26549-63-3

Upstream product

• 2409-87-2 methyl (2E)-penta-2,4-dienoate 
• 67-56-1 methanol 
• 1515-19-1 cis-cyclohexa-3,5-diene-1,2-dicarboxylic anhydride 
• 5675-13-8 trans-cyclohexa-3,5-diene-1,2-dicarboxylic acid 
• 186581-53-3 diazomethane 
• 26554-23-4 1,3-Cyclohexadien-r-5,c-6-dicarbonsaeure 
• 108-24-7 acetic anhydride 

Downstream Products

• 19926-49-9 2-phenylbenzoic acid ethyl ester 
• 84-66-2 Diethyl phthalate 
• 65-85-0 benzoic acid 
• 51698-72-7 C₂₄H₂₆O₆S₂ 
• 131-11-3 phthalic acid dimethyl ester 
• 77803-95-3 r-1-Acetamido-c-2,c-3,c-4-trisacetoxycyclohexan-t-5,t-6-dicarbonsaeure-dimethylester 
• 77803-95-3 r-1-Acetamido-t-2,t-3,c-4-triacetoxy-t-5,t-6-dicarbonsaeure-dimethylester 
• 77803-95-3 r-1-Acetamido-c-2,t-3,c-4-trisacetoxycyclohexan-t-5,t-6-dicarbonsaeure-dimethylester 
• 77803-97-5 r-1-Acetamido-c-2,c-4-diacetoxy-t-3-bromcyclohexan-t-5,t-6-dicarbonsaeure-dimethylester 
• 77803-93-1 r-1-Acetamido-c-4-acetoxy-2-cyclohexen-t-5,t-6-dicarbonsaeure-dimethylester 
• 118215-79-5 (1R,2S,3S,4S,7R,8R)-7,8-Bis-benzenesulfonyl-bicyclo[2.2.2]oct-5-ene-2,3-dicarboxylic acid dimethyl ester 
• 118215-79-5 (1S,2R,3R,4R,7R,8S)-7,8-Bis-benzenesulfonyl-bicyclo[2.2.2]oct-5-ene-2,3-dicarboxylic acid dimethyl ester 

Relevant academic research and scientific papers

Synthese de phosphinites derives de sucres: applications en cyclodimerisation du penta 2,4-dienoate de methyle, en hydrogenation et en hydrosilylation de la pentolactone

Sugar-derived phosphinites, when used as ligands in the catalytic hydrogenation of α-ketopentolactone, lead to the corresponding alcohol with a better enantiomeric excess (20percent) than in hydrosilylation (10percent).In the cyclodimerisation of penta-2,4-dienoic acid methyl ester they lead to the meso cycloocta-3,7-diene-1,2-doic dimethyl ester.

Organometallic Compounds in Organic Synthesis. Part 13. Stereoselectivity of Complexation of Cyclohexadiene Esters

Complexation of cyclohexadienes with Fe(CO)3 as the entering group are subject to classical steric hindrance by alkyl groups, but CO2R and related groups introduce a competing factor because they favour sterically the entering group, probably through an i

Polyhydroxyamino Compounds via Diene Synthesis with Nitroso Compounds, V. 1,3-Cyclohexadiene-5,6-dicarboxylic Acid Derivatives as Reactants

The use of 1,3-cyclohexadiene-5,6-dicarboxylic acid derivatives as educts for the reaction sequence: Diels-Alder reaction with nitroso compounds, reduction of the adducts, hydroxylation, gives hexa-substituted cyclohexanes.However, attempts to synthesize