944798-21-4

Upstream product

• 943226-55-9 C₁₄H₂₆O₄Si 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 188783-40-6 α/β‐L‐glucopyranosyl‐1,2,3,4,5‐pentaacetate 
• 943226-50-4 7,8-bis-benzyloxy-2,2-di-tert-butyl-6-phenylsulfanyl-hexahydro-1,3,5-trioxa-2-silanaphthalene 
• 943226-53-7 C₂₀H₃₂O₅SSi 
• 943226-52-6 C₁₂H₁₆O₅S 
• 943226-48-0 acetic acid 3,4,5-triacetoxy-6-phrnylsulfanyl-tetrahydropyran-2-ylmethyl ester 

Downstream Products

• 943226-54-8 (8R,8aR)-2,2-di-tert-butyl-8-(tert-butyl-diphenyl-silanyloxy)-6-methyl-4,4a,8,8a-tetrahydro-1,3,5-trioxa-2-sila-naphthalene 
• 943226-56-0 (4aS,6R,7S,8R,8aS)-2,2-di-tert-butyl-8-(tert-butyl-diphenyl-silanyloxy)-6-methyl-6-(2-methylallyl)-hexahydro-1,3,5-trioxa-2-sila-naphthalen-7-ol 
• 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-