Evaluation of a synthetic route to ε-viniferin based on a new method for the stereoselective preparation of 2,3-diaryl-2,3-dihydrobenzofurans

Autor:	Thomas A. Engler, Bill W. Draney, Gregory A. Gfesser
Rok vydání:	1994
Předmět:	Bicyclic molecule Chemistry Stereochemistry Organic Chemistry Regioselectivity Viniferin Biochemistry Quinone Acid catalysis chemistry.chemical_compound Drug Discovery Organic chemistry Stereoselectivity Lewis acids and bases Phenols
Zdroj:	Tetrahedron Letters. 35:1661-1664
ISSN:	0040-4039
Popis:	Lewis acid-promoted reactions of unsymmetrically substituted (E)-stilbenes with 2-methoxy-1,4-benzoquinones regio- and stereoselectively produce trans 2,3-diaryl-2,3-dihydrobenzofurans.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::55ae60cf0a185b706f62271105b89bc1 https://doi.org/10.1016/0040-4039(94)88313-0 Zobrazit plný text záznamu