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(R)-17-(tert-Butyl-diphenyl-silanyloxy)-3-((2R,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-heptadecanoic acid

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  • Chemical Name:(R)-17-(tert-Butyl-diphenyl-silanyloxy)-3-((2R,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-heptadecanoic acid
  • CAS No.:404867-98-7
  • Molecular Formula:C60H80O9Si
  • Molecular Weight:973.375
  • Hs Code.:
(R)-17-(tert-Butyl-diphenyl-silanyloxy)-3-((2R,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-heptadecanoic acid

Synonyms:(R)-17-(tert-Butyl-diphenyl-silanyloxy)-3-((2R,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-heptadecanoic acid

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Chemical Property of (R)-17-(tert-Butyl-diphenyl-silanyloxy)-3-((2R,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-heptadecanoic acid
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Technology Process of (R)-17-(tert-Butyl-diphenyl-silanyloxy)-3-((2R,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-heptadecanoic acid

There total 11 articles about (R)-17-(tert-Butyl-diphenyl-silanyloxy)-3-((2R,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-heptadecanoic acid 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:
Guidance literature:
Multi-step reaction with 5 steps
1.1: LDA / hexane; tetrahydrofuran / 1 h / -78 °C
1.2: hexane; tetrahydrofuran / 2 h / -40 °C
1.3: 3.1 g / H2; [RuCl2(COD)]n; Et3N / (R)-BINAP / methanol; tetrahydrofuran / 15 h / 70 °C / 11400 Torr
2.1: 81 percent / imidazole / dimethylformamide / 4 h / 20 °C
3.1: 62 percent / 4A molecular sieves; BF3*Et2O / CH2Cl2 / 2 h / -40 °C
4.1: F3CCO2H / CH2Cl2 / 3 h / 0 - 20 °C
5.1: 585 mg / NH3 / methanol
With 1H-imidazole; 4 A molecular sieve; boron trifluoride diethyl etherate; ammonia; trifluoroacetic acid; lithium diisopropyl amide; In tetrahydrofuran; methanol; hexane; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ja036521e
Guidance literature:
Multi-step reaction with 5 steps
1: 88 percent / H2 / [(R)-BINAP*RuCl2]2*NEt3 / methanol; tetrahydrofuran / 15 h / 70 °C / 11400.8 Torr
2: 81 percent / imidazole / dimethylformamide / 4 h / 20 °C
3: molecular sieves 4 Angstroem; BF3*Et2O / CH2Cl2 / 2 h / -40 °C
4: CF3COOH / CH2Cl2 / 0 - 20 °C
5: 585 mg / NH3 / methanol
With 1H-imidazole; 4 A molecular sieve; boron trifluoride diethyl etherate; ammonia; hydrogen; trifluoroacetic acid; [(R)-BINAP RuCl2]2NEt3; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ja0175791
Guidance literature:
Multi-step reaction with 5 steps
1: 13.5 g / H2NNH2*AcOH / dimethylformamide / 5 h / 20 °C
2: 74 percent / NaH / CH2Cl2 / 2 h
3: 62 percent / 4A molecular sieves; BF3*Et2O / CH2Cl2 / 2 h / -40 °C
4: F3CCO2H / CH2Cl2 / 3 h / 0 - 20 °C
5: 585 mg / NH3 / methanol
With 4 A molecular sieve; boron trifluoride diethyl etherate; ammonia; hydrazinium monoacetate; sodium hydride; trifluoroacetic acid; In methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ja036521e
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