6-N-benzoyl-9-(2,5-di-O-(tert-butyldimethylsilyl)-3-C-phenylselenocarbonyl-β-D-xylofuranosyl)adenine

Base Information

Chemical Name:6-N-benzoyl-9-(2,5-di-O-(tert-butyldimethylsilyl)-3-C-phenylselenocarbonyl-β-D-xylofuranosyl)adenine
CAS No.:188486-32-0
Molecular Formula:C₃₆H₄₉N₅O₆SeSi₂
Molecular Weight:782.946
Hs Code.:

Synonyms:6-N-benzoyl-9-(2,5-di-O-(tert-butyldimethylsilyl)-3-C-phenylselenocarbonyl-β-D-xylofuranosyl)adenine

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Chemical Property of 6-N-benzoyl-9-(2,5-di-O-(tert-butyldimethylsilyl)-3-C-phenylselenocarbonyl-β-D-xylofuranosyl)adenine

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Technology Process of 6-N-benzoyl-9-(2,5-di-O-(tert-butyldimethylsilyl)-3-C-phenylselenocarbonyl-β-D-xylofuranosyl)adenine

There total 11 articles about 6-N-benzoyl-9-(2,5-di-O-(tert-butyldimethylsilyl)-3-C-phenylselenocarbonyl-β-D-xylofuranosyl)adenine 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:

: 9-(3-C-phenylselenocarbonyl-β-D-xylofuranosyl)adenine

: 188486-32-0
6-N-benzoyl-9-(2,5-di-O-(tert-butyldimethylsilyl)-3-C-phenylselenocarbonyl-β-D-xylofuranosyl)adenine

Guidance literature:: Multi-step reaction with 12 steps

1.1: Bu₃SnH / methanol / 2.5 h / 20 °C / Photolysis

2.1: 50 percent / pyridine / 20 °C

3.1: 100 percent / pyridine / 1 h / 0 - 20 °C

4.1: 100 percent / pyridine / 2 h / 0 - 20 °C

5.1: 100 percent / p-toluenesulfonic acid; EtOH / 1 h / 0 - 20 °C

6.1: 99 percent / Dess-Martin periodinane / CH₂Cl₂ / 72 h / 0 - 20 °C

7.1: CeCl₃ / tetrahydrofuran / 4 h / -78 °C

7.2: 82 percent / tetrahydrofuran / 3 h / -78 °C

8.1: 4.66 g / CH₂Cl₂ / 72 h / 20 °C

9.1: ozone / CH₂Cl₂ / 1 h / -78 °C

9.2: 3.10 g / Me₂S / CH₂Cl₂ / 2 h / -78 - 20 °C

10.1: KMnO₄; phosphate buffer / 2-methyl-propan-2-ol; H₂O / 2 h / 20 °C / pH 7

11.1: 53 mg / HCl; H₂O / 2-methyl-propan-2-ol / 0 °C / pH 3

12.1: 1,1'-carbonyldi-1,2,4-triazole / dimethylformamide / 0 - 20 °C

12.2: 79 percent / dimethylformamide / 1 h / 0 °C

With 1,1'-Carbonyl-di-(1,2,4-triazole); pyridine; hydrogenchloride; potassium permanganate; phosphate buffer; cerium(III) chloride; ethanol; water; tri-n-butyl-tin hydride; Dess-Martin periodane; toluene-4-sulfonic acid; ozone; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; tert-butyl alcohol; 1.1: Reduction / 2.1: silylation / 3.1: silylation / 4.1: benzoylation / 5.1: desilylation / 6.1: Oxidation / 7.1: transmetallation / 7.2: Addition / 8.1: Horning silylation / 9.1: ozonolysis / 9.2: Reduction / 10.1: Oxidation / 11.1: desilylation / 12.1: triazolidation / 12.2: Acylation;
DOI:10.1021/ja962974q

Reference yield:

: 65109-11-7
2',5'-bis-O-(tert-butyldimethylsilyl)adenosine

: 188486-32-0
6-N-benzoyl-9-(2,5-di-O-(tert-butyldimethylsilyl)-3-C-phenylselenocarbonyl-β-D-xylofuranosyl)adenine

