Some scientific research about 2935-35-5

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law. In my other articles, you can also check out more blogs about 2935-35-5. Application In Synthesis of H-Phg-OH.

Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. 2935-35-5, Name is H-Phg-OH, molecular formula is C8H9NO2, belongs to phthalazine compound. In a document, author is Villemin, Elise, introduce the new discover, Application In Synthesis of H-Phg-OH.

The Diels-Alder reaction between diethyl 1-phosphono-1,3-butadiene and cyclic azo dienophiles, such as 4-phenyl- and 4-methyl-1,2,4-triazoline-3,5-diones and phthalazine-1,4-dione gave access to phosphonated bicyclic cycloadducts bearing a N-N junction. Various functionalizations (dihydroxylation, hydrogenation and phosphonic ester deprotection) have been performed with success. The selective N-N cleavage was not possible for the preparation of large heterocycles. The coordination properties of selected bicycles were tested by ESI-HRMS.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law. In my other articles, you can also check out more blogs about 2935-35-5. Application In Synthesis of H-Phg-OH.

Reference:
Phthalazine – Wikipedia,
,Phthalazine | C8H6N2 – PubChem