300654-95-9

Upstream product

• 21087-29-6 trans-3-phenylprop-2-enyl chloride 
• 300654-91-5 (1R,4S)-3-[1-(2-Hydroxy-phenyl)-meth-(E)-ylidene]-1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-one 
• 464-49-3 (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one 
• 89-95-2 2-methyl-benzyl alcohol 

Relevant academic research and scientific papers

Synthesis of bornene ring-fused dihydrothiopyrans, a new class of chiral cyclic sulfides, via intra-molecular hetero Diels-Alder reaction of homochiral thiabutadienes, 3-(arylmethylene)thiocamphors

A highly diastereoisoface-selective intramolecular hetero Diels-Alder reaction of homochiral camphor-derived thiabutadienes to afford novel, optically active bornene ring-fused dihydrothiopyrans is described for the first time.