1146690-71-2

Upstream product

• 1146690-70-1 (2S)-2-[6-(benzyloxy)hexyl]-5-ethoxy-3-methyltetrahydrofuran 
• 1146690-65-4 ethyl (E)-9-(benzyloxy)-2-nonenoate 
• 1146690-85-8 (E)-9-(benzyloxy)-2-nonen-1-ol 
• 1146690-66-5 {(2S,3S)-3-[6-(benzyloxy)hexyl]oxiran-2-yl}methanol 
• 1146690-86-9 (2S,3R)-2-[6-(benzyloxy)hexyl]-3-(chloromethyl)oxirane 
• 1146690-67-6 (3S)-9-(benzyloxy)-1-nonyn-3-ol 
• 141943-06-8 1,7-heptanediol monobenzyl ether 
• 129649-05-4 7-benzyloxyheptan-1-ol 
• 1146690-68-7 (2S)-2-[6-(benzyloxy)hexyl]-5-ethoxy-3-methylenetetrahydrofuran 
• 1146690-87-0 (3S)-9-(benzyloxy)-3-(2-bromo-1-ethoxyethoxy)-1-nonyne 

Downstream Products

• 1146690-72-3 (4S,5S)-5-[6-(benzyloxy)hexyl]-4-methyltetrahydro-2-furanol 
• 1146690-75-6 (4S)-3-{6-[(2S,3S,5S)-5-allyl-3-methyl-tetrahydrofuran-2-yl]hexanoyl}-4-benzyl-1,3-oxazolan-2-one 
• 1146690-90-5 (4S)-3-((2S)-6-[(2S,3S,5S)-5-allyl-3-methyltetrahydro-2-furanyl]-2-methylhexanoyl)-4-benzyl-1,3-oxazolan-2-one 
• 1269803-16-8 ((S)-6-{(2S,3S,5R)-5-[2-(4-methoxybenzyloxy)ethyl]-3-methyltetrahydrofuran-2-yl}-2-methylhexyloxy)(tert-butyl)dimethylsilane 
• 1269803-28-2 (S)-6-{(2S,3S,5R)-5-[2-(4-methoxybenzyloxy)ethyl]-3-methyltetrahydrofuran-2-yl}-2-methylhexan-1-ol 
• 1269803-20-4 (S)-((4R,8R)-9-(benzyloxy)-8-methyl-6-methylenenonan-4-yl)-6-((2S,3S,5R)-5-(2-(4-methoxybenzyloxy)ethyl)-3-methyltetrahydrofuran-2-yl)-2-methylhexanoate 
• 1269803-11-3 (S)-6-{(2S,3S,5R)-5-[2-(4-methoxybenzyloxy)ethyl]-3-methyltetrahydrofuran-2-yl}-2-methylhexanoic acid 

Relevant academic research and scientific papers

First stereoselective total synthesis and biological evaluation of amphidinin B and Its analogues

A highly stereoselective first total synthesis of amphidinin B is described. The key steps involved in this synthesis are the generation of the exo-double bond in the C1-C9 segment, the Barbier allylation, enzymatic kinetic resolutio

Stereoselective synthesis of amphidinolide T1

A highly stereoselective total synthesis of amphidinolide T1 is achieved using Sharpless asymmetric epoxidation, base-induced epoxide opening, radical cyclization, diastereoselective reduction followed by allylation, Evans methylation, base-induced reduct