Cycloaddition of ?-dialkylborylamino-n-heterocycles to cyanamides

Autor:	L. G. Vorontsova, M. N. Bochkareva, M. G. Kurella, M. F. Gordeev, V. A. Dorokhov, Z. K. Dem'yanets
Rok vydání:	1990
Předmět:	chemistry.chemical_compound chemistry Stereochemistry Product (mathematics) Organic chemistry Cyanamide Chelation General Chemistry Crystal structure Cycloaddition
Zdroj:	Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 39:346-350
ISSN:	1573-9171 0568-5230
DOI:	10.1007/bf00960666
Popis:	α-Diisopropylaminopyridine and 2-dipropylborylamino-1-methylbenzimidazole react with cyanamides to give chelate [4+2]-cycloadducts. X-ray crystallography has been used to establish the molecular and crystal structure of the product of the reaction of α-diisopropylaminopyridine and benzoylcyanamide.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::905596fb4b1d4515cedb833293b196e5 https://doi.org/10.1007/bf00960666 Zobrazit plný text záznamu Full text from SpringerLink