More research is needed about 1,3-Diphenylguanidine

Future efforts will undeniably focus on the diversification of the new catalytic transformations. These may comprise an expansion of the substrate scope from aromatic and heteroaromatic compounds to other hydrocarbons. 102-06-7, you can contact me at any time and look forward to more communication. Recommanded Product: 1,3-Diphenylguanidine.

In heterogeneous catalysis, catalysts provide a surface to which reactants bind in a process of adsorption. In homogeneous catalysis, catalysts are in the same phase as the reactants. 102-06-7, Name is 1,3-Diphenylguanidine, molecular formurla is C13H13N3. In a document, author is Martynov, A. V., introducing its new discovery. Recommanded Product: 1,3-Diphenylguanidine.

Synthesis of new heterocycles by oxidation of functionalized cyclic derivatives of bis(2-chlorovinyl) sulfide and selenide

Oxidation of 4-substituted 2,6-bis[(E)-chloromethylidene]thiomorpholine with hydrogen peroxide in a mixture of chloroform with acetic acid afforded the corresponding 4-R-2,6-bis[(E)-chloromethylidene]-thiomorpholine 1-oxide. The results of oxidation of bis[(E)-chloromethylidene]-1,4-dichalcogenanes under analogous conditions depended on the chalcogen nature and its position in the ring. The reaction of 2,6-bis[(E)-chloromethylidene]-1,4-dithiane gave 2,6-bis[(E)-chloromethylidene]-1,4-dithiane-1,1,4,4-tetraone, whereas 3,5-bis[(E)-chloromethylidene]-1,4-thiaselenane-1,1-dione was unexpectedly obtained from 3,5-bis[(E)-chloromethylidene]-1,4-thiaselenane. 2,6-Bis[(E)-chloromethylidene]-1,4-thiaselenane and 2,6-bis[(E)-chloromethylidene]-1,4-diselenane decomposed under the oxidation conditions.

Future efforts will undeniably focus on the diversification of the new catalytic transformations. These may comprise an expansion of the substrate scope from aromatic and heteroaromatic compounds to other hydrocarbons. 102-06-7, you can contact me at any time and look forward to more communication. Recommanded Product: 1,3-Diphenylguanidine.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem