A new reaction of acetylenes with terminal ternary bonds

Autor:	I. L. Kotlyarevskii, Mark S. Shvartsberg, A. N. Kozhevnikova, V. N. Andrievskii
Rok vydání:	1970
Předmět:	Aryl Condensation Halide chemistry.chemical_element General Chemistry Triple bond Copper Metal chemistry.chemical_compound Acetylene chemistry visual_art Polymer chemistry visual_art.visual_art_medium Organic chemistry Ternary operation
Zdroj:	Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 19:1079-1082
ISSN:	1573-9171 0568-5230
DOI:	10.1007/bf01084322
Popis:	1. The authors have developed a new method of direct introduction of acetylene substituents into aromatic and heteroaromatic rings, consisting in single stage condensation of acetylene with terminal triple bonds with aryl and hetaryl halides in the presence of bases and metallic copper. 2. The use of acetals of tertiary acetylene alcohols in condensation is a method of obtaining monosubsituted aryl and hetaryl acetylenes.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::f0e02527305aa2b65f8b48c4a97307c3 https://doi.org/10.1007/bf01084322 Zobrazit plný text záznamu Full text from SpringerLink