936819-03-3

Upstream product

• 93553-66-3 (2R)-1-(benzyloxy)but-3-en-2-ol 
• 100-39-0 benzyl bromide 
• 936819-01-1 C₃₁H₃₆O₅ 
• 936819-00-0 3-(1-benzyloxymethyl-allyloxy)-1-(4-methoxy-benzyloxy)-pent-4-en-2-ol 
• 780789-09-5 2-(4-methoxy-benzyloxymethyl)-3-vinyl-oxirane 
• 936819-02-2 2-[1-benzyloxy-2-(4-methoxy-benzyloxy)-ethyl]-5-benzyloxymethyl-2,5-dihydro-furan 

Downstream Products

• 936818-99-4 2-benzyloxy-2-(5-benzyloxymethyl-tetrahydro-furan-2-yl)-ethanol 
• 1026476-14-1 benzyloxy-(5-benzyloxymethyl-tetrahydro-furan-2-yl)-acetaldehyde 
• 1028267-09-5 6-benzyloxy-6-(5-benzyloxymethyl-tetrahydro-furan-2-yl)-2-methyl-hexa-2,4-dienal 
• 936819-05-5 6-benzyloxy-6-(5-benzyloxymethyl-tetrahydro-furan-2-yl)-2-methyl-hexa-2,4-dien-1-ol 
• 936819-04-4 6-benzyloxy-6-(5-benzyloxymethyl-tetrahydro-furan-2-yl)-2-methyl-hexa-2,4-dienoic acid ethyl ester 
• 1027023-55-7 8-benzyloxy-8-(5-benzyloxymethyl-tetrahydro-furan-2-yl)-2-butyl-4-methyl-octa-1,4,6-trien-3-ol 

Relevant academic research and scientific papers

Synthesis of the C19-C34 segment of amphidinolide C

The synthesis of the C19-C34 segment of amphidinolide C is described. The key steps include the Mioskowski's Lewis acid catalyzed epoxide opening with the alcohol, ring-closing metathesis, Wittig reaction, and Nozaki-Hiyama-Kishi coupling reaction. Georg