172546-41-7

Upstream product

• 172721-76-5 ((1R,4S)-3-Methyl-bicyclo[2.2.1]hept-2-en-2-yl)-methanol 
• 172721-77-6 ((1S,2R,4R)-2-Methyl-3-methylene-bicyclo[2.2.1]hept-2-yl)-acetaldehyde 
• 172721-75-4 (1R,4S)-3-Methyl-bicyclo[2.2.1]hept-2-ene-2-carboxylic acid methyl ester 
• 172546-39-3 (1R,4S)-3-(Diphenoxy-phosphoryloxy)-bicyclo[2.2.1]hept-2-ene-2-carboxylic acid methyl ester 
• 172546-40-6 (1R,4S)-2-(2-Benzenesulfinyl-ethoxymethyl)-3-methyl-bicyclo[2.2.1]hept-2-ene 
• 172721-74-3 (1R,2R,4S)-3-Oxo-bicyclo[2.2.1]heptane-2-carboxylic acid methyl ester 
• 98-59-9 p-toluenesulfonyl chloride 
• 172721-78-7 2-((1S,2R,4R)-2-Methyl-3-methylene-bicyclo[2.2.1]hept-2-yl)-ethanol 

Downstream Products

• 511-59-1 (1S,2R,4R)-2-Methyl-3-methylene-2-(4-methyl-pent-3-enyl)-bicyclo[2.2.1]heptane 

Relevant academic research and scientific papers

Diastereo- and enantio-controlled synthesis of sandalwood constituents (-)-β-santalene and (+)-epi-β-santalene starting from the same (+)-norcamphor

(-)-β-Santalene and (+)-epi-β-santalene, both occurring in East Indian sandalwood oil and having an enantiomeric core bicyclo[2.2.1]heptane framework, have been synthesized in diastereo- and enantio-controlled manner starting from the same (+)-norcamphor.