Extended knowledge of 497-25-6

If you are interested in 497-25-6, you can contact me at any time and look forward to more communication. Recommanded Product: Oxazolidin-2-one

Chemistry is traditionally divided into organic and inorganic chemistry. Recommanded Product: Oxazolidin-2-one, The former is the study of compounds containing at least one carbon-hydrogen bonds.In a patent,Which mentioned a new discovery about 497-25-6

The stereochemical course of the oxidation of chiral oxazolidinone-substituted enecarbamates has been studied for singlet oxygen (1O2), dimethyldioxirane (DMD), and m-chloroperbenzoic acid (mCPBA) by examining of the special structural and stereoelectronic features of the enecarbamates. Valuable mechanistic insight into these selective oxidations is gained. Whereas the R1 substituent on the chiral auxiliary is responsible for the steric shielding of the double bond and determines the sense of the pi-facial diastereoselectivity, structural characteristic such as the Z/E configuration and the nature of the R 2 group on the double bond are responsible for the extent of the diastereoselectivity. Stereoelectronic steering by the vinylic nitrogen functionality controls the mode selectivity (ene reaction vs [2+2] cycloaddition) in the case of 1O2.

If you are interested in 497-25-6, you can contact me at any time and look forward to more communication. Recommanded Product: Oxazolidin-2-one

Reference:
Oxazolidine – Wikipedia,
Oxazolidine | C3H271NO – PubChem