New research progress on 4254-15-3 in 2021. In classical electrochemical theory, both the electron transfer rate and the adsorption of reactants at the electrode control the electrochemical reaction. COA of Formula: C3H8O2, The former is the study of compounds containing at least one carbon-hydrogen bonds.In a patent，Which mentioned a new discovery about 4254-15-3
Enantiomerically pure cyclic chiral sulfite (S)-7 (trans stereochemistry) has been easily obtained in two steps from (S)-ethyl lactate.This compound was found to react cleanly with many organometallics to give crystalline sulfinates with high regioselectivity (>90:10).Addition of a second organometallic transforms the purified sulfinate in excellent yield into a chiral sulfoxide (100percent ee) of predictable absolute configuration.The mechanism and scope of this approach are discussed.This method completes the various other methdos of preparation of chiral sulfoxides and is especially convenient for the preparation of tert-butyl sulfoxides.Examples for the synthesis of many chiral tert-butyl sulfoxides are given.The case of chiral sulfites derived from a C2 diol or of a chiral monoalcohol is also proposed as a route to chiral sulfinates, and some promising preliminary results have been obtained.The general main route to obtain chiral sulfoxides from sulfites are also discussed.
By the way, COA of Formula: C3H8O2, if you are interested in learning more fun chemistry with your kids, get your hands into one chemistry set now, and start enjoying the best part of chemistry: experiments 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