111555-72-7

Upstream product

• 100-39-0 benzyl bromide 
• 19700-97-1 3,4-dihydroxy-D,L-threo-hexa-1,5-diene 
• 151477-85-9 3,4-di-O-benzyl-1,2:5,6-di-O-sulfenyl-D-mannitol 
• 1707-77-3 1,2:5,6-di-O-isopropylidene-D-mannitol 
• 111476-62-1 3,4-di-O-benzyl-1,2:5,6-di-O-isopropylidene-D-mannitol 
• 722539-36-8 3,4-di-O-benzyl-1,2:5,6-di-O-sulfinyl-D-mannitol 
• 36199-02-7 3,4-di-O-benzyl-D-mannitol 
• 111476-63-2 3,4-dibenzyloxy-1,2,5,6-tetra-O-mesyl-D-mannitol 

Downstream Products

• 101924-27-0 3,4-dibenzyloxy-D,L-threo-hex-5-en-1-ol 
• 129115-89-5 3,4-dibenzyloxy-2,5-dihydroxymethyltetrahydrofuran 
• 300807-58-3 ((2R,3R,4R,5S)-3,4-Bis-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-yl)-methanol 
• 102208-54-8 2,5-anhydro-3,4,6-tri-O-benzyl-D-glucitol 
• 101924-29-2 3,4-dibenzyloxy-D,L-threo-nona-3,8-dien-2-one 
• 101924-28-1 3,4-dibenzyloxy-D,L-threo-hex-5-en-1-al 

Relevant academic research and scientific papers

Applications of Cyclic Sulfates of vic-Diols: Synthesis of Episulfides, Olefins, and Thio Sugars

A new efficient and expeditious one-pot synthesis of thiiranes and olefins from cyclic sulfates of inc-diols is described. Opening of cyclic sulfates with potassium thioacetate or potassium thiocyanate followed by treatment with sodium methoxide led to ep

A Simple Synthesis of R,R-3,4-Dibenzyloxy-threo-hexa-1,5-diene (R,R-Divinylglycol) from D-Mannitol

Synthesis of R,R-divinylglycol (1) from D-mannitol (2) involves (i) conversion of 2 into (1,2:5,6)-di-O-isopropylidene-D-mannitol (3); (ii) benzylation of 3 to the corresponding 3,4-dibenzyloxy derivative (4); (iii) hydrolysis of 4 to a tetrol and its con

A Short Synthesis of d,l-exo-Brevicomin from Divinylglycol

d,l-exo-Brevicomin is obtained from meso-divinylglycol via bis-O-benzylation, selective ω-hydroxylation of one double bond, oxidation of the hydroxymethyl group to the aldehyde stage, chain extension at the aldehyde function by Wittig reaction, and hydrog