Palladium(II)-Catalyzed Synthesis of 2-Alkoxytetrahydrofurans from Allylic Alcohols and Vinyl Ethers: Stereospecificity and Catalysis

Autor:	Takuro Imai, Yasufumi Kawamura, Takahiro Hosokawa
Rok vydání:	2006
Předmět:	Allylic rearrangement Catechol Organic Chemistry chemistry.chemical_element Alcohol Medicinal chemistry Catalysis Palladium black chemistry.chemical_compound Stereospecificity chemistry Organic chemistry Allyl alcohol Palladium
Zdroj:	Synlett. 2006:3110-3114
ISSN:	1437-2096 0936-5214
DOI:	10.1055/s-2006-951513
Popis:	The reaction of (E)- or (Z)-cinnamyl alcohol and ethyl vinyl ether with a catalyst consisting of Pd(OAc) 2 , Cu(OAc) 2 , and catechol (1:1:2) under O 2 gives a good yield of(Z)- or (E)-4-benzylidene-2-ethoxytetrahydrofuran, respectively. Similarly, 2-butoxy-4-exomethylenetetrahydrofuran was obtained from allyl alcohol and butyl vinyl ether. In the case of allyl alcohol, however, the catalysis does not proceed well with forming palladium black, if a relatively large amount of Pd(OAc) 2 , such as 0.25 mmol to 0.05 mmol, is used even in a lower palladium/substrate ratio, e.g. 1 mol% concentration of the catalyst.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::f35a2ba76e72c1870aa9aeeef7616607 https://doi.org/10.1055/s-2006-951513 Zobrazit plný text záznamu