(1R,2S,3S,4R)-1-amino-2,3,4-tri-O-benzyl-5-(benzyloxymethyl)-cyclohex-5-ene-2,3,4-triol

Base Information

Chemical Name:(1R,2S,3S,4R)-1-amino-2,3,4-tri-O-benzyl-5-(benzyloxymethyl)-cyclohex-5-ene-2,3,4-triol
CAS No.:128573-02-4
Molecular Formula:C₃₅H₃₇NO₄
Molecular Weight:535.683
Hs Code.:

Synonyms:(1R,2S,3S,4R)-1-amino-2,3,4-tri-O-benzyl-5-(benzyloxymethyl)-cyclohex-5-ene-2,3,4-triol

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Chemical Property of (1R,2S,3S,4R)-1-amino-2,3,4-tri-O-benzyl-5-(benzyloxymethyl)-cyclohex-5-ene-2,3,4-triol

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Technology Process of (1R,2S,3S,4R)-1-amino-2,3,4-tri-O-benzyl-5-(benzyloxymethyl)-cyclohex-5-ene-2,3,4-triol

There total 5 articles about (1R,2S,3S,4R)-1-amino-2,3,4-tri-O-benzyl-5-(benzyloxymethyl)-cyclohex-5-ene-2,3,4-triol 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: 92.0%

: 128573-01-3
1D-(1,3/2,6)-6-azido-4-benzyloxymethyl-1,2,3-tri-O-benzyltrihydroxycyclohex-4-ene

: 128573-02-4
(1R,2S,3S,4R)-1-amino-2,3,4-tri-O-benzyl-5-(benzyloxymethyl)-cyclohex-5-ene-2,3,4-triol

Guidance literature:: With pyridine; hydrogen sulfide; triethylamine; In water; for 2h;
DOI:10.1071/C96151

Reference yield: 89.0%

: 1045730-69-5
(1R,2S,3S,4R)-2,3,4-tri-O-benzyl-5-(benzyloxymethyl)-1-phthalimidocyclohex-5-ene-2,3,4-triol

: 128573-02-4
(1R,2S,3S,4R)-1-amino-2,3,4-tri-O-benzyl-5-(benzyloxymethyl)-cyclohex-5-ene-2,3,4-triol

Guidance literature:: With ethylenediamine; In ethanol; at 70 ℃; for 3h;
DOI:10.1016/j.carres.2008.04.010

Reference yield:

: 3587-60-8
Benzyloxymethyl chloride

: 128573-02-4
(1R,2S,3S,4R)-1-amino-2,3,4-tri-O-benzyl-5-(benzyloxymethyl)-cyclohex-5-ene-2,3,4-triol

Guidance literature:: Multi-step reaction with 3 steps

2: 48 percent / Pd(PPh₃)4, NaN₃ / tetrahydrofuran / 2 h / Heating

3: 78 percent / PPh₃ / 1 h / Ambient temperature

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium azide; triphenylphosphine; In tetrahydrofuran;