78469-92-8

Upstream product

• 120575-87-3 (R)-2-Benzyloxy-1-((2R,3R)-3-trimethylsilanyl-oxiranyl)-ethanol 
• 119180-87-9 (2S,3E)-1-(benzyloxy)-4-(trimethylsilyl)but-3-en-2-ol 
• 119046-49-0 (E)-1-Benzyloxy-4-trimethylsilanyl-but-3-en-2-ol 
• 60656-87-3 benzyloxyacetoaldehyde 
• 14593-43-2 benzyl allyl ether 
• 78469-79-1 Toluene-4-sulfonic acid (2R,3R)-4-benzyloxy-2,3-dihydroxy-butyl ester 
• 78469-75-7 (2R,3R)-p-nitrobenzoesaeure-(1-benzyloxy-3,4-epoxy-2-butyl)ester 
• 78469-88-2 (2S,3R)-p-nitrobenzoesaeure-(1-benzyloxy-3,4-epoxy-2-butyl)ester 
• 72229-13-1 (2R,3R)-1-benzyloxy-3,4-epoxy-2-butanol 
• 78469-77-9 1-O-benzyl-2,3-O-isopropylidene-D-threitol 
• 100-39-0 benzyl bromide 
• 78469-78-0 (4R,5R)-p-toluolsulfonsaeure<(5-benzyloxymethyl-5-hydroxymethyl-2,2-dimethyl-1,3-dioxolan-4-yl)methyl>ester 
• 116-11-0 2-Methoxypropene 
• 78469-89-3 (2S,3R)-1-benzyloxy-3,4-epoxy-2-butanol 

Downstream Products

• 109784-19-2 (2R,3S)-2-<4-benzyloxy-2,3-(isopropylidenedioxy)butyl>-2-methyl-1,3-dithiane 
• 109784-20-5 (4R,5S)-6-benzyloxy-4,5-isopropylidenedioxy-2-hexanone 

Relevant academic research and scientific papers

A Practical Synthesis of Several Polyhydroxylated Chiral Building Blocks

A practical method for the synthesis of several useful polyhydroxylated chiral building blocks has been developed.The key reaction is the kinetic resolution of (E)-1-trimethylsilyl-4-alkoxy-1-buten-3-ol or (E)-1-trimethylsilyl-5-alkoxy-1-penten-3-ol using the Sharpless asymmetric epoxidation reaction.

Chiral Electrophilic Synthetic Building Blocks with Four Different Functional Groups from Tartaric Acid, 2,3- and 3,4-Epoxy-butanediol Derivatives in All Four Stereoisomeric Forms

Efficient and simple procedures have been developed for the preparation of the threo- and erythro-3,4-epoxy-1,2-butanediol derivatives 7 and 9 in both enantiomeric forms from tartaric acid.These epoxides should prove versatile as alkylating reagents in sy