Paper
Application of PEG400 in the one-pot synthesis of 7-[4-alkyl- or (hetero)aryl-1H-1,2,3-triazol-1-yl]thieno[3,2-b]pyridines via SNAr and Cu(I)-Catalyzed Azide-Alkyne Cycloaddition and preliminary evaluation of their anti-tumour activity
Published May 28, 2020 · Juliana M. Rodrigues, R. Calhelha, I. Ferreira
Tetrahedron Letters
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Abstract
Abstract hidden due to publisher request; this does not indicate any issues with the research. Click the full text link above to read the abstract and view the original source.
PEG 400 enables the one-pot synthesis of novel anti-tumor compounds, with a 2-ethynylpyridine derivative showing promising anti-tumor activity.
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