Self-complementary ABC triblock copolymers via ring-opening metathesis polymerization was written by Bazzi, Hassan S.;Bouffard, Jean;Sleiman, Hanadi F.. And the article was included in Macromolecules in 2003.Application In Synthesis of N-(6-Aminopyridin-2-yl)acetamide This article mentions the following:
The synthesis of the first self-complementary triblock copolymers was carried out by controlled ring-opening polymerization These copolymer possess ordered sequences of complementary mol. recognition blocks and can be synthesized efficiently with deliberate variation of this sequence. Changing the triblock copolymer sequence results in materials with dramatically different self-assembly properties. In the experiment, the researchers used many compounds, for example, N-(6-Aminopyridin-2-yl)acetamide (cas: 1075-62-3Application In Synthesis of N-(6-Aminopyridin-2-yl)acetamide).
N-(6-Aminopyridin-2-yl)acetamide (cas: 1075-62-3) belongs to pyridine derivatives. Pyridine’s the lone pair does not contribute to the aromatic system but importantly influences the chemical properties of pyridine, as it easily supports bond formation via an electrophilic attack. Halopyridines are particularly attractive synthetic building blocks in a variety of cross-coupling methods, including the Suzuki-Miyaura cross-coupling reaction.Application In Synthesis of N-(6-Aminopyridin-2-yl)acetamide