3-O-benzoyl-4,5-dideoxy-1,2-O-isopropylidene-α-L-glycero-hex-4-en-2-ulopyranose

Base Information

Chemical Name:3-O-benzoyl-4,5-dideoxy-1,2-O-isopropylidene-α-L-glycero-hex-4-en-2-ulopyranose
CAS No.:99648-50-7
Molecular Formula:C₁₆H₁₈O₅
Molecular Weight:290.316
Hs Code.:

Synonyms:3-O-benzoyl-4,5-dideoxy-1,2-O-isopropylidene-α-L-glycero-hex-4-en-2-ulopyranose

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Chemical Property of 3-O-benzoyl-4,5-dideoxy-1,2-O-isopropylidene-α-L-glycero-hex-4-en-2-ulopyranose

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Technology Process of 3-O-benzoyl-4,5-dideoxy-1,2-O-isopropylidene-α-L-glycero-hex-4-en-2-ulopyranose

There total 6 articles about 3-O-benzoyl-4,5-dideoxy-1,2-O-isopropylidene-α-L-glycero-hex-4-en-2-ulopyranose which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 87.0%

: 99648-49-4
3-O-benzoyl-1,2-O-isopropylidene-β-D-fructopyranose

: 99648-50-7
3-O-benzoyl-4,5-dideoxy-1,2-O-isopropylidene-α-L-glycero-hex-4-en-2-ulopyranose

Guidance literature:: With 1H-imidazole; iodine; triphenylphosphine; In tetrahydrofuran; for 20h; regioselective reaction; Reflux; Inert atmosphere;
DOI:10.1002/ejoc.201001325

Reference yield: 80.0%

: 99648-48-3
3-O-benzoyl-1,2-O-isopropylidene-4,5-di-O-mesyl-β-D-fructopyranose

: 99648-50-7
3-O-benzoyl-4,5-dideoxy-1,2-O-isopropylidene-α-L-glycero-hex-4-en-2-ulopyranose

Guidance literature:: With copper; potassium iodide; zinc; In N,N-dimethyl-formamide; for 4h; Heating;

Reference yield:

: 7660-25-5
D-fructose

: 99648-50-7
3-O-benzoyl-4,5-dideoxy-1,2-O-isopropylidene-α-L-glycero-hex-4-en-2-ulopyranose

Guidance literature:: Multi-step reaction with 4 steps

1: 53 percent / HClO₄ / acetone / 0 °C

2: 93 percent / Et₃N / CH₂Cl₂ / 20 °C

3: 92 percent / DDQ / acetonitrile; H₂O / 24 h / 20 °C

4: 79 percent / Ph₃P; imidazole; I₂ / Zn / toluene / 3.5 h

With 1H-imidazole; perchloric acid; iodine; triethylamine; triphenylphosphine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; zinc; In dichloromethane; water; acetone; toluene; acetonitrile;
DOI:10.1021/ol000385q