The effect of the change of synthetic route on the product 83435-58-9

From this literature《Synthesis of enantiomerically pure nitronyl nitroxide radicals through chiral pool》,we know some information about this compound(83435-58-9)Safety of Boc-D-Prolinol, but this is not all information, there are many literatures related to this compound(83435-58-9).

Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 83435-58-9, is researched, Molecular C10H19NO3, about Synthesis of enantiomerically pure nitronyl nitroxide radicals through chiral pool, the main research direction is imidazole chiral nitronyl nitroxide radical preparation.Safety of Boc-D-Prolinol.

Two pairs of new optically active nitronyl nitroxides derived from N-Boc-D- or -L-prolinol were described. The synthetic route consists of (1) the synthesis of chiral aryl aldehydes by Mitsunobu reaction, (2) condensation of 2,3-bis(hydroxylamino)-2,3-dimethylbutane with chiral aldehydes to give 1,3-dihydroxyimidazolidines, and (3) finally, subsequent oxidation with aqueous NaIO4 at 0°. These two pairs were specifically designed for further assessing the differences in activity of chiral nitronyl nitroxides and for developing chiral mol. magnetic material by the metal-radical complexes approach.

From this literature《Synthesis of enantiomerically pure nitronyl nitroxide radicals through chiral pool》,we know some information about this compound(83435-58-9)Safety of Boc-D-Prolinol, but this is not all information, there are many literatures related to this compound(83435-58-9).

Reference:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica