129337-24-2

Upstream product

• 136066-62-1 (+/-)-3-<2-hydroxy-2-methyl-2-(2,4,6-trimethylphenyl)acetoxy>-endo-tricyclo<4.2.1.0^2,5>non-7-ene 
• 136066-61-0 3-(2-oxopropionoxy)-endo-tricyclo<4.2.1.0^2,5>non-7-ene 
• 2633-66-1 2-mesitylmagnesium bromide 

Downstream Products

• 129363-16-2 (S)-2-Hydroxy-2-(2,4,6-trimethyl-phenyl)-propionic acid (3aS,4R,7aS)-2-ethyl-1,3-dioxo-2,3,3a,4,7,7a-hexahydro-1H-isoindol-4-yl ester 
• 129363-16-2 (S)-2-Hydroxy-2-(2,4,6-trimethyl-phenyl)-propionic acid (3aR,4S,7aR)-2-ethyl-1,3-dioxo-2,3,3a,4,7,7a-hexahydro-1H-isoindol-4-yl ester 
• 129337-33-3 (R)-2-Hydroxy-2-(2,4,6-trimethyl-phenyl)-propionic acid (S)-5,5,6,6-tetracyano-cyclohex-2-enyl ester 
• 129337-33-3 (S)-2-Hydroxy-2-(2,4,6-trimethyl-phenyl)-propionic acid (S)-5,5,6,6-tetracyano-cyclohex-2-enyl ester 
• 129337-29-7 (S)-2-Hydroxy-2-(2,4,6-trimethyl-phenyl)-propionic acid (1R,4aS,8aS)-5,8-dioxo-1,4,4a,5,8,8a-hexahydro-naphthalen-1-yl ester 
• 129337-29-7 (S)-2-Hydroxy-2-(2,4,6-trimethyl-phenyl)-propionic acid (1S,4aR,8aR)-5,8-dioxo-1,4,4a,5,8,8a-hexahydro-naphthalen-1-yl ester 
• 129337-31-1 (S)-2-Hydroxy-2-(2,4,6-trimethyl-phenyl)-propionic acid (1R,4aS,9aS)-9,10-dioxo-1,4,4a,9,9a,10-hexahydro-anthracen-1-yl ester 
• 129337-31-1 (S)-2-Hydroxy-2-(2,4,6-trimethyl-phenyl)-propionic acid (1S,4aR,9aR)-9,10-dioxo-1,4,4a,9,9a,10-hexahydro-anthracen-1-yl ester 
• 129337-27-5 (S)-2-Hydroxy-2-(2,4,6-trimethyl-phenyl)-propionic acid (3aS,4R,7aS)-1,3-dioxo-1,3,3a,4,7,7a-hexahydro-isobenzofuran-4-yl ester 
• 129337-27-5 (S)-2-Hydroxy-2-(2,4,6-trimethyl-phenyl)-propionic acid (3aR,4S,7aR)-1,3-dioxo-1,3,3a,4,7,7a-hexahydro-isobenzofuran-4-yl ester 

Relevant academic research and scientific papers

Diene-dienophile hydrogen-bonding control of diels-alder reactions with dienes bearing a remote stereogenic center. Amplification of the receptor nature of dienes by conformational tuning leading to high diastereofacial discrimination

The Diels-Alder reactions of 1-(O-methylmandeloxy)butadiene and its analogues, bearing a remote stereogenic center, have been studied to elucidate the stereoselective control elements. Several model dienes (5a-5f) have been designed to enhance the facial