Technology Process of C26H29NO3
There total 3 articles about C26H29NO3 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:
-
Multi-step reaction with 2 steps
1: tetrahydrofuran / 3 h / 0 °C / Inert atmosphere
2: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 2 h / 0 - 20 °C
With
di-isopropyl azodicarboxylate; triphenylphosphine;
In
tetrahydrofuran;
1: |Grignard Reaction / 2: |Mitsunobu Displacement;
DOI:10.1021/jm3008294
- Guidance literature:
-
With
di-isopropyl azodicarboxylate; triphenylphosphine;
In
tetrahydrofuran;
at 0 - 20 ℃;
for 2h;
DOI:10.1021/jm3008294
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: dimethylsulfide borane complex / tetrahydrofuran / 4 h / 0 °C / Inert atmosphere
2.1: dimethyl sulfoxide; oxalyl dichloride / dichloromethane / 0.5 h / -78 °C / Inert atmosphere
2.2: 1 h / -78 °C / Inert atmosphere
3.1: tetrahydrofuran / 3 h / 0 °C / Inert atmosphere
4.1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 2 h / 0 - 20 °C
With
oxalyl dichloride; di-isopropyl azodicarboxylate; dimethylsulfide borane complex; dimethyl sulfoxide; triphenylphosphine;
In
tetrahydrofuran; dichloromethane;
2.1: |Swern Oxidation / 2.2: |Swern Oxidation / 3.1: |Grignard Reaction / 4.1: |Mitsunobu Displacement;
DOI:10.1021/jm3008294