4-pentenyl 3-O-acetyl-2-amino-2-N-benzyloxycarbonyl-2-deoxy-α-D-mannopyranoside

Base Information

Chemical Name:4-pentenyl 3-O-acetyl-2-amino-2-N-benzyloxycarbonyl-2-deoxy-α-D-mannopyranoside
CAS No.:855271-03-3
Molecular Formula:C₂₁H₂₉NO₈
Molecular Weight:423.463
Hs Code.:

Synonyms:4-pentenyl 3-O-acetyl-2-amino-2-N-benzyloxycarbonyl-2-deoxy-α-D-mannopyranoside

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Chemical Property of 4-pentenyl 3-O-acetyl-2-amino-2-N-benzyloxycarbonyl-2-deoxy-α-D-mannopyranoside

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Technology Process of 4-pentenyl 3-O-acetyl-2-amino-2-N-benzyloxycarbonyl-2-deoxy-α-D-mannopyranoside

There total 8 articles about 4-pentenyl 3-O-acetyl-2-amino-2-N-benzyloxycarbonyl-2-deoxy-α-D-mannopyranoside 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: 92.0%

: 855271-01-1
4-pentenyl 3-O-acetyl-2-amino-2-N-benzyloxycarbonyl-2-deoxy-4,6-O-isopropylidene-α-D-mannopyranoside

: 855271-03-3
4-pentenyl 3-O-acetyl-2-amino-2-N-benzyloxycarbonyl-2-deoxy-α-D-mannopyranoside

Guidance literature:: 4-pentenyl 3-O-acetyl-2-amino-2-N-benzyloxycarbonyl-2-deoxy-4,6-O-isopropylidene-α-D-mannopyranoside; With triethylsilyl trifluoromethyl sulfonate; In dichloromethane; water; at 23 ℃;

With triethylamine; In dichloromethane; at 23 ℃;
DOI:10.1021/jo0500129

Reference yield:

: 855270-65-4
3-O-carbamoyl-4,6-O-isopropylidene-D-glucal

: 855271-03-3
4-pentenyl 3-O-acetyl-2-amino-2-N-benzyloxycarbonyl-2-deoxy-α-D-mannopyranoside

Guidance literature:: Multi-step reaction with 5 steps

1.1: iodosobenzene; molecular sieves 4 Angstroem / Rh₂(OAc)4 / CH₂Cl₂ / 25 h / 23 °C

2.1: 92 percent / Et₃N; DMAP / tetrahydrofuran / 4 h / 23 °C

3.1: 70 percent / sodium hydride / methanol; toluene / 0.75 h / -70 - -15 °C

4.1: 93 percent / pyridine; 4-(dimethylamino)pyridine / CH₂Cl₂ / 0 - 23 °C

5.1: Et₃SiOTf / CH₂Cl₂; H₂O / 23 °C

5.2: 92 percent / Et₃N / CH₂Cl₂ / 23 °C

With pyridine; dmap; iodosylbenzene; 4 A molecular sieve; triethylsilyl trifluoromethyl sulfonate; sodium hydride; triethylamine; dirhodium tetraacetate; In tetrahydrofuran; methanol; dichloromethane; water; toluene;
DOI:10.1021/jo0500129

Reference yield:

: 51450-36-3
4,6-O-isopropylidene-D-glucal

: 855271-03-3
4-pentenyl 3-O-acetyl-2-amino-2-N-benzyloxycarbonyl-2-deoxy-α-D-mannopyranoside

Guidance literature:: Multi-step reaction with 6 steps

1.1: CH₂Cl₂ / 0 - 23 °C

1.2: 71 percent / K₂CO₃ / methanol; CH₂Cl₂ / 0 - 23 °C

2.1: iodosobenzene; molecular sieves 4 Angstroem / Rh₂(OAc)4 / CH₂Cl₂ / 25 h / 23 °C

3.1: 92 percent / Et₃N; DMAP / tetrahydrofuran / 4 h / 23 °C

4.1: 70 percent / sodium hydride / methanol; toluene / 0.75 h / -70 - -15 °C

5.1: 93 percent / pyridine; 4-(dimethylamino)pyridine / CH₂Cl₂ / 0 - 23 °C

6.1: Et₃SiOTf / CH₂Cl₂; H₂O / 23 °C

6.2: 92 percent / Et₃N / CH₂Cl₂ / 23 °C

With pyridine; dmap; iodosylbenzene; 4 A molecular sieve; triethylsilyl trifluoromethyl sulfonate; sodium hydride; triethylamine; dirhodium tetraacetate; In tetrahydrofuran; methanol; dichloromethane; water; toluene;
DOI:10.1021/jo0500129