115369-24-9

Upstream product

• 100-39-0 benzyl bromide 
• 81096-93-7 (R)-1-O-benzyl-1,2,4-butanetriol 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 862603-72-3 (S)-1-((2S,5R)-5-Benzyloxymethyl-tetrahydro-furan-2-yl)-propane-1,3-diol 
• 862603-18-7 (S)-1-((2S,5R)-5-Benzyloxymethyl-tetrahydro-furan-2-yl)-but-3-en-1-ol 
• 862603-15-4 (2R,5S)-2-Benzyloxymethyl-5-((R)-toluene-4-sulfinylmethyl)-tetrahydro-furan 
• 862603-20-1 Toluene-4-sulfonic acid (S)-3-((2S,5R)-5-benzyloxymethyl-tetrahydro-furan-2-yl)-3-hydroxy-propyl ester 
• 862603-24-5 (2S,5R,2'S,5'R)-5'-Benzyloxymethyl-5-((S)-toluene-4-sulfinylmethyl)-octahydro-[2,2']bifuranyl 
• 862603-22-3 (2R,5S)-2-Benzyloxymethyl-5-{(S)-3-iodo-1-[(E)-2-((S)-toluene-4-sulfinyl)-vinyloxy]-propyl}-tetrahydro-furan 
• 862603-74-5 Toluene-4-sulfonic acid (S)-3-((2S,5R)-5-benzyloxymethyl-tetrahydro-furan-2-yl)-3-[(E)-2-((S)-toluene-4-sulfinyl)-vinyloxy]-propyl ester 
• 862603-81-4 [(S)-1-((2S,5R,2'S,5'R)-5'-Benzyloxymethyl-octahydro-[2,2']bifuranyl-5-yl)-undecyloxy]-tert-butyl-dimethyl-silane 
• 170305-54-1 (2S,5R)-5-<(Benzyloxy)methyl>tetrahydrofuran-2-carboxaldehyde 
• 862603-26-7 (2S,5R,2'S,5'R)-5'-Benzyloxymethyl-octahydro-[2,2']bifuranyl-5-carbaldehyde 
• 158010-33-4 (S)-1-((2S,5R,2'S,5'R)-5'-Benzyloxymethyl-octahydro-[2,2']bifuranyl-5-yl)-undecan-1-ol 
• 115369-26-1 (R)-4-Benzenesulfonyl-1-benzyloxy-butan-2-ol 
• 862603-13-2 Toluene-4-sulfonic acid (R)-4-benzyloxy-3-[(E)-2-((R)-toluene-4-sulfinyl)-vinyloxy]-butyl ester 
• 115369-25-0 (R)-1-Benzyloxy-4-phenylsulfanyl-butan-2-ol 

Relevant academic research and scientific papers

Stereoselective syntheses of rolliniastatin 1, rollimembrin, and membranacin

A radical cyclization of β-alkoxyvinyl sulfoxides-Pummerer rearrangement-allylation protocol was successfully applied to the synthesis of the threol cis/threol cis/erythro bis-oxolane moiety in rolliniastatin 1 (1), rollimembrin (2), and membranacin (3).

SYNTHESIS OF A MARINE POLYETHER TOXIN, OKADAIC ACID (2) -- SYNTHESIS OF SEGMENT B

The central synthetic segment B for okadaic acid comprises the carbons from 15 through 27 including 6 asymmetric carbons.Its synthesis started from a D-glucose derivative, whose carbon was extended twice for the six and five membered etherial ring formati