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- W2774699639 abstract "We have unfolded a convenient and mild protocol for the synthesis of diaryl ketones via Pd‐ NHC catalysed carbonylative Suzuki coupling reaction. Notably, this method offers advantages like no use of toxic CO gas, shorter reaction time, high yield, and broad substrate scope. Several sensitive functional groups (like‐COMe, ‐COOMe, ‐F, ‐Cl, ‐Br, ‐NH 2 , ‐CN) are well tolerated in this reaction. In addition, we have also demonstrated a new efficient route for the synthesis of biologically active and pharmaceutically important 2‐substituted 3‐Aroylquinolin‐4(1 H )‐ones and acridone scaffolds." @default.
- W2774699639 created "2017-12-22" @default.
- W2774699639 creator A5008849991 @default.
- W2774699639 creator A5053769721 @default.
- W2774699639 creator A5078196422 @default.
- W2774699639 date "2017-12-08" @default.
- W2774699639 modified "2023-10-03" @default.
- W2774699639 title "Pd‐NHC catalysed Carbonylative Suzuki coupling reaction and its application towards the synthesis of biologically active 3‐aroylquinolin‐4 (1<i>H</i>)‐one and acridone scaffolds" @default.
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- W2774699639 doi "https://doi.org/10.1002/aoc.4173" @default.
- W2774699639 hasPublicationYear "2017" @default.
- W2774699639 type Work @default.