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(2R,3S,4R)-ethyl 4-(tert-butyldiphenylsilyloxy)-2,3-dihydroxyheptanoate

Base Information Edit
  • Chemical Name:(2R,3S,4R)-ethyl 4-(tert-butyldiphenylsilyloxy)-2,3-dihydroxyheptanoate
  • CAS No.:1359984-30-7
  • Molecular Formula:C25H36O5Si
  • Molecular Weight:444.643
  • Hs Code.:
  • Mol file:1359984-30-7.mol
(2R,3S,4R)-ethyl 4-(tert-butyldiphenylsilyloxy)-2,3-dihydroxyheptanoate

Synonyms:(2R,3S,4R)-ethyl 4-(tert-butyldiphenylsilyloxy)-2,3-dihydroxyheptanoate

Suppliers and Price of (2R,3S,4R)-ethyl 4-(tert-butyldiphenylsilyloxy)-2,3-dihydroxyheptanoate
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (2R,3S,4R)-ethyl 4-(tert-butyldiphenylsilyloxy)-2,3-dihydroxyheptanoate Edit
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Technology Process of (2R,3S,4R)-ethyl 4-(tert-butyldiphenylsilyloxy)-2,3-dihydroxyheptanoate

There total 4 articles about (2R,3S,4R)-ethyl 4-(tert-butyldiphenylsilyloxy)-2,3-dihydroxyheptanoate 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:
With methanesulfonamide; AD-mix β; water; In tert-butyl alcohol; at 20 ℃; for 24h;
DOI:10.1016/j.tetlet.2011.12.119
Guidance literature:
Multi-step reaction with 3 steps
1.1: diisobutylaluminium hydride / dichloromethane / -78 °C
2.1: sodium hydride / tetrahydrofuran; mineral oil / 0.25 h / 0 °C
2.2: 0 °C
3.1: AD-mix β; methanesulfonamide; water / tert-butyl alcohol / 24 h / 20 °C
With methanesulfonamide; AD-mix β; water; sodium hydride; diisobutylaluminium hydride; In tetrahydrofuran; dichloromethane; mineral oil; tert-butyl alcohol; 2.1: Horner-Wadsworth-Emmons olefination / 2.2: Horner-Wadsworth-Emmons olefination / 3.1: Sharpless dihydroxylation;
DOI:10.1016/j.tetlet.2011.12.119
Guidance literature:
Multi-step reaction with 4 steps
1.1: 1H-imidazole; dmap / 12 h
2.1: diisobutylaluminium hydride / dichloromethane / -78 °C
3.1: sodium hydride / tetrahydrofuran; mineral oil / 0.25 h / 0 °C
3.2: 0 °C
4.1: AD-mix β; methanesulfonamide; water / tert-butyl alcohol / 24 h / 20 °C
With 1H-imidazole; dmap; methanesulfonamide; AD-mix β; water; sodium hydride; diisobutylaluminium hydride; In tetrahydrofuran; dichloromethane; mineral oil; tert-butyl alcohol; 3.1: Horner-Wadsworth-Emmons olefination / 3.2: Horner-Wadsworth-Emmons olefination / 4.1: Sharpless dihydroxylation;
DOI:10.1016/j.tetlet.2011.12.119
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