tert-butyl 6-O-benzyl-2,3,4-trideoxy-4-N-(nosylamino)-β-D-threo-hex-2-enopyranoside

Base Information

Chemical Name:tert-butyl 6-O-benzyl-2,3,4-trideoxy-4-N-(nosylamino)-β-D-threo-hex-2-enopyranoside
CAS No.:933066-57-0
Molecular Formula:C₂₃H₂₈N₂O₇S
Molecular Weight:476.551
Hs Code.:

Synonyms:tert-butyl 6-O-benzyl-2,3,4-trideoxy-4-N-(nosylamino)-β-D-threo-hex-2-enopyranoside

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Chemical Property of tert-butyl 6-O-benzyl-2,3,4-trideoxy-4-N-(nosylamino)-β-D-threo-hex-2-enopyranoside

Chemical Property:

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Technology Process of tert-butyl 6-O-benzyl-2,3,4-trideoxy-4-N-(nosylamino)-β-D-threo-hex-2-enopyranoside

There total 2 articles about tert-butyl 6-O-benzyl-2,3,4-trideoxy-4-N-(nosylamino)-β-D-threo-hex-2-enopyranoside 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:

: 933066-42-3
6-O-benzyl-3-deoxy-3-N-(nosylamino)-D-glucal

: 933066-57-0
tert-butyl 6-O-benzyl-2,3,4-trideoxy-4-N-(nosylamino)-β-D-threo-hex-2-enopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 51 percent / pyridine / CH₂Cl₂ / 18 h / 0 °C

2: 70 percent / K₂CO₃ / acetonitrile / 3 h / 20 °C

With pyridine; potassium carbonate; In dichloromethane; acetonitrile;
DOI:10.1016/j.tet.2006.12.069

Reference yield:

: 1694-92-4
2-Nitrobenzenesulfonyl chloride

: 933066-57-0
tert-butyl 6-O-benzyl-2,3,4-trideoxy-4-N-(nosylamino)-β-D-threo-hex-2-enopyranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 80 percent / Et₃N / CH₂Cl₂ / 3 h / 20 °C

2: 51 percent / pyridine / CH₂Cl₂ / 18 h / 0 °C

3: 70 percent / K₂CO₃ / acetonitrile / 3 h / 20 °C

With pyridine; potassium carbonate; triethylamine; In dichloromethane; acetonitrile;
DOI:10.1016/j.tet.2006.12.069