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• W2901233264 endingPage "93" @default.
• W2901233264 startingPage "76" @default.
• W2901233264 abstract "The amide functional group is commonly found in peptides, proteins, pharmaceutical compounds, natural products, and polymers. The synthesis of amides is typically performed by using classical approaches that involve the reaction between a carboxylic acid and an amine in the presence of an activator. Amides are thought to be an inert functional group, because they are unsusceptible to nucleophile attack, owing to their low electrophilicity. The reason for this resistance is clear: the resonance stability of the amide bond. However, transition metal catalysis can circumvent this stability by selectively rupturing the N-C bond of the amide, thereby facilitating further cross-coupling or other reactions. In this Focus Review, we discuss the recent advances in this area and present a summary of methods that have been developed for activating the amide N-C bond by using precious and non-precious metals." @default.
• W2901233264 created "2018-11-29" @default.
• W2901233264 creator A5025268103 @default.
• W2901233264 creator A5084407502 @default.
• W2901233264 date "2018-12-06" @default.
• W2901233264 modified "2023-10-12" @default.
• W2901233264 title "Recent Advances in the Metal-Catalyzed Activation of Amide Bonds" @default.
• W2901233264 cites W1159743676 @default.
• W2901233264 cites W1884894777 @default.
• W2901233264 cites W1929109117 @default.
• W2901233264 cites W1943008936 @default.
• W2901233264 cites W1981249378 @default.
• W2901233264 cites W1988533616 @default.
• W2901233264 cites W1989531234 @default.
• W2901233264 cites W2006180951 @default.
• W2901233264 cites W2006226504 @default.
• W2901233264 cites W2012804498 @default.
• W2901233264 cites W2023912170 @default.
• W2901233264 cites W2031762952 @default.
• W2901233264 cites W2045148055 @default.
• W2901233264 cites W2047509345 @default.
• W2901233264 cites W2051760313 @default.
• W2901233264 cites W2052907531 @default.
• W2901233264 cites W2061084170 @default.
• W2901233264 cites W2065978375 @default.
• W2901233264 cites W2080461000 @default.
• W2901233264 cites W2080691320 @default.
• W2901233264 cites W2083482264 @default.
• W2901233264 cites W2094871139 @default.
• W2901233264 cites W2111729898 @default.
• W2901233264 cites W2120859438 @default.
• W2901233264 cites W2141892726 @default.
• W2901233264 cites W2167998946 @default.
• W2901233264 cites W2198344477 @default.
• W2901233264 cites W2234167111 @default.
• W2901233264 cites W2237104335 @default.
• W2901233264 cites W2257114829 @default.
• W2901233264 cites W2273124147 @default.
• W2901233264 cites W2286518416 @default.
• W2901233264 cites W2324007162 @default.
• W2901233264 cites W2331170245 @default.
• W2901233264 cites W2338100037 @default.
• W2901233264 cites W2341379833 @default.
• W2901233264 cites W2345809476 @default.
• W2901233264 cites W2398305159 @default.
• W2901233264 cites W2424593201 @default.
• W2901233264 cites W2461992628 @default.
• W2901233264 cites W2494013278 @default.
• W2901233264 cites W2499867668 @default.
• W2901233264 cites W2502380854 @default.
• W2901233264 cites W2503574200 @default.
• W2901233264 cites W2512639925 @default.
• W2901233264 cites W2515721730 @default.
• W2901233264 cites W2529166689 @default.
• W2901233264 cites W2529598762 @default.
• W2901233264 cites W2546641655 @default.
• W2901233264 cites W2548072374 @default.
• W2901233264 cites W2549417026 @default.
• W2901233264 cites W2556601502 @default.
• W2901233264 cites W2570055317 @default.
• W2901233264 cites W2588833167 @default.
• W2901233264 cites W2598646131 @default.
• W2901233264 cites W2599793474 @default.
• W2901233264 cites W2603073582 @default.
• W2901233264 cites W2605351325 @default.
• W2901233264 cites W2605413397 @default.
• W2901233264 cites W2610550558 @default.
• W2901233264 cites W2611117591 @default.
• W2901233264 cites W2611737529 @default.
• W2901233264 cites W2621292383 @default.
• W2901233264 cites W2622046301 @default.
• W2901233264 cites W2622610048 @default.
• W2901233264 cites W2623110373 @default.
• W2901233264 cites W2623257910 @default.
• W2901233264 cites W2667976850 @default.
• W2901233264 cites W2724551730 @default.
• W2901233264 cites W2725561759 @default.
• W2901233264 cites W2732218143 @default.
• W2901233264 cites W2734434253 @default.
• W2901233264 cites W2735946225 @default.
• W2901233264 cites W2741011467 @default.
• W2901233264 cites W2742693127 @default.
• W2901233264 cites W2745745497 @default.
• W2901233264 cites W2748612127 @default.
• W2901233264 cites W2754696738 @default.
• W2901233264 cites W2754941572 @default.
• W2901233264 cites W2756405591 @default.
• W2901233264 cites W2764150248 @default.
• W2901233264 cites W2768694856 @default.
• W2901233264 cites W2770263884 @default.
• W2901233264 cites W2771189878 @default.
• W2901233264 cites W2778903699 @default.
• W2901233264 cites W2783377258 @default.
• W2901233264 cites W2785191358 @default.
• W2901233264 cites W2788051333 @default.
• W2901233264 cites W2793549199 @default.
• W2901233264 cites W2795409723 @default.
• W2901233264 cites W2795957213 @default.

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