1357362-60-7

Upstream product

• 283177-05-9 (1'S,3'R,4'R,6'R)-2-[4'-bromo-3',7',7'-trimethylbicyclo(4.1.0)hept-3'-yloxy]ethan-1-ol 
• 17686-89-4 6--chrysen 
• 283177-06-0 (1'S,3'R,4'R,6'R)-2-[4'-bromo-3',7',7'-trimethylbicyclo(4.1.0)hept-3'-yloxy]acetic acid 
• 498-15-7 (+)-Δ³-carene 

Downstream Products

• 1215310-74-9 (3R,4R)-1-(chrysen-6-yl)-3-hydroxy-4-(4-methoxyphenyl)azetidin-2-oneacetate 
• 1215310-72-7 (3R,4R)-1-(chrysen-6-yl)-3-hydroxy-4-phenylazetidin-2-one 

Relevant academic research and scientific papers

An efficient synthesis of optically active trans-(3R,4R)-3-acetoxy-4-aryl- 1-(chrysen-6-yl)azetidin-2-ones using (+)-car-3-ene as a chiral auxiliary

An efficient enantioselective synthesis of 3-acetoxy trans-β-lactams 7a and 7b via [2+2] cycloaddition reactions of imines 4a and 4b, derived from a polycyclic aromatic amine and bicyclic chiral acid obtained from (+)-car-3-ene, is described. The cycloadd