4-O-Benzoyl-2,3-di-O-benzyl-α-L-fucopyranosyl trichloroacetimidate

Base Information

Chemical Name:4-O-Benzoyl-2,3-di-O-benzyl-α-L-fucopyranosyl trichloroacetimidate
CAS No.:1607433-68-0
Molecular Formula:C₂₉H₂₈Cl₃NO₆
Molecular Weight:592.903
Hs Code.:

Synonyms:4-O-Benzoyl-2,3-di-O-benzyl-α-L-fucopyranosyl trichloroacetimidate

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

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Chemical Property of 4-O-Benzoyl-2,3-di-O-benzyl-α-L-fucopyranosyl trichloroacetimidate

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Technology Process of 4-O-Benzoyl-2,3-di-O-benzyl-α-L-fucopyranosyl trichloroacetimidate

There total 1 articles about 4-O-Benzoyl-2,3-di-O-benzyl-α-L-fucopyranosyl trichloroacetimidate 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: 75.0%

: 545-06-2
trichloroacetonitrile

: 2,3-di-O-benzyl-4-O-benzoyl-6-deoxy-α/β-L-galactopyranose

: 1607433-68-0
4-O-Benzoyl-2,3-di-O-benzyl-α-L-fucopyranosyl trichloroacetimidate

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; at 20 ℃; for 5h;
DOI:10.1021/jo500503r

Reference yield: 67.0%

: 1607433-68-0
4-O-Benzoyl-2,3-di-O-benzyl-α-L-fucopyranosyl trichloroacetimidate

: 1607433-71-5
p-Tolyl 4-O-benzoyl-2-O-benzyl-1-thio-β-L-fucopyranoside

: 1607433-78-2
p-Tolyl (4-O-benzoyl-2,3-di-O-benzyl-α-L-fucopyranosyl)-(1→ 3)-4-O-benzoyl-2-O-benzyl-1-thio-β-L-fucopyranoside

: N-(4-O-Benzoyl-2,3-di-O-benzyl-α-L-fucopyranosyl)-trichloroacetamide

Guidance literature:: 4-O-Benzoyl-2,3-di-O-benzyl-α-L-fucopyranosyl trichloroacetimidate; p-Tolyl 4-O-benzoyl-2-O-benzyl-1-thio-β-L-fucopyranoside; In dichloromethane; at 20 ℃; for 1h; Molecular sieve; Inert atmosphere;

With trimethylsilyl trifluoromethanesulfonate; In dichloromethane; at -78 - 0 ℃; for 0.833333h;
DOI:10.1021/jo500503r