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• W2953300965 endingPage "10404" @default.
• W2953300965 startingPage "10395" @default.
• W2953300965 abstract "A highly efficient [4 + 2] annulation route to polysubstituted indolizines is described employing a domino Knoevenagel condensation/intramolecular aldol cyclization process as a key step. Construction of pyridine rings in indolizine skeleton was rapidly achieved from several pyrrole-2-carboxaldehydes in good to excellent yields, leading to indolizines with various substituents at the 5, 6, and 7 positions depending on the reacting active methylene partners." @default.
• W2953300965 created "2019-06-27" @default.
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• W2953300965 date "2013-10-08" @default.
• W2953300965 modified "2023-10-18" @default.
• W2953300965 title "Domino Knoevenagel Condensation/Intramolecular Aldol Cyclization Route to Diverse Indolizines with Densely Functionalized Pyridine Units" @default.
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• W2953300965 doi "https://doi.org/10.1021/jo401801j" @default.
• W2953300965 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24067193" @default.
• W2953300965 hasPublicationYear "2013" @default.
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