(2S,4R)-5-[tert-butoxycarbonylamino-3-(tert-butyldiphenylsiloxy)-phenyl]-4-hydroxy-5-methoxy-3,7-dimethyl-oct-2-en

Base Information

• Chemical Name: (2S,4R)-5-[tert-butoxycarbonylamino-3-(tert-butyldiphenylsiloxy)-phenyl]-4-hydroxy-5-methoxy-3,7-dimethyl-oct-2-en
• CAS No.: 1245571-63-4
• Molecular Formula: C₃₈H₅₃NO₅Si
• Molecular Weight: 631.928

Synonyms:(2S,4R)-5-[tert-butoxycarbonylamino-3-(tert-butyldiphenylsiloxy)-phenyl]-4-hydroxy-5-methoxy-3,7-dimethyl-oct-2-en

Chemical Property of (2S,4R)-5-[tert-butoxycarbonylamino-3-(tert-butyldiphenylsiloxy)-phenyl]-4-hydroxy-5-methoxy-3,7-dimethyl-oct-2-en

Chemical Property:

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Technology Process of (2S,4R)-5-[tert-butoxycarbonylamino-3-(tert-butyldiphenylsiloxy)-phenyl]-4-hydroxy-5-methoxy-3,7-dimethyl-oct-2-en

There total 1 articles about (2S,4R)-5-[tert-butoxycarbonylamino-3-(tert-butyldiphenylsiloxy)-phenyl]-4-hydroxy-5-methoxy-3,7-dimethyl-oct-2-en 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: 33.0%

2-acetoxy-3-butene (6737-11-7) + (2S,4R)-5-[tert-butoxycarbonylamino-3-(tert-butyldiphenylsiloxy)phenyl]-4-methyl-2-methoxy-1-pentanal → (2S,4R)-5-[tert-butoxycarbonylamino-3-(tert-butyldiphenylsiloxy)-phenyl]-4-hydroxy-5-methoxy-3,7-dimethyl-oct-2-en (1245571-63-4)

Guidance literature:

2-acetoxy-3-butene; With tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; In dimethyl sulfoxide; at 20 ℃; for 0.166667h; Inert atmosphere;

With bis(pinacol)diborane; In dimethyl sulfoxide; at 20 - 40 ℃; Inert atmosphere;

(2S,4R)-5-[tert-butoxycarbonylamino-3-(tert-butyldiphenylsiloxy)phenyl]-4-methyl-2-methoxy-1-pentanal; In dimethyl sulfoxide; at 40 ℃; for 20h; stereoselective reaction; Inert atmosphere;

DOI:10.1016/j.tet.2010.04.133

upstream raw materials:

2-acetoxy-3-butene

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