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- W2347069125 abstract "A stereoselective vinylogous aldol reaction of N-monosubstituted tetronamides with aldehydes is described. The procedure is simple and scalable, works well with both aromatic and aliphatic aldehydes, and affords mainly the corresponding syn-aldol adducts. In many cases, the latter are obtained essentially free of their anti-isomers (dr > 99 : 1) in high yields (70-90%). Experimental and computational studies suggest that the observed diastereoselectivity arises through anti-syn isomer interconversion, enabled by an iterative retro-aldol/aldol reaction." @default.
- W2347069125 created "2016-06-24" @default.
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- W2347069125 date "2016-01-01" @default.
- W2347069125 modified "2023-10-11" @default.
- W2347069125 title "Thermodynamically driven, syn-selective vinylogous aldol reaction of tetronamides" @default.
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- W2347069125 doi "https://doi.org/10.1039/c6ob00895j" @default.
- W2347069125 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/27163151" @default.
- W2347069125 hasPublicationYear "2016" @default.
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