267432-85-9Relevant academic research and scientific papers
Enantioselective diels-alder approach to C-3-oxygenated angucyclinones from (SS)-2-(p-Tolylsulfinyl)-1,4-naphthoquinone
Carreno, M. Carmen,Urbano, Antonio,Vitta, Claudio Di
, p. 906 - 913 (2007/10/03)
Chiral racemic vinylcyclohexenes 2, bearing oxygenated substituents and/or a methyl group at the C-5 position of the cyclohexene ring, were submitted to Diels-Alder reactions with enantiomerically pure (SS)-(2-p- tolylsulfinyl)-1,4-naphthoquinone [(+)-1].
