73346-98-2

Upstream product

• 131846-18-9 1S,2R,3R,5S,4'S,5'S-2-bromo-3-hydroxy-4',5'-bis(benzyloxymethyl)bicyclo<3.2.0>heptane-6-spiro-2'-(1',3'-dioxolane) 

Downstream Products

• 131846-18-9 1R,2S,3S,5R,4'S,5'S-2-bromo-3-hydroxy-4',5'-bis(benzyloxymethyl)bicyclo<3.2.0>heptane-6-spiro-2'-(1',3'-dioxolane) 
• 131846-18-9 1S,2R,3R,5S,4'S,5'S-2-bromo-3-hydroxy-4',5'-bis(benzyloxymethyl)bicyclo<3.2.0>heptane-6-spiro-2'-(1',3'-dioxolane) 
• 1357495-82-9 benzyl 2-(6-oxo-2,4,5,6-tetrahydrocyclopenta[c]pyrrol-4-yl)-acetate 
• 68372-66-7 1β,5β,7α,-7-hydroxy-2-oxabicyclo<3.3.0>octan-3-one 
• 158604-58-1 benzyl 2-(4-oxocyclopent-2-en-1-yl)acetate 
• 132665-10-2 (E)-(R)-4-(tert-Butyl-diphenyl-silanyloxy)-4-((R)-4-oxo-cyclopent-2-enyl)-but-2-enoic acid (E)-(S)-6-iodo-1-methyl-hex-5-enyl ester 
• 20350-15-6 (+)-brefeldin A 
• 84173-27-3 2α,4α-Dihydroxy-cyclopentan-1α-essigsaeure-γ-lacton 

Relevant academic research and scientific papers

OPTICALLY ACTIVE SYNTHONS FOR THE SYNTHESIS OF PROSTANOIDS I. SEPARATION OF THE ENANTIOMERS OF 2-EXO-BROMO-3-ENDO-HYDROXYBICYCLOHEPTAN-6-ONE

Racemic 2-exo-bromo-3-endo-hydroxybicycloheptan-6-one, which is an intermediate for the synthesis of prostanoids, was separated into the enantiomers in the form of the diastereomeric acetals of (S,S)-(-)-1,4-bis(benzyloxy)-2,3-butanediol (the tartaric acid derivative)