New downstream synthetic route of 217192-22-8

Compounds in my other articles are similar to this one((4-(Pyridin-4-yl)phenyl)methanol)Application In Synthesis of (4-(Pyridin-4-yl)phenyl)methanol, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: (4-(Pyridin-4-yl)phenyl)methanol, is researched, Molecular C12H11NO, CAS is 217192-22-8, about Structure-based design, synthesis, and antimicrobial activity of purine derived SAH/MTA nucleosidase inhibitors, the main research direction is adenosylhomocysteine nucleosidase inhibitor design antimicrobial activity; methylthioadenosine nucleosidase inhibitor design antimicrobial activity.Application In Synthesis of (4-(Pyridin-4-yl)phenyl)methanol.

The structure-based design, synthesis, and biol. activity of novel inhibitors of S-adenosyl homocysteine/methylthioadenosine (SAH/MTA) nucleosidase are described. Using 6-substituted purine and deaza purines as the core scaffolds, a systematic and structure guided series of modifications provided low nM inhibitors with broad-spectrum antimicrobial activity.

Compounds in my other articles are similar to this one((4-(Pyridin-4-yl)phenyl)methanol)Application In Synthesis of (4-(Pyridin-4-yl)phenyl)methanol, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.

Reference:
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N2 | ChemSpider