3,6-anhydro-7-O-benzoyl-5-O-benzyl-2-deoxy-7-C-phenyl-D-glycero-L-ido-heptono-1,4-lactone

Base Information

Chemical Name:3,6-anhydro-7-O-benzoyl-5-O-benzyl-2-deoxy-7-C-phenyl-D-glycero-L-ido-heptono-1,4-lactone
CAS No.:1361026-56-3
Molecular Formula:C₂₇H₂₄O₆
Molecular Weight:444.484
Hs Code.:

Synonyms:3,6-anhydro-7-O-benzoyl-5-O-benzyl-2-deoxy-7-C-phenyl-D-glycero-L-ido-heptono-1,4-lactone

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Chemical Property of 3,6-anhydro-7-O-benzoyl-5-O-benzyl-2-deoxy-7-C-phenyl-D-glycero-L-ido-heptono-1,4-lactone

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Technology Process of 3,6-anhydro-7-O-benzoyl-5-O-benzyl-2-deoxy-7-C-phenyl-D-glycero-L-ido-heptono-1,4-lactone

There total 5 articles about 3,6-anhydro-7-O-benzoyl-5-O-benzyl-2-deoxy-7-C-phenyl-D-glycero-L-ido-heptono-1,4-lactone 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: 64.0%

: 2033-24-1
cycl-isopropylidene malonate

: 5-O-benzoyl-3-O-benzyl-5-C-phenyl-L-ido-pentofuranose

: 1361026-56-3
3,6-anhydro-7-O-benzoyl-5-O-benzyl-2-deoxy-7-C-phenyl-D-glycero-L-ido-heptono-1,4-lactone

Guidance literature:: With triethylamine; In N,N-dimethyl-formamide; at 46 ℃; for 67h;
DOI:10.1016/j.bmcl.2013.08.069

Reference yield:

: 18439-42-4,18439-43-5
3-O-benzyl-1,2-O-isopropylidene-5-C-phenyl-α-L-ido-pentofuranose

: 1361026-56-3
3,6-anhydro-7-O-benzoyl-5-O-benzyl-2-deoxy-7-C-phenyl-D-glycero-L-ido-heptono-1,4-lactone

Guidance literature:: Multi-step reaction with 3 steps

1: pyridine / 18.5 h / 0 - 20 °C

2: trifluoroacetic acid / water / 0.5 h / 20 °C

3: triethylamine / N,N-dimethyl-formamide / 67 h / 46 °C

With pyridine; triethylamine; trifluoroacetic acid; In water; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2013.08.069

Reference yield:

: 65462-15-9
3-O-benzyl-1,2-O-isopropylidene-β-L-arabino-pentodialdo-1,4-furanose

: 1361026-56-3
3,6-anhydro-7-O-benzoyl-5-O-benzyl-2-deoxy-7-C-phenyl-D-glycero-L-ido-heptono-1,4-lactone

Guidance literature:: Multi-step reaction with 4 steps

1: periodic acid / toluene; tetrahydrofuran / 4.5 h / 0 °C / Inert atmosphere

2: pyridine / 18.5 h / 0 - 20 °C

3: trifluoroacetic acid / water / 0.5 h / 20 °C

4: triethylamine / N,N-dimethyl-formamide / 67 h / 46 °C

With pyridine; periodic acid; triethylamine; trifluoroacetic acid; In tetrahydrofuran; water; N,N-dimethyl-formamide; toluene;
DOI:10.1016/j.bmcl.2013.08.069