A new application about Sodium 2-((2-(stearoyloxy)propanoyl)oxy)propanoate

Interested yet? Keep reading other articles of 25383-99-7, you can contact me at any time and look forward to more communication. Name: Sodium 2-((2-(stearoyloxy)propanoyl)oxy)propanoate.

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 25383-99-7, Name is Sodium 2-((2-(stearoyloxy)propanoyl)oxy)propanoate, molecular formula is C24H43NaO6. In an article, author is Chen, Cheng-yi,once mentioned of 25383-99-7, Name: Sodium 2-((2-(stearoyloxy)propanoyl)oxy)propanoate.

A Divergent and Selective Synthesis of Isomeric Benzoxazoles from a Single N-Cl Imine

A divergent and regioselective synthesis of either 3-substituted benzisoxazoles or 2-substituted benzoxazoles from readily accessible ortho-hydroxyaryl N-H ketimines is described. The reaction proceeds in two distinct pathways through a common N-Cl imine Intermediate: (a) N-O bond formation to form benzisoxazole under anhydrous conditions and (b) NaOCl mediated Beckmann-type rearrangement to form benzoxazole, respectively. The reaction path also depends on the electronic nature of the aromatic ring, with the electron-rich aromatic rings favoring the rearrangement and the electron-deficient rings favoring the N-O bond formation. A Beckmann-type rearrangement mechanism via net [1,2]-aryl migration for the formation of 2-substituted benzoxazole is proposed.

Interested yet? Keep reading other articles of 25383-99-7, you can contact me at any time and look forward to more communication. Name: Sodium 2-((2-(stearoyloxy)propanoyl)oxy)propanoate.

Reference:
Benzisoxazole – Wikipedia,
,Benzisoxazole – an overview | ScienceDirect Topics