164327-62-2

Upstream product

• 164327-44-0 (R)-4-((R)-Allyloxy-phenyl-methyl)-2,2-dimethyl-[1,3]dioxolane 
• 100-59-4 phenylmagnesium chloride 
• 16354-89-5 (R)-[(R)-2,2-dimethyl-1,3-dioxolan-4-yl](phenyl)methanol 
• 164327-52-0 (E)-4-[(R)-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-phenyl-methoxy]-but-2-enoic acid methyl ester 

Relevant academic research and scientific papers

Comparison of Stereoselectivity of Intramolecular Cyclization of Aldehydes Tethered with Conjugated Esters Induced by O-Stannyl and O-Samarium Ketyls to Form the Tetrahydrofuran Ring Systems

Several (E)- and (Z)-ω-formyl-5-oxa-2-substituted-α,β-unsaturated esters (6Za-6Zc; 6Ea-6Ec; 6Eb'-6Ec'; 6Zb'-6Zc') were prepared in high yields.They were subjected to cyclization of their intramolecular ketyl radicals induced by either samarium(II) iodide