344569-48-8

Upstream product

• 344569-34-2 ((1R,2S,5S,7R)-2-Allyloxy-6,8-dioxa-bicyclo[3.2.1]oct-7-ylmethoxy)-tert-butyl-dimethyl-silane 
• 344569-38-6 (1R,2S,5R,7S)-2-Allyloxy-7-iodomethyl-6,8-dioxa-bicyclo[3.2.1]octane 
• 344569-36-4 ((1R,2S,5S,7R)-2-Allyloxy-6,8-dioxa-bicyclo[3.2.1]oct-7-yl)-methanol 
• 344569-42-2 (4S,5S)-4-Allyloxy-hept-6-ene-1,5-diol 
• 344569-44-4 (2S,3S)-2-(3-Hydroxy-propyl)-3,6-dihydro-2H-pyran-3-ol 
• 344569-32-0 (1R,2S,5S,7R)-7-(tert-Butyl-dimethyl-silanyloxymethyl)-6,8-dioxa-bicyclo[3.2.1]octan-2-ol 
• 221015-49-2 (1R,2S,5S,7R)-7-(tert-Butyl-dimethyl-silanyloxymethyl)-6,8-dioxa-bicyclo[3.2.1]oct-3-en-2-ol 
• 221015-46-9 (1S,5S,7R)-7-(tert-Butyl-dimethyl-silanyloxymethyl)-6,8-dioxa-bicyclo[3.2.1]oct-3-en-2-one 
• 18871-66-4 N,N-dimethylacetamide dimethyl acetal 
• 344569-46-6 2-[3-(tert-butyl-diphenyl-silanyloxy)-propyl]-3,6-dihydro-2H-pyran-3-ol 

Downstream Products

• 344569-52-4 C₃₄H₄₉NO₅Si 
• 344569-60-4 C₃₂H₄₄O₄Si 
• 75452-42-5 C₃₂H₄₄O₅Si 
• 87678-99-7 1-{(2S,3R,4R,5S)-5-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-3,4-dihydroxy-tetrahydro-pyran-2-yl}-propan-2-one 
• 344569-50-2 2-{6-[3-(tert-butyl-diphenyl-silanyloxy)-propyl]-4,5-dihydroxy-tetrahydro-pyran-3-yl}-N,N-dimethyl-acetamide 

Relevant academic research and scientific papers

A diastereocontrolled route to the tetrahydropyran nucleus of pseudomonic acids

A diastereocontrolled synthesis of the tetrahydropyran nucleus of pseudomonic acids has been achieved starting from a chiral building block, which we have developed. The key step is a convex-face reduction of the block having a biased framework which allo