120400-68-2

Upstream product

• 824-94-2 p-methoxybenzyl chloride 
• 18427-19-5 1,2;5,6-di-O-isopropylidene-3-(2-hydroxyethyl)-α-D-allofuranoside 
• 133839-52-8 (3aR,5S,6R,6aR)-5-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-6-[2-(4-methoxy-benzyloxy)-ethyl]-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxole 

Downstream Products

• 133839-45-9 (2R,4R,5S,6S,7R)-6-methoxy-4-<2-(4-methoxybenzyloxy)ethyl>-2-methyl-9-decene-1,5,7-triol 
• 129250-96-0 2(S)-<2(S)-isopropyloxy-5(R)-<2-(4-methoxybenzyloxy)ethyl>-3(R)-methyl-6(S)-tetrahydropyranyl>-2-methoxyethanol 
• 133839-44-8 2(S)-<2(S)-isopropyloxy-5(R)-<2-(4-methoxybenzyloxy)ethyl>-3(R)-methyl-6(S)-tetrahydropyranyl>-2-methoxyethanal 
• 129250-98-2 (2R,4R,5S,6S,7R)-5,7-isopropylidenedioxy-6-methoxy-4-<2-(4-methoxybenzyloxy)ethyl>-2-methyl-9-decenol 
• 133839-53-9 (2S,3R,4S,5S)-5-((S)-2-Benzyloxy-1-methoxy-ethyl)-4-[2-(4-methoxy-benzyloxy)-ethyl]-tetrahydro-furan-2,3-diol 
• 133839-46-0 (2R,4R,5S,6S,7R)-5,7-isopropylidenedioxy-6-methoxy-4-<2-(4-methoxybenzyloxy)ethyl>-2-methyl-9-decenal 
• 129250-93-7 (2R,3R,4S)-5-benzyloxy-3-formyloxy-4-methoxy-2-<2-(4-methoxybenzyloxy)ethyl>pentanal 
• 133850-00-7 6-O-benzyl-3-deoxy-1,2-O-isopropylidene-3-C-<2-(4-methoxybenzyloxy)ethyl>-β-L-talofuranose 
• 133839-42-6 (2Z,4S,5S,6S)-7-benzyloxy-5-hydroxy-6-methoxy-4-<2-(4-methoxybenzyloxy)ethyl>-2-methylhept-2-enoic acid δ-lactone 
• 129250-92-6 6-O-benzyl-3-deoxy-1,2-O-isopropylidene-3-C-<2-(4-methoxybenzyloxy)ethyl>-5-O-methyl-β-L-talofuranose 
• 133839-43-7 (2S,5S,6S)-6-<2-benzyloxy-1(S)-methoxyethyl>-5,6-dihydro-2-isopropyloxy-5-<2-(4-methoxybenzyloxy)ethyl>-3-methylpyran 
• 133839-55-1 [(3R,5R)-5-((4S,5S,6R)-6-Allyl-5-methoxy-2,2-dimethyl-[1,3]dioxan-4-yl)-2-hydroxy-7-(4-methoxy-benzyloxy)-3-methyl-heptyl]-phosphonic acid dimethyl ester 
• 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 
• 129272-57-7 5(S)-<2(S)-isopropyloxy-5(R)-<2-(4-methoxybenzyloxy)ethyl>-3(R)-methyl-6(S)-tetrahydropyranyl>-4(R)-hydroxy-5-methoxypentene 

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