benzyl 2,4,6-tri-O-benzyl-3-deoxy-3-C-[(7,8,9-tri-O-acetyl-2,6-anhydro-4,5-O-carbonylidene-1,3-dideoxy-1-phenylselenyl-D-erythro-L-talo-nonit-2-yl)-methyl]-β-D-galacto-hexopyranoside

Base Information

Chemical Name:benzyl 2,4,6-tri-O-benzyl-3-deoxy-3-C-[(7,8,9-tri-O-acetyl-2,6-anhydro-4,5-O-carbonylidene-1,3-dideoxy-1-phenylselenyl-D-erythro-L-talo-nonit-2-yl)-methyl]-β-D-galacto-hexopyranoside
CAS No.:352211-97-3
Molecular Formula:C₅₇H₆₂O₁₅Se
Molecular Weight:1066.07
Hs Code.:

benzyl 2,4,6-tri-O-benzyl-3-deoxy-3-C-[(7,8,9-tri-O-acetyl-2,6-anhydro-4,5-O-carbonylidene-1,3-dideoxy-1-phenylselenyl-D-erythro-L-talo-nonit-2-yl)-methyl]-β-D-galacto-hexopyranoside

Synonyms:benzyl 2,4,6-tri-O-benzyl-3-deoxy-3-C-[(7,8,9-tri-O-acetyl-2,6-anhydro-4,5-O-carbonylidene-1,3-dideoxy-1-phenylselenyl-D-erythro-L-talo-nonit-2-yl)-methyl]-β-D-galacto-hexopyranoside

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Chemical Property of benzyl 2,4,6-tri-O-benzyl-3-deoxy-3-C-[(7,8,9-tri-O-acetyl-2,6-anhydro-4,5-O-carbonylidene-1,3-dideoxy-1-phenylselenyl-D-erythro-L-talo-nonit-2-yl)-methyl]-β-D-galacto-hexopyranoside

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Technology Process of benzyl 2,4,6-tri-O-benzyl-3-deoxy-3-C-[(7,8,9-tri-O-acetyl-2,6-anhydro-4,5-O-carbonylidene-1,3-dideoxy-1-phenylselenyl-D-erythro-L-talo-nonit-2-yl)-methyl]-β-D-galacto-hexopyranoside

There total 10 articles about benzyl 2,4,6-tri-O-benzyl-3-deoxy-3-C-[(7,8,9-tri-O-acetyl-2,6-anhydro-4,5-O-carbonylidene-1,3-dideoxy-1-phenylselenyl-D-erythro-L-talo-nonit-2-yl)-methyl]-β-D-galacto-hexopyranoside 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:

: 108-24-7
acetic anhydride

: (3aS,4S,7aS)-6-Phenylselanylmethyl-4-((1R,2R)-1,2,3-trihydroxy-propyl)-6-((2R,3R,4S,5R,6R)-2,3,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-4-ylmethyl)-tetrahydro-[1,3]dioxolo[4,5-c]pyran-2-one

: benzyl 2,4,6-tri-O-benzyl-3-deoxy-3-C-[(7,8,9-tri-O-acetyl-2,6-anhydro-4,5-O-carbonylidene-1,3-dideoxy-1-phenylselenyl-D-erythro-L-galacto-nonit-2-yl)-methyl]-β-D-galacto-hexopyranoside

: 352211-97-3
benzyl 2,4,6-tri-O-benzyl-3-deoxy-3-C-[(7,8,9-tri-O-acetyl-2,6-anhydro-4,5-O-carbonylidene-1,3-dideoxy-1-phenylselenyl-D-erythro-L-talo-nonit-2-yl)-methyl]-β-D-galacto-hexopyranoside

Guidance literature:: With pyridine; In dichloromethane; at 20 ℃;
DOI:10.1021/jo015543l

Reference yield:

: (4S,5R)-4,5-Bis-(tert-butyl-dimethyl-silanyloxy)-5-((4R,5S,4'R)-2,2,2',2'-tetramethyl-[4,4']bi[[1,3]dioxolanyl]-5-yl)-1-((2R,3R,4S,5R,6R)-2,3,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-4-yl)-pentan-2-ol

: 352211-97-3
benzyl 2,4,6-tri-O-benzyl-3-deoxy-3-C-[(7,8,9-tri-O-acetyl-2,6-anhydro-4,5-O-carbonylidene-1,3-dideoxy-1-phenylselenyl-D-erythro-L-talo-nonit-2-yl)-methyl]-β-D-galacto-hexopyranoside

Guidance literature:: Multi-step reaction with 7 steps

1: 95 percent / Dess-Martin-periodinane / CH₂Cl₂

2: 62 percent / toluene; tetrahydrofuran / -40 - 20 °C

3: 94 percent / TBAF / tetrahydrofuran / 40 °C

4: 95 percent / pyridine / CH₂Cl₂ / 0 - 20 °C

5: 69 percent / aq. TFA / tetrahydrofuran / 0.83 h / Heating

6: various solvent(s) / 1 h / -80 °C

7: 317 mg / pyridine / CH₂Cl₂ / 20 °C

With pyridine; tetrabutyl ammonium fluoride; Dess-Martin periodane; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; toluene;
DOI:10.1021/jo015543l

Reference yield:

: 352211-86-0
benzyl 2,4,6-tri-O-benzyl-3-deoxy-3-C-[1,2,3-trideoxy-6,7:8,9-di-O-isopropylidene-2-methylene-D-glycero-D-gulo-non-2-ulos-1-yl]-β-D-galacto-hexopyranoside

: 352211-97-3
benzyl 2,4,6-tri-O-benzyl-3-deoxy-3-C-[(7,8,9-tri-O-acetyl-2,6-anhydro-4,5-O-carbonylidene-1,3-dideoxy-1-phenylselenyl-D-erythro-L-talo-nonit-2-yl)-methyl]-β-D-galacto-hexopyranoside

Guidance literature:: Multi-step reaction with 4 steps

1: 95 percent / pyridine / CH₂Cl₂ / 0 - 20 °C

2: 69 percent / aq. TFA / tetrahydrofuran / 0.83 h / Heating

3: various solvent(s) / 1 h / -80 °C

4: 317 mg / pyridine / CH₂Cl₂ / 20 °C

With pyridine; trifluoroacetic acid; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jo015543l