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(20R)-1α-[(tert-butyldimethylsilyl)oxy]-2-oxo-22-thia-25-[(methoxymethyl)oxy]-26,27-dimethyl-16-ene-19,24-dinorvitamin D3 tert-butyldimethylsilyl ether

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  • Chemical Name:(20R)-1α-[(tert-butyldimethylsilyl)oxy]-2-oxo-22-thia-25-[(methoxymethyl)oxy]-26,27-dimethyl-16-ene-19,24-dinorvitamin D3 tert-butyldimethylsilyl ether
  • CAS No.:908862-31-7
  • Molecular Formula:C40H72O5SSi2
  • Molecular Weight:721.246
  • Hs Code.:
  • Mol file:908862-31-7.mol
(20R)-1α-[(tert-butyldimethylsilyl)oxy]-2-oxo-22-thia-25-[(methoxymethyl)oxy]-26,27-dimethyl-16-ene-19,24-dinorvitamin D<sub>3</sub> tert-butyldimethylsilyl ether

Synonyms:(20R)-1α-[(tert-butyldimethylsilyl)oxy]-2-oxo-22-thia-25-[(methoxymethyl)oxy]-26,27-dimethyl-16-ene-19,24-dinorvitamin D3 tert-butyldimethylsilyl ether

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Chemical Property of (20R)-1α-[(tert-butyldimethylsilyl)oxy]-2-oxo-22-thia-25-[(methoxymethyl)oxy]-26,27-dimethyl-16-ene-19,24-dinorvitamin D3 tert-butyldimethylsilyl ether Edit
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Technology Process of (20R)-1α-[(tert-butyldimethylsilyl)oxy]-2-oxo-22-thia-25-[(methoxymethyl)oxy]-26,27-dimethyl-16-ene-19,24-dinorvitamin D3 tert-butyldimethylsilyl ether

There total 1 articles about (20R)-1α-[(tert-butyldimethylsilyl)oxy]-2-oxo-22-thia-25-[(methoxymethyl)oxy]-26,27-dimethyl-16-ene-19,24-dinorvitamin D3 tert-butyldimethylsilyl ether 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:
diethyl 1-cyanomethylphosphonate; With n-butyllithium; In tetrahydrofuran; hexane; at -40 ℃; for 15h;
(20R)-1α-[(tert-butyldimethylsilyl)oxy]-2-oxo-22-thia-25-[(methoxymethyl)oxy]-26,27-dimethyl-16-ene-19,24-dinorvitamin D3 tert-butyldimethylsilyl ether; In tetrahydrofuran; hexane; at -40 ℃; for 2h; Further stages. Title compound not separated from byproducts.;
DOI:10.1016/j.bmc.2008.05.043
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