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C46H56N4O8SSi

Base Information Edit
  • Chemical Name:C46H56N4O8SSi
  • CAS No.:911677-82-2
  • Molecular Formula:C46H56N4O8SSi
  • Molecular Weight:853.124
  • Hs Code.:
  • Mol file:911677-82-2.mol
C<sub>46</sub>H<sub>56</sub>N<sub>4</sub>O<sub>8</sub>SSi

Synonyms:C46H56N4O8SSi

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Chemical Property of C46H56N4O8SSi Edit
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Technology Process of C46H56N4O8SSi

There total 10 articles about C46H56N4O8SSi 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:
4-{3-methoxy-5-oxo-2-[1-(toluene-4-sulfonyl)-1H-indol-3-yl]-9-triisopropylsilanyloxy-8,9-dihydro-5H-cycloheptapyrazin-6-yl}-2,2-dimethyl-5-vinyl-oxazole-3-carboxylic acid tert-butyl ester; In (2)H8-toluene; at 110 ℃; for 2h;
With 2,3-dicyano-5,6-dichloro-p-benzoquinone; at 20 ℃; for 2h;
DOI:10.1021/ol0617547
Guidance literature:
Multi-step reaction with 9 steps
1.1: 86 percent / imidazole / dimethylformamide / 16 h / 40 °C
2.1: 85 percent / LiCl; CuCl / Pd(PPh3)4 / dimethylsulfoxide / 0.5 h / 20 °C
3.1: 82 percent / NaOAc / Pd(PPh3)4 / dimethylformamide / 2 h / 150 °C
4.1: 80 percent / N-methylmorpholine-N-oxide; OsO4; NaIO4 / tetrahydrofuran; H2O / 20 h / 20 °C
5.1: Pd(OAc)2 / acetonitrile / 20 h / 20 °C
6.1: 917 mg / LiHMDS / tetrahydrofuran / -78 - -50 °C
7.1: 86 percent / iodine / CCl4; pyridine / 24 h / 20 °C
8.1: 71 percent / LiCl; CuCl / Pd(PPh3)4 / dimethylsulfoxide / 0.5 h / 20 °C
9.1: toluene-d8 / 2 h / 110 °C
9.2: 72 percent / DDQ / 2 h / 20 °C
With 1H-imidazole; sodium periodate; osmium(VIII) oxide; iodine; sodium acetate; 4-methylmorpholine N-oxide; copper(l) chloride; lithium chloride; lithium hexamethyldisilazane; palladium diacetate; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; pyridine; tetrachloromethane; (2)H8-toluene; water; dimethyl sulfoxide; N,N-dimethyl-formamide; acetonitrile; 2.1: Stille coupling reaction / 3.1: Heck reaction / 4.1: Saegusa oxidation / 5.1: Saegusa oxidation / 8.1: Stille coupling reaction;
DOI:10.1021/ol0617547
Guidance literature:
Multi-step reaction with 8 steps
1.1: 85 percent / LiCl; CuCl / Pd(PPh3)4 / dimethylsulfoxide / 0.5 h / 20 °C
2.1: 82 percent / NaOAc / Pd(PPh3)4 / dimethylformamide / 2 h / 150 °C
3.1: 80 percent / N-methylmorpholine-N-oxide; OsO4; NaIO4 / tetrahydrofuran; H2O / 20 h / 20 °C
4.1: Pd(OAc)2 / acetonitrile / 20 h / 20 °C
5.1: 917 mg / LiHMDS / tetrahydrofuran / -78 - -50 °C
6.1: 86 percent / iodine / CCl4; pyridine / 24 h / 20 °C
7.1: 71 percent / LiCl; CuCl / Pd(PPh3)4 / dimethylsulfoxide / 0.5 h / 20 °C
8.1: toluene-d8 / 2 h / 110 °C
8.2: 72 percent / DDQ / 2 h / 20 °C
With sodium periodate; osmium(VIII) oxide; iodine; sodium acetate; 4-methylmorpholine N-oxide; copper(l) chloride; lithium chloride; lithium hexamethyldisilazane; palladium diacetate; tetrakis(triphenylphosphine) palladium(0); In tetrahydrofuran; pyridine; tetrachloromethane; (2)H8-toluene; water; dimethyl sulfoxide; N,N-dimethyl-formamide; acetonitrile; 1.1: Stille coupling reaction / 2.1: Heck reaction / 3.1: Saegusa oxidation / 4.1: Saegusa oxidation / 7.1: Stille coupling reaction;
DOI:10.1021/ol0617547
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