87678-99-7

Upstream product

• 32742-34-0 1,5-Anhydro-D-arabinitol 
• 85620-85-5 3R-3,6-dihydro-2H-pyranyl-N,N-dimethylacetamide 
• 87614-56-0 5S-iodo-1S,6S-3,7-dioxabicyclo<4,3,0>nonan-8-one 
• 50-69-1 D-Arabinose 
• 85620-84-4 1,5-anhydro-2,3-dideoxy-D-glycero-pent-2-enitol 
• 87614-60-6 2-{(2S,5R)-5-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-5,6-dihydro-2H-pyran-2-yl}-N,N-dimethyl-acetamide 
• 87614-59-3 (3S,4S)-3-[2-(tert-Butyl-diphenyl-silanyloxy)-ethyl]-3,4-dihydro-2H-pyran-4-ol 
• 87614-58-2 (3S,4S)-3-(2-Hydroxy-ethyl)-3,4-dihydro-2H-pyran-4-ol 
• 528869-25-2 (3S,4R,5R)-2-Bromo-tetrahydro-pyran-3,4,5-triol 
• 344569-52-4 C₃₄H₄₉NO₅Si 
• 344569-60-4 C₃₂H₄₄O₄Si 
• 344569-50-2 2-{6-[3-(tert-butyl-diphenyl-silanyloxy)-propyl]-4,5-dihydroxy-tetrahydro-pyran-3-yl}-N,N-dimethyl-acetamide 
• 344569-48-8 2-{6-[3-(tert-butyl-diphenyl-silanyloxy)-propyl]-3,6-dihydro-2H-pyran-3-yl}-N,N-dimethyl-acetamide 
• 344569-46-6 2-[3-(tert-butyl-diphenyl-silanyloxy)-propyl]-3,6-dihydro-2H-pyran-3-ol 

Downstream Products

• 12650-69-0 mupirocin 
• 71980-98-8 pseudomonic acid C 
• 87641-25-6 C₃₆H₅₀O₆Si 
• 75452-45-8 C₂₅H₄₀O₆ 
• 75452-42-5 C₃₂H₄₄O₅Si 
• 87614-61-7 C₄₀H₄₄O₇Si 

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

ENANTIOSPECIFIC TOTAL SYNTHESIS OF PSEUDOMONIC ACIDS FROM ARABINOSE

The enantiospecific synthesis of pseudomonic acids from arabinose is described.