Cyclizations of Aminyl Radicals Generated from Substoichiometric Stannane

Autor:	Huimin Zhai, Glenn M. Sammis, Jason G. Wickenden
Rok vydání:	2010
Předmět:	chemistry.chemical_compound chemistry Silylation Organic Chemistry Organic chemistry Tributyltin hydride Medicinal chemistry Stannane Enol
Zdroj:	Synlett. 2010:3035-3038
ISSN:	1437-2096 0936-5214
DOI:	10.1055/s-0030-1259062
Popis:	Substoichiometric amounts of tributyltin hydride were utilized in nitrogen-centered radical cyclizations onto silyl enol ethers for the formation of substituted cyclic imines.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::a260092275297fa1f46367ebed50b866 https://doi.org/10.1055/s-0030-1259062 Zobrazit plný text záznamu