324027-27-2

Upstream product

• 23202-83-7 5-benzyl-1,2-O-isopropylidene-α-D-xylofuranose 
• 399534-53-3 Chloro-acetic acid (3R,3aR,6S,6aR)-6-benzyloxy-hexahydro-furo[3,2-b]furan-3-yl ester 
• 111956-66-2 (3R,3aR,6S,6aR)-6-(Benzyloxy)hexahydrofuro[3,2-b]furan-3-ol 
• 20031-21-4 1,2-O-isopropylidene-α-D-xylose 
• 100-39-0 benzyl bromide 
• 352530-47-3 Chloro-acetic acid (3aR,5R,6S,6aR)-5-benzyloxymethyl-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-yl ester 
• 603-35-0 triphenylphosphine 

Relevant academic research and scientific papers

Highly diastereoselective 5-hexenyl radical cyclizations with Lewis acids and carbohydrate scaffolds.

[figure: see text] Carbohydrates as removable chiral scaffolds for free radical cyclizations were examined for the first time. This investigation illustrates the utility of two inexpensive carbohydrate derivatives as sources of asymmetry for 5-hexenyl rad