ChemInform Abstract: A Three-Step and Enantioselective Synthesis of (-)-(S)- or (+)-(R)-2-(Furan-3-yl)-3,6-dihydro-2H-pyrans

Autor:	Arrigo Scettri, Margherita De Rosa, Arlette Solladié-Cavallo
Rok vydání:	2010
Předmět:	Terpene chemistry.chemical_compound Manoalide Cacospongionolide B Ring-closing metathesis Chemistry Stereochemistry Furan Enantioselective synthesis General Medicine
Zdroj:	ChemInform. 31
ISSN:	1522-2667 0931-7597
DOI:	10.1002/chin.200024132
Popis:	Enantiomerically enriched (3-furyl)-2-pyran derivatives, key-intermediates in the synthesis of the pharmacophoric pyranofuranone system of the bioactive natural products manoalide and cacospongionolide B, are easily accessible by a rapid sequence involving a chiral allylation and a ring closing metathesis reaction.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::eeaecaec451b0e79851979da0f405331 https://doi.org/10.1002/chin.200024132 Zobrazit plný text záznamu Plný text