INTRAMOLECULAR NITRILE OXIDE CYCLOADDITION ON CHIRAL OLEFINS : A STEREOCONTROLLED APPROACH TO β-KETOL PRECURSORS.
The intramolecular nitrile oxide cycloaddition reaction on (E) or (Z) olefins featuring a sulphur atom along the carbon chain connecting dipole and dipolarophile occurs with a poor to excellent anti stereoselectivity, which is mainly affected by the subst
Annunziata, Rita,Cinquini, Mauro,Cozzi, Franco,Dondio, Gulio,Raimondi, Laura
p. 2369 - 2380
(2007/10/02)
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