Convenient methods for preparing π-conjugated linkers as building blocks for modular chemistry

Autor:	Jiří Kulhánek, Filip Bureš, Miroslav Ludwig
Jazyk:	angličtina
Rok vydání:	2009
Předmět:	boronic acid donor/acceptor linker Sonogashira reaction property tuning push-pull Suzuki–Miyaura reaction Science Organic chemistry QD241-441
Zdroj:	Beilstein Journal of Organic Chemistry, Vol 5, Iss 1, p 11 (2009)
Druh dokumentu:	article
ISSN:	1860-5397 17028744
DOI:	10.3762/bjoc.5.11
Popis:	Simple, straightforward and optimized procedures for preparing extended π-conjugated linkers are described. Either unsubstituted or 4-donor substituted π-linkers bearing a styryl, biphenyl, phenylethenylphenyl, and phenylethynylphenyl π-conjugated backbone are functionalized with boronic pinacol esters as well as with terminal acetylene moieties allowing their further use as building blocks in Suzuki–Miyaura or Sonogashira coupling reactions.
Databáze:	Directory of Open Access Journals
Externí odkaz:	https://doaj.org/article/6b6b1a17028744eea0f7815e8f97dcb6 Zobrazit plný text záznamu View record in DOAJ