4,5-di-O-benzyl-6-methyl-L-galacto-(2R)-hydroxy-1,2λ⁵-oxaphosphorinan-2-one

Base Information

Chemical Name:4,5-di-O-benzyl-6-methyl-L-galacto-(2R)-hydroxy-1,2λ⁵-oxaphosphorinan-2-one
CAS No.:266677-33-2
Molecular Formula:C₁₉H₂₃O₆P
Molecular Weight:378.362
Hs Code.:

4,5-di-O-benzyl-6-methyl-L-galacto-(2R)-hydroxy-1,2λ<sup>5</sup>-oxaphosphorinan-2-one

Synonyms:4,5-di-O-benzyl-6-methyl-L-galacto-(2R)-hydroxy-1,2λ⁵-oxaphosphorinan-2-one

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Chemical Property of 4,5-di-O-benzyl-6-methyl-L-galacto-(2R)-hydroxy-1,2λ⁵-oxaphosphorinan-2-one

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Technology Process of 4,5-di-O-benzyl-6-methyl-L-galacto-(2R)-hydroxy-1,2λ⁵-oxaphosphorinan-2-one

There total 3 articles about 4,5-di-O-benzyl-6-methyl-L-galacto-(2R)-hydroxy-1,2λ⁵-oxaphosphorinan-2-one 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: 80.0%

: 266677-30-9
4,5-di-O-benzyl-6-methyl-L-galacto-(2S)-methoxy-1,2λ⁵-oxaphosphorinan-2-one

: 266677-33-2
4,5-di-O-benzyl-6-methyl-L-galacto-(2R)-hydroxy-1,2λ⁵-oxaphosphorinan-2-one

Guidance literature:: With trimethylsilyl bromide; In dichloromethane; at 20 ℃;
DOI:10.1021/jo991696l

Reference yield: 80.0%

: 266677-29-6
4,5-di-O-benzyl-6-methyl-L-galacto-(2R)-methoxy-1,2λ⁵-oxaphosphorinan-2-one

: 266677-33-2
4,5-di-O-benzyl-6-methyl-L-galacto-(2R)-hydroxy-1,2λ⁵-oxaphosphorinan-2-one

Guidance literature:: With trimethylsilyl bromide; In dichloromethane; at 20 ℃;
DOI:10.1021/jo991696l

Reference yield:

: 266677-27-4
2,3-di-O-benzyl-5-deoxy-1-dimethylphosphonyl-4-O-formyl-L-fucose

: 266677-33-2
4,5-di-O-benzyl-6-methyl-L-galacto-(2R)-hydroxy-1,2λ⁵-oxaphosphorinan-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 35 mg / CH₃ONa / methanol / 2 h

2: 80 percent / Me₃SiBr / CH₂Cl₂ / 20 °C

With trimethylsilyl bromide; sodium methylate; In methanol; dichloromethane; 1: Cyclization / 2: phosphonic ester cleavage;
DOI:10.1021/jo991696l