Guidance literature:: Multi-step reaction with 10 steps

1.1: 100 percent / pyridine / 1 h / 0 - 20 °C

2.1: 100 percent / pyridine / 2 h / 0 - 20 °C

3.1: 100 percent / p-toluenesulfonic acid; EtOH / 1 h / 0 - 20 °C

4.1: 99 percent / Dess-Martin periodinane / CH₂Cl₂ / 72 h / 0 - 20 °C

5.1: CeCl₃ / tetrahydrofuran / 4 h / -78 °C

5.2: 82 percent / tetrahydrofuran / 3 h / -78 °C

6.1: 4.66 g / CH₂Cl₂ / 72 h / 20 °C

7.1: ozone / CH₂Cl₂ / 1 h / -78 °C

7.2: 3.10 g / Me₂S / CH₂Cl₂ / 2 h / -78 - 20 °C

8.1: KMnO₄; phosphate buffer / 2-methyl-propan-2-ol; H₂O / 2 h / 20 °C / pH 7

9.1: 53 mg / HCl; H₂O / 2-methyl-propan-2-ol / 0 °C / pH 3

10.1: 1,1'-carbonyldi-1,2,4-triazole / dimethylformamide / 0 - 20 °C

10.2: 79 percent / dimethylformamide / 1 h / 0 °C

With 1,1'-Carbonyl-di-(1,2,4-triazole); pyridine; hydrogenchloride; potassium permanganate; phosphate buffer; cerium(III) chloride; ethanol; water; Dess-Martin periodane; toluene-4-sulfonic acid; ozone; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; tert-butyl alcohol; 1.1: silylation / 2.1: benzoylation / 3.1: desilylation / 4.1: Oxidation / 5.1: transmetallation / 5.2: Addition / 6.1: Horning silylation / 7.1: ozonolysis / 7.2: Reduction / 8.1: Oxidation / 9.1: desilylation / 10.1: triazolidation / 10.2: Acylation;
DOI:10.1021/ja962974q

Reference yield:

: 9-[3-(tert-butyl-dimethyl-silanyloxy)-5-(tert-butyl-dimethyl-silanyloxymethyl)-4-trimethylsilanyloxy-tetrahydro-furan-2-yl]-9H-purin-6-ylamine

: 188486-32-0
6-N-benzoyl-9-(2,5-di-O-(tert-butyldimethylsilyl)-3-C-phenylselenocarbonyl-β-D-xylofuranosyl)adenine

Guidance literature:: Multi-step reaction with 9 steps

1.1: 100 percent / pyridine / 2 h / 0 - 20 °C

2.1: 100 percent / p-toluenesulfonic acid; EtOH / 1 h / 0 - 20 °C

3.1: 99 percent / Dess-Martin periodinane / CH₂Cl₂ / 72 h / 0 - 20 °C

4.1: CeCl₃ / tetrahydrofuran / 4 h / -78 °C

4.2: 82 percent / tetrahydrofuran / 3 h / -78 °C

5.1: 4.66 g / CH₂Cl₂ / 72 h / 20 °C

6.1: ozone / CH₂Cl₂ / 1 h / -78 °C

6.2: 3.10 g / Me₂S / CH₂Cl₂ / 2 h / -78 - 20 °C

7.1: KMnO₄; phosphate buffer / 2-methyl-propan-2-ol; H₂O / 2 h / 20 °C / pH 7

8.1: 53 mg / HCl; H₂O / 2-methyl-propan-2-ol / 0 °C / pH 3

9.1: 1,1'-carbonyldi-1,2,4-triazole / dimethylformamide / 0 - 20 °C

9.2: 79 percent / dimethylformamide / 1 h / 0 °C

With 1,1'-Carbonyl-di-(1,2,4-triazole); pyridine; hydrogenchloride; potassium permanganate; phosphate buffer; cerium(III) chloride; ethanol; water; Dess-Martin periodane; toluene-4-sulfonic acid; ozone; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; tert-butyl alcohol; 1.1: benzoylation / 2.1: desilylation / 3.1: Oxidation / 4.1: transmetallation / 4.2: Addition / 5.1: Horning silylation / 6.1: ozonolysis / 6.2: Reduction / 7.1: Oxidation / 8.1: desilylation / 9.1: triazolidation / 9.2: Acylation;
DOI:10.1021/ja962974q