853911-96-3

Upstream product

• 853911-91-8 (+)-1,1,7-trimethyl-2-(triethylsilyloxy)bicyclo[2.2.1]heptan-2-one 
• 464-49-3 (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one 
• 994-30-9 triethylsilyl chloride 
• 853911-89-4 (+)-(1R,4S)-1,7,7-trimethyl-2-(triethylsilyloxy)bicyclo[2.2.1]hept-2-en 

Downstream Products

• 31503-17-0 (-)-(1R,2R,3R,4S)-1,7,7-trimethyl-2-phenyl-bicyclo[2.2.1]heptane-2,3-diol 

Relevant academic research and scientific papers

Practical and efficient multigram preparation of a camphor-derived diol for the enantioselective Lewis acid catalyzed allylboration of aldehydes

Chiral diols are important molecules with widespread use as chiral auxiliaries and ligands in enantioselective synthesis. Therefore, efficient and practical syntheses of highly dissymmetrical nonracemic diols are still a meaningful pursuit. Two new routes