173613-41-7

Upstream product

• 173613-36-0 (4aR,5aS,9R,10aS,11R,11aR,3'S)-11-(p-bromobenzoyloxy)-9-((E)-3',4'-di(p-bromobenzoyloxy)-1'-butenyl)-4,4a,5a,6,9,10a,11,11a-octahydro-oxepino[2',3':5,6]pyrano[3,2-d]-1,3-dioxin 
• 188050-75-1 C₃₉H₄₀Br₂O₁₀ 
• 188050-73-9 4-Bromo-benzoic acid (4aR,5aS,8R,9S,10aS,11R,11aR)-9-(tert-butyl-dimethyl-silanyloxymethyl)-8-methanesulfonyloxy-2,2-dimethyl-decahydro-1,3,5,10-tetraoxa-cyclohepta[b]naphthalen-11-yl ester 
• 188050-76-2 C₃₁H₃₂Br₂O₉ 
• 188050-74-0 4-Bromo-benzoic acid (4aR,5aS,9R,10aS,11R,11aR)-9-[(E)-3-hydroxy-4-(4-methoxy-benzyloxy)-but-1-enyl]-2,2-dimethyl-4,4a,5a,6,9,10a,11,11a-octahydro-1,3,5,10-tetraoxa-cyclohepta[b]naphthalen-11-yl ester 
• 173613-33-7 4-Bromo-benzoic acid (4aR,5aS,8R,9S,10aS,11R,11aR)-9-(tert-butyl-dimethyl-silanyloxymethyl)-8-hydroxy-2,2-dimethyl-decahydro-1,3,5,10-tetraoxa-cyclohepta[b]naphthalen-11-yl ester 
• 173613-48-4 4-Bromo-benzoic acid (4aR,5aS,9R,10aS,11R,11aR)-9-(tert-butyl-dimethyl-silanyloxymethyl)-2,2-dimethyl-4,4a,5a,6,9,10a,11,11a-octahydro-1,3,5,10-tetraoxa-cyclohepta[b]naphthalen-11-yl ester 
• 173613-47-3 4-Bromo-benzoic acid (4aR,5aS,8R,9S,10aS,11R,11aR)-8-hydroxy-9-hydroxymethyl-2,2-dimethyl-decahydro-1,3,5,10-tetraoxa-cyclohepta[b]naphthalen-11-yl ester 
• 173613-32-6 4-Bromo-benzoic acid (4aR,5aS,8R,9S,10aS,11R,11aR)-8-hydroxy-2,2-dimethyl-9-vinyl-decahydro-1,3,5,10-tetraoxa-cyclohepta[b]naphthalen-11-yl ester 
• 173613-34-8 4-Bromo-benzoic acid (4aR,5aS,9R,10aS,11R,11aR)-9-hydroxymethyl-2,2-dimethyl-4,4a,5a,6,9,10a,11,11a-octahydro-1,3,5,10-tetraoxa-cyclohepta[b]naphthalen-11-yl ester 
• 3587-60-8 Benzyloxymethyl chloride 
• 173613-37-1 (E)-(S)-4-((4aR,5aS,9R,10aR,11R,11aS)-11-Hydroxy-2,2-dimethyl-4,4a,5a,6,9,10a,11,11a-octahydro-1,3,5,10-tetraoxa-cyclohepta[b]naphthalen-9-yl)-but-3-ene-1,2-diol 

Downstream Products

• 188050-78-4 (S)-2,3-Bis-benzyloxymethoxy-propan-1-ol 

Relevant academic research and scientific papers

Synthetic study of ciguatoxin. Absolute configuration of the C2 hydroxy group

The absolute stereochemistry of the secondary alcohol of the 1,2-dihydroxybutenyl substituent of ciguatoxin (1) was shown to be S by comparing (he split CD curve of ciguatoxin tetra-p-bromobenzoate (2) with those of di- and tri-p-bromobenzoates of AB ring fragments that were synthesized enaotioselectively.