Cycloaddition reaction of vinylketene dithioacetals with generated -benzoquinones

Autor:	S. N. Suryawanshi, Dewan S. Bhakuni, Brijesh Kumar
Rok vydání:	1995
Předmět:	Addition reaction Chemistry Product (mathematics) Yield (chemistry) Organic Chemistry Drug Discovery Organic chemistry Biochemistry Cycloaddition Conjugate
Zdroj:	Tetrahedron Letters. 36:4625-4628
ISSN:	0040-4039
Popis:	The cycloaddition reaction/conjugate addition reaction is effectively controlled by a suitable combination of vinylketene dithioacetals 1 ( a – c ) and in situ generated p -benzoquinones 2 ( a – c ). The reaction of 1c with 2b provided cycloaddition product 3c , while the reaction of 1a with 2b yielded a conjugate addition product 4b in good yield.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::fa39872eca468d3e10a377852807b0aa https://doi.org/10.1016/0040-4039(95)00802-j Zobrazit plný text záznamu Full Text from ScienceDirect