Shape persistent hybrid dendrimers from benzene and triazole via ‘click chemistry’

Autor:	Klaus Müllen, René Stangenberg, David Türp
Rok vydání:	2014
Předmět:	chemistry.chemical_compound chemistry Dendrimer Organic Chemistry Drug Discovery Polymer chemistry Click chemistry Copper catalyzed Triazole Benzene Biochemistry Cycloaddition
Zdroj:	Tetrahedron. 70:3178-3184
ISSN:	0040-4020
DOI:	10.1016/j.tet.2014.03.037
Popis:	Fully aromatic rigid dendrimers have been synthesized at room temperature based on two different ‘click’-reactions: The dendronization was carried out via the copper catalyzed azide–alkyne Huisgen cycloaddition or Diels–Alder cycloaddition, respectively. The feasible combination of both reactions leads to dendrimer hybrids. Stiff aromatic dendrimers, whose highly nitrogen containing scaffolds are solely based on interconnected benzene and triazole rings, were created.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::3f16a1c1dafa5a1fb0d9d66c8a11f52c https://doi.org/10.1016/j.tet.2014.03.037 Zobrazit plný text záznamu Full Text from ScienceDirect