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- W2155384500 abstract "Abstract The conjugated dienones 1a , 1c − e , and 1g were synthesized by aldol reaction of cyclohex‐2‐enones 3 with aldehydes or ketones and subsequent elimination. Whereas the acetone adducts could be converted into the desired products 1a / g by treatment with CeCl 3 ·7H 2 O/NaI, the dienones 1c − e were obtained by Appel bromination and dehydrobromination with triethylamine. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004)" @default.
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- W2155384500 date "2004-10-13" @default.
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- W2155384500 title "Synthesis of Novel Bifunctional Michael Acceptors" @default.
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- W2155384500 doi "https://doi.org/10.1002/ejoc.200400419" @default.
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