2,3-O-isopropylidene-2-C-methyl-D-erythrose-(O-benzyl)oxime 4-dibenzyl phosphate

Base Information

Chemical Name:2,3-O-isopropylidene-2-C-methyl-D-erythrose-(O-benzyl)oxime 4-dibenzyl phosphate
CAS No.:258518-29-5
Molecular Formula:C₂₉H₃₄NO₇P
Molecular Weight:539.565
Hs Code.:

Synonyms:2,3-O-isopropylidene-2-C-methyl-D-erythrose-(O-benzyl)oxime 4-dibenzyl phosphate

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Chemical Property of 2,3-O-isopropylidene-2-C-methyl-D-erythrose-(O-benzyl)oxime 4-dibenzyl phosphate

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Technology Process of 2,3-O-isopropylidene-2-C-methyl-D-erythrose-(O-benzyl)oxime 4-dibenzyl phosphate

There total 5 articles about 2,3-O-isopropylidene-2-C-methyl-D-erythrose-(O-benzyl)oxime 4-dibenzyl phosphate 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: 71.0%

: 176506-97-1
dibenzyl phosphoroiodidate

: 258518-28-4
2,3-O-isopropylidene-2-C-methyl-D-erythrose-(O-benzyl)oxime

: 258518-29-5
2,3-O-isopropylidene-2-C-methyl-D-erythrose-(O-benzyl)oxime 4-dibenzyl phosphate

Guidance literature:: With pyridine; In dichloromethane; at -20 - 20 ℃; for 2h;
DOI:10.1021/jo9905118

Reference yield:

: 15205-57-9
tribenzyl phosphite

: 258518-29-5
2,3-O-isopropylidene-2-C-methyl-D-erythrose-(O-benzyl)oxime 4-dibenzyl phosphate

Guidance literature:: Multi-step reaction with 2 steps

1: I₂ / CH₂Cl₂ / -20 - 20 °C

2: 71 percent / pyridine / CH₂Cl₂ / 2 h / -20 - 20 °C

With pyridine; iodine; In dichloromethane; 1: Iodination / 2: Substitution;
DOI:10.1021/jo9905118

Reference yield:

: 2687-43-6
O-benzylhydoxylamine hydrochloride

: 258518-29-5
2,3-O-isopropylidene-2-C-methyl-D-erythrose-(O-benzyl)oxime 4-dibenzyl phosphate

Guidance literature:: Multi-step reaction with 2 steps

1: 66 percent / pyridine / CH₂Cl₂ / 15 h / 25 °C

2: 71 percent / pyridine / CH₂Cl₂ / 2 h / -20 - 20 °C

With pyridine; In dichloromethane; 1: Ring cleavage / 2: Substitution;
DOI:10.1021/jo9905118