Phenyl-acetic acid (E)-(1R,2R)-1-((S)-1-benzyloxycarbonylamino-2-methanesulfonyloxy-ethyl)-2-hydroxy-pent-3-enyl ester

Base Information

Chemical Name:Phenyl-acetic acid (E)-(1R,2R)-1-((S)-1-benzyloxycarbonylamino-2-methanesulfonyloxy-ethyl)-2-hydroxy-pent-3-enyl ester
CAS No.:1054650-04-2
Molecular Formula:C₂₄H₂₉NO₈S
Molecular Weight:491.562
Hs Code.:

Synonyms:Phenyl-acetic acid (E)-(1R,2R)-1-((S)-1-benzyloxycarbonylamino-2-methanesulfonyloxy-ethyl)-2-hydroxy-pent-3-enyl ester

Suppliers and Price of Phenyl-acetic acid (E)-(1R,2R)-1-((S)-1-benzyloxycarbonylamino-2-methanesulfonyloxy-ethyl)-2-hydroxy-pent-3-enyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of Phenyl-acetic acid (E)-(1R,2R)-1-((S)-1-benzyloxycarbonylamino-2-methanesulfonyloxy-ethyl)-2-hydroxy-pent-3-enyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Phenyl-acetic acid (E)-(1R,2R)-1-((S)-1-benzyloxycarbonylamino-2-methanesulfonyloxy-ethyl)-2-hydroxy-pent-3-enyl ester

There total 6 articles about Phenyl-acetic acid (E)-(1R,2R)-1-((S)-1-benzyloxycarbonylamino-2-methanesulfonyloxy-ethyl)-2-hydroxy-pent-3-enyl ester 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:

: 117833-92-8
(4S)-3-benzyloxycarbonyl-2,2-dimethyloxazolidine-4-carbaldehyde

: 1054650-04-2
Phenyl-acetic acid (E)-(1R,2R)-1-((S)-1-benzyloxycarbonylamino-2-methanesulfonyloxy-ethyl)-2-hydroxy-pent-3-enyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: MgBr₂*Et₂O / -20 °C

1.2: 95 percent / CH₂Cl₂ / 25 °C

2.1: 93 percent / camphorsulfonic acid; ethylene glycol / tetrahydrofuran / 50 °C

3.1: Et₃N

4.1: DDC; DMAP

5.1: HF

With dmap; camphor-10-sulfonic acid; hydrogen fluoride; ethylene glycol; triethylamine; 2`,3`-dideoxycytidine; magnesium bromide; In tetrahydrofuran; 1.1: complexation / 1.2: Addition / 2.1: Ring cleavage / 3.1: mesylation / 4.1: Esterification / 5.1: desilylation;
DOI:10.1021/ja992274w

Reference yield:

: 213454-11-6
(S)-4-[(E)-(1R,2R)-2-(tert-Butyl-dimethyl-silanyloxy)-1-hydroxy-pent-3-enyl]-2,2-dimethyl-oxazolidine-3-carboxylic acid benzyl ester

: 1054650-04-2
Phenyl-acetic acid (E)-(1R,2R)-1-((S)-1-benzyloxycarbonylamino-2-methanesulfonyloxy-ethyl)-2-hydroxy-pent-3-enyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 93 percent / camphorsulfonic acid; ethylene glycol / tetrahydrofuran / 50 °C

2: Et₃N

3: DDC; DMAP

4: HF

With dmap; camphor-10-sulfonic acid; hydrogen fluoride; ethylene glycol; triethylamine; 2`,3`-dideoxycytidine; In tetrahydrofuran; 1: Ring cleavage / 2: mesylation / 3: Esterification / 4: desilylation;
DOI:10.1021/ja992274w