Technology Process of [4,5-2H2]-(4S,5R)-2,2-dimethyl-5-(triphenylsilyl)-1,3-dioxolane-4-carbaldehyde
There total 5 articles about [4,5-2H2]-(4S,5R)-2,2-dimethyl-5-(triphenylsilyl)-1,3-dioxolane-4-carbaldehyde which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
(2R,3R)-3-(triphenylsilyl)<2,3-(2)H2>oxiranecarboxaldehyde; acetone;
In
dichloromethane;
at 20 ℃;
for 0.5h;
Molecular sieve;
With
tin(IV) chloride;
In
dichloromethane;
at -78 - -40 ℃;
for 168.5h;
regioselective reaction;
DOI:10.1002/chem.201400296
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: lithium aluminium deuteride
2.1: C11H26O5Ti; L-(+)-diisopropyl tartrate / tert-butyl alcohol
3.1: sulfur trioxide pyridine complex / dimethyl sulfoxide
4.1: dichloromethane / 0.5 h / 20 °C / Molecular sieve
4.2: 168.5 h / -78 - -40 °C
With
lithium aluminium deuteride; L-(+)-diisopropyl tartrate; C11H26O5Ti; sulfur trioxide pyridine complex;
In
dichloromethane; dimethyl sulfoxide; tert-butyl alcohol;
2.1: |Sharpless Asymmetric Epoxidation / 3.1: |Parikh-Doering Oxidation;
DOI:10.1002/chem.201400296
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: C11H26O5Ti; L-(+)-diisopropyl tartrate / tert-butyl alcohol
2.1: sulfur trioxide pyridine complex / dimethyl sulfoxide
3.1: dichloromethane / 0.5 h / 20 °C / Molecular sieve
3.2: 168.5 h / -78 - -40 °C
With
L-(+)-diisopropyl tartrate; C11H26O5Ti; sulfur trioxide pyridine complex;
In
dichloromethane; dimethyl sulfoxide; tert-butyl alcohol;
1.1: |Sharpless Asymmetric Epoxidation / 2.1: |Parikh-Doering Oxidation;
DOI:10.1002/chem.201400296