ChemInform Abstract: The Homoconjugated Electron-Releasing Carbonyl Group of 1- Methylbicyclo(2.2.1)hept-5-en-2-one. Regioselective Syntheses of 5- Chloro- and 6-Chloro-1-methylbicyclo(2.2.1)hept-5-en-2-one

Autor:	Pierre Vogel, Philippe Kernen
Rok vydání:	2010
Předmět:	chemistry.chemical_compound Chemistry Regioselectivity General Medicine Medicinal chemistry Carbonyl group Adduct
Zdroj:	ChemInform. 24
ISSN:	0931-7597
DOI:	10.1002/chin.199352160
Popis:	Syntheses of (+/-)-2-exo-cyano-1-methyl-7-oxabicyclo[2.2.1]hept-5-en-2-endo-yl acetate (1) and of (+/-)-1-methyl-7-oxabicyclo[2.2.1]hept-5-en-2-one (2) are reported. The additon of PhSeCl to 1 afforded (+/-)-5-endo-chloro-2-exo-cyano-1-methyl-6-exo-(phenylselenenyl)-7-oxabi cyclo[2.2.1]hept-2-endo-yl acetate (6), whereas 2 added to PhSeCl with the opposite regioselectivity giving (+/-)-6-endo-chloro-1-methyl-5-exo-(phenylselenenyl)-7-oxabicyclo[2.2.1] heptan-2-one (7). These adducts were converted into 5-chloro-1-methyl-7-oxabicyclo[2.2.1]hept-5-en-2-one (9) and 6-chloro-1-methyl-7-oxabicyclo[2.2.1]hept-5-en-2-one (10), respectively.
Databáze:	OpenAIRE
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