81177-19-7

Upstream product

• 56-23-5 tetrachloromethane 
• 92419-65-3 Maleinsaeure-mono-(1'R,3'R,4'S)-3-menthylester 
• 627-63-4 fumaryl dichloride 
• 2216-51-5 (-)-menthol 
• 34212-60-7 di-<(1R,2S,5R)-(-)-menthyl>maleate 
• 34675-24-6 di-L-menthyl fumarate 

Downstream Products

• 77341-67-4 L-menthylsuccinic acid 
• 116440-62-1 (E)-But-2-enedioic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester (R)-methoxycarbonyl-phenyl-methyl ester 
• 116415-19-1 (-)-menthyl (-)-phenethyl fumarate 
• 116440-64-3 (1S,2S,3S,4R)-3-Benzyloxycarbonylamino-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester 
• 116440-64-3 (1S,2R,3S,4R)-3-Benzyloxycarbonylamino-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester 
• 116440-67-6 (1S,2S)-4,5-Dimethyl-cyclohex-4-ene-1,2-dicarboxylic acid 1-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl) ester 2-((R)-methoxycarbonyl-phenyl-methyl) ester 
• 116415-21-5 (1R,2S,3S,4S)-3-(Toluene-4-sulfonylamino)-bicyclo[2.2.1]heptane-2-carboxylic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester 
• 116440-65-4 (1S,2S)-4,5-Dimethyl-cyclohex-4-ene-1,2-dicarboxylic acid 1-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl) ester 2-((S)-1-phenyl-ethyl) ester 
• 116440-63-2 (2S,3S)-Bicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid mono-((1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl) ester 

Relevant academic research and scientific papers

IMPROVEMENTS IN OR RELATED TO ORGANIC COMPOUNDS

Malodour counteracting preparations for oral use comprising esterified fumarates of the formula (I) wherein X and Y have the same meaning as given in the description, is disclosed. Furthermore, the invention refers to a process for their preparation and t

Diastereoselectivities in the Diels-Alder reactions of cyclopentadiene with optically active dimenthyl fumarate and menthyl methyl fumarate in LiClO4/ether and on Al2O3

Reactions of cyclopentadiene with (-)-dimenthyl fumarate, which yield adducts 1 and 2, and with (-)-menthyl methyl fumarate, which yield adducts 3 through 6, were carried out on alumina activated at different temperatures, in LiClO4/ether solut

ASYMMETRIC DIELS-ALDER REACTION. A FACILE ROUTE TO CHIRAL ALKYL HYDROGEN CYCLOHEXENE-1,2-DICARBOXYLATE

An efficient route to optically active alkyl hydrogen cyclohexene-1,2-dicarboxylate derivatives by means of asymmetric Diels-Alder reaction of rationally modified chiral fumarates is described.