116706-51-5

Upstream product

• 116706-46-8 2-<(1S,2E)-1-methoxy-2-butenyl>-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 116706-50-4 (2S,3S,4S,5S)-5-(tert-Butyldimethylsilyloxy)-3-(p-methoxybenzyloxy)-2,4-dimethylheptanal 

Downstream Products

• 135393-87-2 (2R,4R,5R,6R)-4-<(1S,2S)-2-(tert-Butyldimethylsiloxy)-1-methylbutyl>-6-<(1R,2Z)-3-methoxy-1-methyl-2-propenyl>-2-(p-methoxyphenyl)-5-methyl-1,3-dioxane 
• 135393-92-9 (2S,4S,6R,8E)-2-((2S,4S,5S,6R)-6-<(1S,2S)-2-(tert-Butyldimethylsilyloxy)-1-methylbutyl>-2-(p-methoxyphenyl)-5-methyl-1,3-dioxan-4-yl)-3-hydroxy-4,6,8-trimethyl-8-undecen-3,5-dione 
• 135501-24-5 (2S,4R,6R,8E)-2-((2S,4S,5S,6R)-6-<(1S,2S)-2-(tert-Butyldimethylsilyloxy)-1-methylbutyl>-2-(p-methoxyphenyl)-5-methyl-1,3-dioxan-4-yl)-3-hydroxy-4,6,8-trimethyl-8-undecen-3,5-dione 
• 135501-21-2 (2S,4RS,6S,8E)-2-((2S,4S,5S,6R)-6-<(1S,2S)-2-(tert-Butyldimethylsilyloxy)-1-methylbutyl>-2-(p-methoxyphenyl)-5-methyl-1,3-dioxan-4-yl)-3-hydroxy-4,6,8-trimethyl-8-undecen-3,5-dione 
• 135501-20-1 (2R,3S,4R,6S,8E)-2-((2R,4R,5R,6R)-6-<(1S,2S)-2-(tert-Butyldimethylsilyloxy)-1-methylbutyl>-2-(p-methoxyphenyl)-5-methyl-1,3-dioxan-4-yl)-3-hydroxy-4,6,8-trimethyl-8-undecen-5-one 
• 135501-19-8 (2R,3S,4R,6R,8E)-2-((2R,4R,5R,6R)-6-<(1S,2S)-2-(tert-Butyldimethylsilyloxy)-1-methylbutyl>-2-(p-methoxyphenyl)-5-methyl-1,3-dioxan-4-yl)-3-hydroxy-4,6,8-trimethyl-8-undecen-5-one 
• 135393-89-4 (2S,4RS,6R,8E)-2-((2S,4S,5S,6R)-2-(p-Methoxyphenyl)-5-methyl-6-<(1S)-1-methyl-2-oxobutyl>-1,3-dioxan-4-yl)-4,6,8-trimethyl-8-undecen-3,5-dione 
• 135393-93-0 (2R,3S,4R,6R,8E)-2-((2S,4R,5S,6S)-6-<(1R,2S)-2-Hydroxy-1-methylbutyl>-2-(p-methoxyphenyl)-5-methyl-1,3-dioxan-4-yl)-3-hydroxy-4,6,8-trimethyl-8-undecen-5-one 
• 135393-99-6 (2S)-2-((2S,4S,5S,6R)-6-<(1S,2S)-2-(tert-Butyldimethylsilyloxy)-1-methylbutyl>-2-(p-methoxyphenyl)-5-methyl-1,3-dioxan-4-yl)propanal 

Relevant academic research and scientific papers

Stereoselective Synthesis of Alcohols, XXXVIII. - Stereoselective Total Synthesis of the Denticulatins

The total synthesis of the denticulatins 1 is described.Key feature is the efficient generation of the C-1-to-C-9 building block 37 by three consecutive stereoselective carbon-carbon bond-forming steps using chiral allylboronates.The C10-to-C-17 building block was obtained by kinetic Sharpless resolution of an allylic alcohol followed by an Ireland-Claisen rearrangement. Key Words: Marine natural products / Hemiketal formation, selective / Denticulatins