134387-60-3Relevant articles and documents
CYCLOADDITION OF 1-METHOXY-3-TRIMETHYLSILYLOXYBUTADIENE WITH HALOGENATED CARBONYL COMPOUNDS
Sera, Akira,Iwasaki, Yasuji,Umeda, Michio,Itoh, Kuniaki
, p. 273 - 278 (1991)
Cycloadditions of 1-methoxy-3-trimethylsilyloxy-1,3-butadiene (1) with halogenated carbonyl compounds (2) yielded corresponding substituted tetrahydro- and/or dihydropyran-4-ones (3 and/or 4).Lewis acids were found to be effective as catalysts.Reactions with less reactive carbonyl compounds (2c,d) afforded p-hydroxyacetophenone (5) produced by cyclodimerization of 1.Stereochemistry of the adducts was deduced by 1H nmr spectroscopy.