502464-35-9

Upstream product

• 556-56-9 allyl iodid 
• 412021-21-7 (4-tert-Butyl-phenyl)-methanesulfonic acid (3aR,5R,6R,6aR)-5-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl ester 

Downstream Products

• 502464-40-6 (3R,5R)-3-(4-tert-butylphenyl)-5-methyl-1,2-oxathiolane 2,2-dioxide 

Relevant academic research and scientific papers

A practical approach towards the asymmetric synthesis of α,γ-substituted γ-sultones

The first auxiliary controlled synthesis of enantiopure α,γ-substituted γ-sultones via α-allylated chiral sulfonates is described. The high asymmetric inductions of the α-allylations were reached with our previously described auxiliary 1,2:5,6-di-O-isopro

Asymmetric Synthesis of α,γ-Substituted γ-Sultones via Allylation of Chiral Lithiated Sulfonates

The first auxiliary controlled asymmetric synthesis of enantiopure α,γ-substituted γ-sultones via α-allylation of lithiated sulfonates by using 1,2:5,6-di-O-isopropylidene-α -D-allofuranose as chiral auxiliary is described. The high asymmetric inductions