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C32H42O4Si

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C<sub>32</sub>H<sub>42</sub>O<sub>4</sub>Si

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Chemical Property of C32H42O4Si Edit
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Technology Process of C32H42O4Si

There total 8 articles about C32H42O4Si 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:
1-O-[(tert-butyl)diphenylsilyl]-2,4-dideoxy-2-ethyl-3-O-(4-methoxybenzyl)-4-methyl-L-arabinitol; With oxalyl dichloride; dimethyl sulfoxide; In dichloromethane; at -78 ℃; for 1h;
With triethylamine; In dichloromethane; at -30 ℃;
DOI:10.1002/hlca.201300326
Guidance literature:
Multi-step reaction with 7 steps
1.1: 1H-imidazole / dichloromethane / 3 h / 0 - 20 °C
2.1: diisobutylaluminium hydride / dichloromethane; hexane / 2 h / -10 - 0 °C
3.1: D-(-)-diisopropyl tartrate; titanium(IV) isopropylate; Cumene hydroperoxide / dichloromethane / 3 h / -20 °C / Molecular sieve
4.1: copper(l) iodide / hexane; diethyl ether / 20 h / -20 °C
4.2: 10 h / 20 °C
5.1: toluene-4-sulfonic acid / dichloromethane / 2 h / 20 °C
6.1: diisobutylaluminium hydride / dichloromethane; hexane / 3 h / -20 - 0 °C
7.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / 1 h / -78 °C
7.2: -30 °C
With 1H-imidazole; titanium(IV) isopropylate; copper(l) iodide; oxalyl dichloride; Cumene hydroperoxide; diisobutylaluminium hydride; D-(-)-diisopropyl tartrate; toluene-4-sulfonic acid; dimethyl sulfoxide; In diethyl ether; hexane; dichloromethane; 3.1: |Sharpless Asymmetric Epoxidation / 7.1: |Swern Oxidation / 7.2: |Swern Oxidation;
DOI:10.1002/hlca.201300326
Guidance literature:
Multi-step reaction with 9 steps
1.1: sodium periodate; sodium hydrogencarbonate / dichloromethane; water / 10 h / 0 - 20 °C
2.1: dichloromethane / 3 h / 0 - 20 °C
3.1: 1H-imidazole / dichloromethane / 3 h / 0 - 20 °C
4.1: diisobutylaluminium hydride / dichloromethane; hexane / 2 h / -10 - 0 °C
5.1: D-(-)-diisopropyl tartrate; titanium(IV) isopropylate; Cumene hydroperoxide / dichloromethane / 3 h / -20 °C / Molecular sieve
6.1: copper(l) iodide / hexane; diethyl ether / 20 h / -20 °C
6.2: 10 h / 20 °C
7.1: toluene-4-sulfonic acid / dichloromethane / 2 h / 20 °C
8.1: diisobutylaluminium hydride / dichloromethane; hexane / 3 h / -20 - 0 °C
9.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / 1 h / -78 °C
9.2: -30 °C
With 1H-imidazole; titanium(IV) isopropylate; sodium periodate; copper(l) iodide; oxalyl dichloride; Cumene hydroperoxide; diisobutylaluminium hydride; sodium hydrogencarbonate; D-(-)-diisopropyl tartrate; toluene-4-sulfonic acid; dimethyl sulfoxide; In diethyl ether; hexane; dichloromethane; water; 2.1: |Wittig Olefination / 5.1: |Sharpless Asymmetric Epoxidation / 9.1: |Swern Oxidation / 9.2: |Swern Oxidation;
DOI:10.1002/hlca.201300326
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