141849-08-3

Upstream product

• 141849-07-2 bis<2-(trimethylsilyl)ethyl> cis-5,6-dihydroxy-1,3-cyclohexadiene-2,3-dicarboxylate O-acetonide 
• 2916-68-9 2-(Trimethylsilyl)ethanol 
• 75940-35-1 fumaric acid bis<2-(trimethylsilyl)ethyl>ester 
• 141849-03-8 bis<2-(trimethylsilyl)ethyl> (2-exo,3-endo)-7-oxabicyclo<2.2.1>hept-5-ene-2,3-dicarboxylate 
• 141849-04-9 bis<2-(trimethylsilyl)ethyl> (2-exo,3-endo,5-exo,6-exo)-5,6-dihydroxy-7-oxabicyclo<2.2.1>heptane-2,3-dicarboxylate 
• 141849-05-0 bis<2-(trimethylsilyl)ethyl> (2-exo,3-endo,5-exo,6-exo)-5,6-dihydroxy-7-oxabicyclo<2.2.1>heptane-2,3-dicarboxylate acetonide 
• 141849-06-1 (+/-)-bis<2-(trimethylsilyl)ethyl> 3β,4β,5β-trihydroxy-1-cyclohexene-1,6-dicarboxylate 3,4-O-acetonide 

Downstream Products

• 130073-64-2 phthalic acid cis-4,5-dihydrodiol 

Relevant academic research and scientific papers

The Stereocontrolled Synthesis of Phthalic Acid 4,5-cis-Dihydrodiol. Ab Unambiguous Structural Assignment of the Bacterial Metabolite of Phthalic Acid

The stereocontrolled synthesis of the extremely labile phthalic acid 4,5-cis-dihydrodiol (1) has been achieved in a highly efficient manner in seven steps from bis fumarate (2).The Diels-Alder adduct 3 of the fumarate with furan h