Autor:	Neil J. Brown, Keith R. Buszek
Rok vydání:	2014
Předmět:	Indole test Chemistry Organic Chemistry Drug Discovery Diels alder Organic chemistry Regioselectivity Biochemistry Aryne Cycloaddition Article
Zdroj:	Tetrahedron letters. 53(31)
ISSN:	0040-4039
Popis:	We describe the first report of the generation of 6,7-dehydrobenzofuran (6,7-benzofuranyne) from 6,7-dihalobenzofurans via metal-halogen exchange and elimination, in a manner similar to our previous work with 6,7-indole arynes. This benzofuranyne undergoes highly regioselective Diels-Alder cycloadditions with 2-substituted furans.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c394aab8e263fd9f5383f319031ba43 https://pubmed.ncbi.nlm.nih.gov/25278635 Zobrazit plný text záznamu Full Text from ScienceDirect