Dichotomy in the addition of carbon-centred radicals to ketenedithioacetals

Autor:	Rory Browne, David C. Harrowven
Rok vydání:	1994
Předmět:	chemistry.chemical_classification Bicyclic molecule Chemistry Alkene Radical Organic Chemistry Free-radical reaction chemistry.chemical_element Biochemistry Medicinal chemistry Sulfur Drug Discovery Moiety Carbon
Zdroj:	Tetrahedron Letters. 35:5301-5302
ISSN:	0040-4039
DOI:	10.1016/s0040-4039(00)77090-0
Popis:	Further studies on the addition of carbon centred radicals to ketenedithioacetals have shown that cyclisation may occur to either the sulfur atom or the alkene moiety and that the outcome is governed by the availability of a 5-exo cyclisation process.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::3b136bcf1568d73b1d426e7039b7f6cd https://doi.org/10.1016/s0040-4039(00)77090-0 Zobrazit plný text záznamu