89919-54-0

Basic information

• Product Name: ethyl (+)-(R)_s-(1R,4S)-endo-2-methyl-exo-3-(p-tolylsulfinyl)bicyclo<2.2.1>hept-5-ene-exo-2-carboxylate
• Synonyms: ethyl (+)-(R)_s-(1R,4S)-endo-2-methyl-exo-3-(p-tolylsulfinyl)bicyclo<2.2.1>hept-5-ene-exo-2-carboxylate
• CAS NO: 89919-54-0
• Molecular Weight: 318.437
• Mol File: 89919-54-0.mol

Chemical Properties

• CAS DataBase Reference: ethyl (+)-(R)_s-(1R,4S)-endo-2-methyl-exo-3-(p-tolylsulfinyl)bicyclo<2.2.1>hept-5-ene-exo-2-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl (+)-(R)_s-(1R,4S)-endo-2-methyl-exo-3-(p-tolylsulfinyl)bicyclo<2.2.1>hept-5-ene-exo-2-carboxylate(89919-54-0)
• EPA Substance Registry System: ethyl (+)-(R)_s-(1R,4S)-endo-2-methyl-exo-3-(p-tolylsulfinyl)bicyclo<2.2.1>hept-5-ene-exo-2-carboxylate(89919-54-0)

Safety Data

• Hazardous Substances Data: 89919-54-0(Hazardous Substances Data)

Upstream product

• 269719-23-5 diethyl p-tolylsulfinylmethylphosphonate 
• 617-35-6 2-oxo-propionic acid ethyl ester 
• 89764-37-4 ethyl (-)-(Z)-(R)_s-2-methyl-3-(p-tolylsulfinyl)propenoate 
• 542-92-7 cyclopenta-1,3-diene 

Downstream Products

• 89826-18-6 ethyl (+)-(1S,4R)-endo-2-methyl-3-(p-tolylthio)bicyclo<2.2.1>heptane-exo-2-carboxylate 
• 108653-79-8 (-)-(1S,4R)-endo-2-methyl-3-oxobicyclo<2.2.1>heptane-exo-2-carboxaldehyde 
• 89826-17-5 (1S,2S,3S,4R)-2-Methyl-3-((R)-toluene-4-sulfinyl)-bicyclo[2.2.1]heptane-2-carboxylic acid ethyl ester 
• 108692-16-6 ethyl (-)-(1R,4S)-exo-2-methyl-endo-3-(p-tlylthio)bicyclo<2.2.1>heptane-endo-2-carboxylate 

Relevant articles and documents

The Asymmetric Diels-Alder Cycloaddition Using Ethyl(-)-(Z)-(R)s-2-methyl-3-(p-tlylsulfinyl)propenoate: Application to an Enantioselective Synthesis of (+)-epi-β-Santalene

The Diels-Alder reaction of ethyl (-)-(Z)-(R)s-2-methyl-3-(p-tolylsulfinyl)propenoate (6) with cyclopentadiene gave the adducts, 7, 8, and 9 in a high diastereoselective manner.The cycloadduct 7 was transformed into the acetal (-)-25.The racemic 25 was used as an intermediate in the synthesis of (+/-)-β-santalol.Thus, the chiral acetal (-)-25 should provide a route to (-)-Β-santalol.The cycloadduct 8 was converted into (+)-epi-β-santalene in 11 steps.