129251-00-9

Upstream product

• 129250-99-3 dimethyl (3R,5R,6S,7S,8R)-6,8-isopropylidenedioxy-7-methoxy-5-<2-(4-methoxybenzyloxy)ethyl>-3-methyl-2-oxo-10-undecenylphosphonate 

Downstream Products

• 129251-01-0 4-formyl-1(R)-methyl-3(E)-butenyl (3R,4S,5S,6R,8R)-10-dimethoxyphosphono-3,5-isopropylidenedioxy-4-methoxy-6-<2-(4-methoxybenzyloxy)ethyl>-8-methyl-9-oxodecanoate 
• 124781-20-0 6-dihydro-6-O-(4-methoxybenzyl)-3,5-O-isopropylideneniddanolide 
• 133839-48-2 niddanolide 4-β-methoxybenzylacetal 
• 133839-48-2 niddanolide 4-α-methoxybenzylacetal 
• 124781-34-6 platenolide W1 4-β-methoxybenzylacetal 
• 124781-34-6 platenolide W1 4-α-methoxybenzylacetal 
• 124781-16-4 carbonolide B 4-β-methoxybenzylacetal 
• 124781-16-4 carbonolide B 4-α-methoxybenzylacetal 
• 124781-17-5 carbonolide A β-4-methoxybenzylacetal 
• 124781-17-5 carbonolide A α-4-methoxybenzylacetal 
• 133839-49-3 EOP aglycon 4-methoxybenzylacetal 
• 124781-16-4 carbonolide B 4-methoxybenzylacetal 
• 124781-34-6 platenolide W₁ 4-methoxybenzylacetal 
• 133839-48-2 niddanolide 4-methoxybenzylacetal 

Relevant academic research and scientific papers

A STEREOCONTROLLED SYNTHESIS OF THE 16-MEMBERED RING MACROLIDE AGLYCONES, NIDDANOLIDE, CARBONOLIDE B, AND PLATENONOLIDE W1

The aglycones of the 16-membered ring macrolide antibiotics, niddanolide, carbonolide B, and platenonolide W1, were synthesized via the Yamaguchi esterification of the C1-C10 segment and the C11-C15 segment, prepared stereoselectively from D-gl