178686-32-3

Upstream product

• 178686-41-4 2-O-allyl-1,3-di-O-benzyl-2-C-methyl-D-ribitol 
• 35784-67-9 1,2;5,6-di-O-isopropylidene-3-C-methyl-α-D-allofuranose 
• 156742-39-1 3-O-allyl-1,2-O-isopropylidene-3-C-methyl-α-D-allofuranose 
• 174019-53-5 3-O-allyl-1,2:5,6-di-O-isopropylidene-3-C-methyl-α-D-allofuranose 
• 178686-38-9 2-O-allyl-2-C-methyl-D-ribitol 
• 178686-36-7 (R)-4-((1R,2S)-2-Allyloxy-1,3-dihydroxy-2-methyl-propyl)-[1,3]dioxolan-2-one 
• 178686-39-0 4-O-allyl-1,2-O-isopropylidene-4-C-methyl-L-ribitol 
• 178686-35-6 Formic acid (1R,2R)-2-allyloxy-2-methyl-3-oxo-1-((R)-2-oxo-[1,3]dioxolan-4-yl)-propyl ester 
• 178686-33-4 (R)-4-((3aR,5R,6R,6aR)-6-Allyloxy-2,2,6-trimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-[1,3]dioxolan-2-one 
• 178686-40-3 4-O-allyl-3,5-di-O-benzyl-1,2-O-isopropylidene-4-C-methyl-L-ribitol 

Relevant academic research and scientific papers

Synthetic studies on zoapatanol: Construction of oxepanes via an intramolecular 1,3-dipolar cycloaddition strategy

The nitrones derived from β-allyloxyaldehydes with a β-quaternary centre cyclized to give six- instead of seven-membered O-heterocycles exclusively whereas a nitrile oxide derived from a γ-allyloxyaldehyde with a γ-quaternary centre cyclized to yield an o