allyl 3-O-<(R)-3-benzyloxytetradecanoyl>-2-<(R)-3-benzyloxytetradecanoylamino>-2-deoxy-α-D-glucopyranoside

Base Information

Chemical Name:allyl 3-O-<(R)-3-benzyloxytetradecanoyl>-2-<(R)-3-benzyloxytetradecanoylamino>-2-deoxy-α-D-glucopyranoside
CAS No.:98889-63-5
Molecular Formula:C₅₁H₈₁NO₉
Molecular Weight:852.205
Hs Code.:

Synonyms:allyl 3-O-<(R)-3-benzyloxytetradecanoyl>-2-<(R)-3-benzyloxytetradecanoylamino>-2-deoxy-α-D-glucopyranoside

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Chemical Property of allyl 3-O-<(R)-3-benzyloxytetradecanoyl>-2-<(R)-3-benzyloxytetradecanoylamino>-2-deoxy-α-D-glucopyranoside

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Technology Process of allyl 3-O-<(R)-3-benzyloxytetradecanoyl>-2-<(R)-3-benzyloxytetradecanoylamino>-2-deoxy-α-D-glucopyranoside

There total 7 articles about allyl 3-O-<(R)-3-benzyloxytetradecanoyl>-2-<(R)-3-benzyloxytetradecanoylamino>-2-deoxy-α-D-glucopyranoside 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:

: 98870-61-2
(R)-3-Benzyloxy-tetradecanoic acid (4aR,6S,7R,8R,8aS)-6-allyloxy-7-((R)-3-benzyloxy-tetradecanoylamino)-2,2-dimethyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yl ester

: 98889-63-5
allyl 3-O-<(R)-3-benzyloxytetradecanoyl>-2-<(R)-3-benzyloxytetradecanoylamino>-2-deoxy-α-D-glucopyranoside

Guidance literature:: With acetic acid; at 100 ℃; for 0.5h; Yield given;
DOI:10.1246/bcsj.60.2205

Reference yield:

: 97562-24-8
allyl 2-deoxy-4,6-O-isopropylidene-2-(2,2,2-trichloroethoxycarbonylamino)-α-D-glucopyranoside

: 98889-63-5
allyl 3-O-<(R)-3-benzyloxytetradecanoyl>-2-<(R)-3-benzyloxytetradecanoylamino>-2-deoxy-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1: 64 percent / DCC, DMAP / CH₂Cl₂ / 1 h / Ambient temperature

2: 1.) zinc powder, acetic acid, 2.) triethylamine / 1.) room temp., 30 min, 2.) chloroform

3: DCC / CHCl₃ / 0.5 h / Ambient temperature

4: 90percent acetic acid / 0.5 h / 100 °C

With dmap; acetic acid; triethylamine; dicyclohexyl-carbodiimide; zinc; In dichloromethane; chloroform;
DOI:10.1246/bcsj.60.2205

Reference yield:

: 87357-67-3
(R)-3-benzyloxytetradecanoic acid

: 98889-63-5
allyl 3-O-<(R)-3-benzyloxytetradecanoyl>-2-<(R)-3-benzyloxytetradecanoylamino>-2-deoxy-α-D-glucopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1: 64 percent / DCC, DMAP / CH₂Cl₂ / 1 h / Ambient temperature

2: 1.) zinc powder, acetic acid, 2.) triethylamine / 1.) room temp., 30 min, 2.) chloroform

3: DCC / CHCl₃ / 0.5 h / Ambient temperature

4: 90percent acetic acid / 0.5 h / 100 °C

With dmap; acetic acid; triethylamine; dicyclohexyl-carbodiimide; zinc; In dichloromethane; chloroform;
DOI:10.1246/bcsj.60.2205