The Shocking Revelation of Naphthalen-1-ylboronic acid

These may comprise an expansion of the substrate scope from aromatic and heteroaromatic compounds to other hydrocarbons. If you like, you can also browse other articles about this kind. Thanks for taking the time to read the blog about 13922-41-3, Name: Naphthalen-1-ylboronic acid.

Researchers are common within chemical engineering and are often tasked with creating and developing new chemical techniques, frequently combining other advanced and emerging scientific areas. 13922-41-3, Name is Naphthalen-1-ylboronic acid, SMILES is C1=CC=C2C(=C1)C(=CC=C2)B(O)O, belongs to naphthyridine compound. In a document, author is Sultan, Shaista, introduce the new discover, Name: Naphthalen-1-ylboronic acid.

A procedure for the synthesis of dibenzo-1,7-naphthyridine carboxylate by means of photoredox catalysis has been developed. The reaction features an umpolung reaction of the keto group at the C-3 position and entrapment of the decarbonylation- prone C-2 position of isatin. Additionally, the method is employed to showcase the chemodivergent behavior of isatins in aprotic solvents leading to the synthesis of tryptanthrin derivatives through photoredox catalysis. The reaction is demonstrated to be scalable (up to gram scale) and straightforward in terms of set up.

These may comprise an expansion of the substrate scope from aromatic and heteroaromatic compounds to other hydrocarbons. If you like, you can also browse other articles about this kind. Thanks for taking the time to read the blog about 13922-41-3, Name: Naphthalen-1-ylboronic acid.

Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem