ChemInform Abstract: Selective and Efficient Access to ortho, meta and para Ring- Substituted Phenylacetylene Derivatives R-(CC-C6H4)x-Y (Y: H, NO2, CN, I, NH2)

Autor:	Sandrine Cabioch, Pierre H. Dixneuf, Jiri Vohlidal, Olivier Lavastre
Rok vydání:	2010
Předmět:	inorganic chemicals chemistry.chemical_compound Phenylacetylene Chemistry Sandmeyer reaction heterocyclic compounds General Medicine Bond formation Ring (chemistry) Medicinal chemistry
Zdroj:	ChemInform. 28
ISSN:	0931-7597
DOI:	10.1002/chin.199739095
Popis:	ortho, meta and para isomers of iodo and amino ring-substituted phenylacetylene as well as rod-like arylacetylene derivatives were prepared by a simple synthetic route involving three consecutive reactions: the palladium-catalysed carbon-carbon bond formation, the Sandmeyer reaction and the desilylation of the protected trimethylsilylalkynes.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::5b050bbb5f5cb803b01ca02bf7082a2c https://doi.org/10.1002/chin.199739095 Zobrazit plný text záznamu Plný text