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C35H39N3O6

Base Information Edit
C<sub>35</sub>H<sub>39</sub>N<sub>3</sub>O<sub>6</sub>

Synonyms:C35H39N3O6

Suppliers and Price of C35H39N3O6
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of C35H39N3O6 Edit
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Technology Process of C35H39N3O6

There total 5 articles about C35H39N3O6 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:
H-Asp-OMe; isovaleraldehyde; In methanol; at 20 ℃; for 1h;
(9H-fluoren-9-yl)methyl (S)-1-isocyano-3-phenylpropan-2-ylcarbamate; In methanol; at 20 ℃; optical yield given as %de; diastereoselective reaction;
DOI:10.1016/j.tetlet.2011.08.090
Guidance literature:
Multi-step reaction with 2 steps
1.1: Burgess Reagent / dichloromethane / 60 °C
2.1: methanol / 1 h / 20 °C
2.2: 20 °C
With Burgess Reagent; In methanol; dichloromethane; 2.1: Ugi reaction / 2.2: Ugi reaction;
DOI:10.1016/j.tetlet.2011.08.090
Guidance literature:
Multi-step reaction with 4 steps
1.1: toluene / 65 °C
2.1: dmap; formic acid / dichloromethane / -15 °C
3.1: Burgess Reagent / dichloromethane / 60 °C
4.1: methanol / 1 h / 20 °C
4.2: 20 °C
With dmap; formic acid; Burgess Reagent; In methanol; dichloromethane; toluene; 4.1: Ugi reaction / 4.2: Ugi reaction;
DOI:10.1016/j.tetlet.2011.08.090
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