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- W2020201840 abstract "Catalytic and highly enantioselective Diels−Alder reaction of cyclic and acyclic dienes with α-phthalimidoacroleins provides cyclic α-quaternary α-amino acid precursors. The conformationally flexible chiral ammonium salt of H-l-Phe-l-Leu-N(CH2CH2)2-reduced triamine with pentafluorobenzensulfonic acid is very effective as an asymmetric catalyst for the Diels−Alder reaction." @default.
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- W2020201840 title "Organocatalytic Enantioselective Diels−Alder Reaction of Dienes with α-(<i>N</i>,<i>N</i>-Diacylamino)acroleins" @default.
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