C₂₉H₅₀O₅Si

Base Information

Chemical Name:C₂₉H₅₀O₅Si
CAS No.:955030-30-5
Molecular Formula:C₂₉H₅₀O₅Si
Molecular Weight:506.798
Hs Code.:

C<sub>29</sub>H<sub>50</sub>O<sub>5</sub>Si

Synonyms:C₂₉H₅₀O₅Si

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Chemical Property of C₂₉H₅₀O₅Si

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Technology Process of C₂₉H₅₀O₅Si

There total 8 articles about C₂₉H₅₀O₅Si 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: 90.0%

: 955030-44-1
C₃₉H₅₇NO₇Si

: 955030-30-5
C₂₉H₅₀O₅Si

Guidance literature:: With sodium tetrahydroborate; In tetrahydrofuran; water;
DOI:10.1016/j.tetlet.2007.07.156

Reference yield:

: 955030-28-1
C₃₆H₅₁NO₆Si

: 955030-30-5
C₂₉H₅₀O₅Si

Guidance literature:: Multi-step reaction with 4 steps

1: 75 percent / NaBH₄ / tetrahydrofuran; H₂O

2: 85 percent / TEMPO; IBDA / CH₂Cl₂

3: 90 percent / TiCl₄; (-)-Sparteine / CH₂Cl₂ / 0 °C

4: 90 percent / NaBH₄ / tetrahydrofuran; H₂O

With 2,2,6,6-tetramethyl-piperidine-N-oxyl; sodium tetrahydroborate; titanium tetrachloride; (-)-sparteine; In tetrahydrofuran; dichloromethane; water; 3: Crimmins asymmetric aldol reaction;
DOI:10.1016/j.tetlet.2007.07.156

Reference yield:

: 955030-42-9
C₃₀H₃₇NO₆

: 955030-30-5
C₂₉H₅₀O₅Si

Guidance literature:: Multi-step reaction with 5 steps

1: 90 percent / imidazole / dimethylformamide

2: 75 percent / NaBH₄ / tetrahydrofuran; H₂O

3: 85 percent / TEMPO; IBDA / CH₂Cl₂

4: 90 percent / TiCl₄; (-)-Sparteine / CH₂Cl₂ / 0 °C

5: 90 percent / NaBH₄ / tetrahydrofuran; H₂O

With 1H-imidazole; 2,2,6,6-tetramethyl-piperidine-N-oxyl; sodium tetrahydroborate; titanium tetrachloride; (-)-sparteine; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; 4: Crimmins asymmetric aldol reaction;
DOI:10.1016/j.tetlet.2007.07.156