ChemInform Abstract: Bidentate Lewis Acid Catalyzed Inverse-Electron-Demand Diels-Alder Reaction for the Selective Functionalization of Aldehydes

Autor:	Simon N. Kessler, Hermann A. Wegner, Luca Schweighauser, Daniel Haeussinger, Ina Bodoky
Rok vydání:	2012
Předmět:	chemistry.chemical_compound Denticity chemistry Organic chemistry Surface modification General Medicine Lewis acids and bases Phthalazine Inverse electron-demand Diels–Alder reaction Pyrrolidine Catalysis Naphthalene
Zdroj:	ChemInform. 43
ISSN:	0931-7597
DOI:	10.1002/chin.201245108
Popis:	Enamines, generated in situ from aldehydes and pyrrolidine, undergo inverse-electron demand Diels—Alder with phthalazine (I) to give naphthalene derivatives in low to moderate yields.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::216624d9730d1b571b00ea441fa8529b https://doi.org/10.1002/chin.201245108 Zobrazit plný text záznamu Plný text