857285-39-3

Upstream product

• 110-87-2 3,4-dihydro-2H-pyran 
• 218434-90-3 1-but-3-ynyloxymethyl-4-methoxy-benzene 
• 204447-27-8 2-[(Z)-3-Iodo-5-(4-methoxy-benzyloxy)-pent-2-enyloxy]-tetrahydro-pyran 
• 409064-76-2 (Z)-3-Iodo-5-(4-methoxy-benzyloxy)-pent-2-en-1-ol 
• 146916-76-9 5-(4-methoxyphenyl)methoxy-2-pentyn-1-ol 
• 204447-28-9 (Z)-2-[2-(4-Methoxy-benzyloxy)-ethyl]-4-(tetrahydro-pyran-2-yloxy)-but-2-enoic acid methyl ester 

Downstream Products

• 1073861-97-8 C₂₈H₄₈O₅Si 
• 204447-34-7 (4R,5R)-5-[(Z)-8-(2-Heptyl-[1,3]dioxolan-2-yl)-oct-1-enyl]-4-[2-(4-methoxy-benzyloxy)-ethyl]-4-(4-methoxy-benzyloxymethyl)-2,2-dimethyl-[1,3]dioxane 
• 204447-36-9 {(4R,5R)-4-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-5-[(Z)-8-(2-heptyl-[1,3]dioxolan-2-yl)-oct-1-enyl]-2,2-dimethyl-[1,3]dioxan-4-yl}-methanol 
• 204447-37-0 (4R,5R)-4-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-5-[(Z)-8-(2-heptyl-[1,3]dioxolan-2-yl)-oct-1-enyl]-2,2-dimethyl-[1,3]dioxane-4-carboxylic acid methyl ester 

Relevant academic research and scientific papers

Synthesis of viridiofungin A trimethyl ester and determination of the absolute structure of viridiofungin A

Four diastereoisomeric trimethyl esters of viridiofungin A, a member of novel family of aminoacyl alkyl citrate compounds, were synthesized in a highly stereoselective manner and the absolute configuration of natural viridiofungin A was determined to be 3S,4S,2'S.