5-O-benzyl-3-deoxy-1,2-O-isopropylidene-3-C-p-tolylsulfanyl-α-D-ribofuranose

Base Information

Chemical Name:5-O-benzyl-3-deoxy-1,2-O-isopropylidene-3-C-p-tolylsulfanyl-α-D-ribofuranose
CAS No.:476645-44-0
Molecular Formula:C₂₂H₂₆O₄S
Molecular Weight:386.512
Hs Code.:

Synonyms:5-O-benzyl-3-deoxy-1,2-O-isopropylidene-3-C-p-tolylsulfanyl-α-D-ribofuranose

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Chemical Property of 5-O-benzyl-3-deoxy-1,2-O-isopropylidene-3-C-p-tolylsulfanyl-α-D-ribofuranose

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Technology Process of 5-O-benzyl-3-deoxy-1,2-O-isopropylidene-3-C-p-tolylsulfanyl-α-D-ribofuranose

There total 1 articles about 5-O-benzyl-3-deoxy-1,2-O-isopropylidene-3-C-p-tolylsulfanyl-α-D-ribofuranose 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: 59.0%

: 106-45-6
para-thiocresol

: 5-O-benzyl-1,2-O-isopropylidene-3-O-tosyl-α-D-xylofuranose

: 476645-44-0
5-O-benzyl-3-deoxy-1,2-O-isopropylidene-3-C-p-tolylsulfanyl-α-D-ribofuranose

Guidance literature:: With sodium methylate; In N,N-dimethyl-formamide; at 115 - 120 ℃; for 4h;
DOI:10.1055/s-2002-32960

Reference yield: 55.0%

: 67-56-1
methanol

: 476645-44-0
5-O-benzyl-3-deoxy-1,2-O-isopropylidene-3-C-p-tolylsulfanyl-α-D-ribofuranose

: 476645-46-2
methyl 5-O-benzyl-3-deoxy-3-C-p-tolylsulfanyl-β-D-ribofuranoside

: 476645-45-1
methyl 5-O-benzyl-3-deoxy-3-C-p-tolylsulfanyl-α-D-ribofuranoside

Guidance literature:: With sulfuric acid; for 3.5h; Heating;
DOI:10.1016/S0040-4020(03)01059-7

Reference yield:

: 476645-44-0
5-O-benzyl-3-deoxy-1,2-O-isopropylidene-3-C-p-tolylsulfanyl-α-D-ribofuranose

: 476645-50-8
methyl 5-O-benzyl-2,3-dideoxy-3-C-(p)-tolylsulfonyl-β-D-erythro-pent-2-enofuranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 55 percent / H₂SO₄ / 3.5 h / Heating

2: 93 percent / magnesium monoperoxyphthalate / methanol / 3 h / 20 °C

3: 92 percent / MsCl; pyridine / 24 h / 4 °C

With pyridine; sulfuric acid; magnesium monoperoxyphthalate hexahydrate; methanesulfonyl chloride; In methanol;
DOI:10.1016/S0040-4020(03)01059-7