1543148-52-2

Upstream product

• 1543148-26-0 (3R,6S,7S,E)-ethyl 6-(benzyloxy)-3-ethyl-7,8-dihydroxyoct-4-enoate 
• 1543148-29-3 (3R,6S,7S,E)-ethyl 6-(benzyloxy)-3-ethyl-7-hydroxy-8-(tosyloxy)oct-4-enoate 
• 1543148-32-8 (3R,6S,7S,E)-6-(benzyloxy)-3-ethyloct-4-ene-1,7-diol 
• 1543148-33-9 (2S,3S,6R,E)-3-(benzyloxy)-6-ethyl-8-iodooct-4-en-2-ol 
• 1543148-21-5 (2S,3S,4R,Z)-3-(benzyloxy)oct-5-ene-1,2,4-triol 
• 1543148-35-1 ((2S,3S,6R,E)-6-ethyl-8-iodooct-4-ene-2,3-diyl)bis(oxy)bis(methylene)dibenzene 
• 100-39-0 benzyl bromide 
• 1543148-38-4 (4R,7S,8S,E)-7,8-bis(benzyloxy)-4-ethyl-10-methylundeca-5,9-dienenitrile 
• 1543148-40-8 (4R,7S,8S,E)-7,8-bis(benzyloxy)-4-ethyl-10-methylundeca-5,9-dienal 
• 98760-37-3 (3aR,5R,6S,6aR)-6-(benzyloxy)-5-((Z)-but-1-en-1-yl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxole 
• 23558-05-6 3-O-benzyl-1,2-O-isopropylidene-1,5-D-xylo-dialdofuranose 
• 582-52-5 1,2:5,6-di-O-isopropylidene-α-D-glucofuranose 
• 18685-18-2 3-O-benzyl-1,2-5,6-O-diisopropylidene-α-D-glucofuranose 
• 1543148-25-9 (3R,6S,E)-ethyl 6-(benzyloxy)-6-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)-3-ethylhex-4-enoate 

Relevant academic research and scientific papers

Studies towards the total synthesis of hygrocins A and B

The western segment of hygrocins A-B has been synthesized through the coupling of a chiral C5-C13 synthon with the sterically demanding hexasubstituted naphthalenic core. The C5-C13 chiral fragment has been assembled via a stereoselective Johnson orthoest