Simple exploration of (S)-Propane-1,2-diol

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Electric Literature of 4254-15-3. In my other articles, you can also check out more blogs about 4254-15-3

Electric Literature of 4254-15-3, Chemistry is a science major with cience and engineering. The main research directions are chemical synthesis, new energy materials, nano-ceramics, nano-hybrid composite materials, preparation and modification of special coatings. 4254-15-3, Name is (S)-Propane-1,2-diol,introducing its new discovery.

Regioselective Cyclodehydration of Chiral Diols with Diethoxytriphenylphosphorane, Triphenylphosphine-Tetrachloromethane-Potassium Carbonate, and Triphenylphosphine-Diethyl Azodicarboxylate Reagents. A Comparative Study

The regioselectivity of cyclodehydration of chiral diols has been examined with the reagents diethoxytriphenylphosphorane, triphenylphosphine-tetrachloromethane-potassium carbonate, and triphenylphosphine-diethyl azodicarboxylate. (S)-(+)-Propane-1,2-diol and (R)-(-)-pentane-1,4-diol afford 80-87percent retention of stereochemistry at the chiral carbon in the ether while (S)-(+)-phenylethane-1,2-diol affords essentially racemic styrene oxide with all three reagents.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Electric Literature of 4254-15-3. In my other articles, you can also check out more blogs about 4254-15-3

Reference:
Synthesis and Crystal Structure of a Chiral C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur–nitrogen–oxygen ligand derived from aminothiourea and sodium D-camphor-β-sulfonate