478309-02-3

Upstream product

• 100-39-0 benzyl bromide 
• 94424-88-1 (2R,3R)-3-(ethyloxiran-2-yl)methanol 

Downstream Products

• 478309-09-0 2-((4R,5R)-5-Benzyloxy-4-ethyl-dec-9-enyl)-4,5,6,7-tetrachloro-isoindole-1,3-dione 
• 1027297-75-1 (R)-2-Ethyl-pent-4-enoic acid ((4R,5R)-5-benzyloxy-4-ethyl-dec-9-enyl)-amide 
• 478309-12-5 (E)-(3R,10R,11R)-10-Benzyloxy-3,11-diethyl-azacyclotetradec-5-en-2-one 
• 478309-07-8 1-((4R,5R)-5-Benzyloxy-4-ethyl-dec-9-enyloxy)-4-methoxy-benzene 
• 478309-06-7 (4R,5R)-4-Ethyl-1-(4-methoxy-phenoxy)-dec-9-en-5-ol 
• 478309-10-3 (4R,5R)-5-Benzyloxy-4-ethyl-dec-9-enylamine 
• 478309-08-9 (4R,5R)-5-Benzyloxy-4-ethyl-dec-9-en-1-ol 
• 478309-04-5 (2S,3R)-3-Ethyl-6-(4-methoxy-phenoxy)-hexane-1,2-diol 
• 478309-05-6 (S)-2-[(R)-1-Ethyl-4-(4-methoxy-phenoxy)-butyl]-oxirane 
• 478309-03-4 (2S,3R)-1-Benzyloxy-3-ethyl-6-(4-methoxy-phenoxy)-hex-4-yn-2-ol 

Relevant academic research and scientific papers

Enantioselective synthesis of 6-nor-fluvirucinin B1

An enantioselective synthesis of the 6-nor-derivative 3 of the antiviral macrocyclic lactam fluvirucinin B1 (2) is presented. Key steps are two regioselective ring opening reactions of chiral epoxides, and a ring-closing metathesis with Grubbs'