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- W2607135520 endingPage "613" @default.
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- W2607135520 abstract "From 2-aminonorbornene hydroxamic acids, a simple and efficient method for the preparation of pyrrolo[1,2-a]pyrimidine enantiomers is reported. The synthesis is based on domino ring-closure followed by microwave-induced retro Diels-Alder (RDA) protocols, where the chirality of the desired products is transferred from norbornene derivatives. The stereochemistry of the synthesized compounds was proven by X-ray crystallography. The absolute configuration of the product is determined by the configuration of the starting amino hydroxamic acid." @default.
- W2607135520 created "2017-04-28" @default.
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- W2607135520 date "2017-04-13" @default.
- W2607135520 modified "2023-10-14" @default.
- W2607135520 title "Synthesis of Pyrrolo[1,2-a]pyrimidine Enantiomers via Domino Ring-Closure followed by Retro Diels-Alder Protocol" @default.
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- W2607135520 doi "https://doi.org/10.3390/molecules22040613" @default.
- W2607135520 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6154686" @default.
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