Stereoselective synthesis of the naturally occurring 2-pyranone dodoneine

Autor:	Juan Murga, Paula Álvarez-Bercedo, Miguel Carda, Eva Falomir, J. Alberto Marco
Rok vydání:	2008
Předmět:	Allylation Stereochemistry Chemistry Organic Chemistry Enantioselective synthesis Total synthesis Asymmetric synthesis Ring (chemistry) Metathesis 5 6-Dihydropyran-2-ones Stereocenter Dodoneine Ring-closing metathesis Oxygen heterocycles Stereoselectivity Physical and Theoretical Chemistry
Zdroj:	Repositori Universitat Jaume I Universitat Jaume I
Popis:	The first total synthesis of the naturally occurring dihydropyranone dodoneine is reported. Asymmetric allylation reactions were used for the stereoselective generation of the two stereogenic centers. The pyranone ring was created by ring-closing metathesis. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5868d0a042efde94f59b332e48c761a7 http://hdl.handle.net/10234/22304 Zobrazit plný text záznamu