxycarbonyl)-ethyl]-allyl ester 
• 849482-28-6 Benzoic acid (R)-1-[(R)-1-((S)-2-{(2R,5S)-5-[(S)-1-((1R,3R)-3-benzyloxymethoxy-1-vinyl-pentyloxycarbonyl)-ethyl]-tetrahydro-furan-2-yl}-1-methyl-ethoxycarbonyl)-ethyl]-allyl ester 

Relevant academic research and scientific papers

Synthesis of the proposed structure of feigrisolide C

(Chemical Equation Presented) Possible structures of feigrisolide C were synthesized via ring-closing olefin metathesis reaction of a diester derivative prepared from 8-epinonactic acid, but physical characteristics of the synthetic samples did not match with those of the natural sample of feigrisolide C.