(4S,5S)-3-(tert-butoxycarbonyl)-2,2-dimethyl-4-phenyl-1,3-oxazolidine-5-acetic acid

Base Information

Chemical Name:(4S,5S)-3-(tert-butoxycarbonyl)-2,2-dimethyl-4-phenyl-1,3-oxazolidine-5-acetic acid
CAS No.:160237-89-8
Molecular Formula:C₁₈H₂₅NO₅
Molecular Weight:335.4
Hs Code.:

Synonyms:(4S,5S)-3-(tert-butoxycarbonyl)-2,2-dimethyl-4-phenyl-1,3-oxazolidine-5-acetic acid

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Chemical Property of (4S,5S)-3-(tert-butoxycarbonyl)-2,2-dimethyl-4-phenyl-1,3-oxazolidine-5-acetic acid

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Technology Process of (4S,5S)-3-(tert-butoxycarbonyl)-2,2-dimethyl-4-phenyl-1,3-oxazolidine-5-acetic acid

There total 1 articles about (4S,5S)-3-(tert-butoxycarbonyl)-2,2-dimethyl-4-phenyl-1,3-oxazolidine-5-acetic acid 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: 43.0%

: 160237-88-7
(4S,5S)-3-(tert-butoxycarbonyl)-2,2-dimethyl-4-phenyl-5-(2'-propenyl)-1,3-oxazolidine

: 160237-89-8
(4S,5S)-3-(tert-butoxycarbonyl)-2,2-dimethyl-4-phenyl-1,3-oxazolidine-5-acetic acid

Guidance literature:: With ruthenium trichloride; sodium periodate; sodium hydrogencarbonate; In tetrachloromethane; water; acetonitrile; for 48h; Ambient temperature;

Reference yield: 56.0%

: 95603-44-4
7,10-di-(2,2,2-trichloroethyloxycarbonyl)-10-deacetylbaccatin III

: 160237-89-8
(4S,5S)-3-(tert-butoxycarbonyl)-2,2-dimethyl-4-phenyl-1,3-oxazolidine-5-acetic acid

: 160237-90-1
C₅₃H₆₁Cl₆NO₁₈

Guidance literature:: With dmap; dicyclohexyl-carbodiimide; In toluene; at 80 ℃; for 2h;

Reference yield:

: 160237-89-8
(4S,5S)-3-(tert-butoxycarbonyl)-2,2-dimethyl-4-phenyl-1,3-oxazolidine-5-acetic acid

: 160237-91-2
10-deacetyl-3'-N-debenzoyl-7,10-bis<<(2,2,2-trichloroethyl)oxy>carbonyl>-1a'-homotaxol

Guidance literature:: Multi-step reaction with 2 steps

1: 56 percent / DCC, DMAP / toluene / 2 h / 80 °C

2: 73 percent / 90percent formic acid / 4 h / Ambient temperature

With dmap; formic acid; dicyclohexyl-carbodiimide; In toluene;