Diels–Alder Reactions of 2-Vinylindoles with Cyclic Dienophiles: Synthesis of [c]-Annulated Tetrahydrocarbazoles

Autor:	Giorgio Abbiati, Valentina Pirovano, Monica Dell'Acqua, Elisabetta Rossi, Mara Giordano, Diego Facoetti
Rok vydání:	2012
Předmět:	chemistry.chemical_compound Chemistry Organic Chemistry Diels alder Lewis acids and bases Carbonyl group Medicinal chemistry Diels–Alder reaction
Zdroj:	Synlett. 23:2913-2918
ISSN:	1437-2096 0936-5214
DOI:	10.1055/s-0032-1317588
Popis:	Diels–Alder reactions of 2-vinylindoles with cyclic carbo- and heterodienophiles, in the presence of suitable Lewis acids, led to uncommon [ c ]-carbo- and furoannulated tetrahydrocarbazoles. The obtained compounds encompass a carbonyl group in an angular position, suitable for further transformations, and represent useful intermediates for the synthesis of more complex structures.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::67bcd4e199cf823bdd17bfacfe98f4d1 https://doi.org/10.1055/s-0032-1317588 Zobrazit plný text záznamu