943226-82-2

Upstream product

• 96481-69-5 (2S)-2-methyl-4-(benzyloxy)-1-butanal 
• 943226-83-3 C₁₈H₂₆O₃ 
• 943226-80-0 5-allyl-2-(3-benzyloxy-1-methylpropyl)-3-methyl-tetrahydro-furan 
• 943226-77-5 7-benzyloxy-4-(tert-butyl-dimethyl-silanyloxy)-3,5-dimethyl-heptan-1-ol 
• 1027149-17-2 C₂₁H₃₂O₅ 
• 80522-42-5 triisopropylsilyl trifluoromethanesulfonate 

Downstream Products

• 943226-84-4 4-[5-(3-benzyloxy-1-methylpropyl)-4-methyl-tetrahydro-furan-2-yl]-3-triisopropylsilanyloxy-butyric acid 
• 943226-85-5 4-[5-(3-benzyloxy-1-methylpropyl)-4-methyl-tetrahydro-furan-2-yl]-3-triisopropylsilanyloxy-butyric acid 2-but-3-enyl-10a,11a-dimethyl-dodecahydro-1,5,10-trioxa-cyclohepta[b]naphthalen-3-yl ester 
• 943226-87-7 4-[5-(3-benzyloxy-1-methylpropyl)-4-methyl-tetrahydro-furan-2-yl]-3-triisopropylsilanyloxy-butyric acid 2-but-3-enyl-10a,11a-dimethyl-dodecahydro-1,5,10-trioxa-cyclohepta[b]naphthalen-3-yl ester 

Relevant academic research and scientific papers

Synthesis of an A-E gambieric acid subunit with use of a C-glycoside centered strategy

This paper describes our synthesis of the A-E subunit of gambieric acid (GA) in addition to the synthesis of the A-ring and the C-E tricycle The use of an enol ether-olefin RCM strategy to couple the A and C-E subunits and, in the process, generate the B-