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- W4383186259 abstract "Abstract Given the prevalence of molecules containing nitro groups in organic synthesis, innovative methods to expand the reactivity of this functional group are of interest in both industrial and academic settings. In this report, a metal‐free intramolecular benzylic sp 3 C−H amination is disclosed using aryl nitro compounds as aryl nitrene precursors. Organosilicon reagent N , N ’‐bis(trimethylsilyl)‐4,4’‐bipyridinylidene (Si‐DHBP) served as an efficient reductant in the transformation, enabling the in situ generation of aryl nitrene species for the direct, metal‐free synthesis of unprotected 2‐arylindolines from the corresponding nitroarene compounds." @default.
- W4383186259 created "2023-07-06" @default.
- W4383186259 creator A5020651212 @default.
- W4383186259 creator A5073099778 @default.
- W4383186259 creator A5073774720 @default.
- W4383186259 creator A5083016936 @default.
- W4383186259 creator A5092401764 @default.
- W4383186259 date "2023-08-21" @default.
- W4383186259 modified "2023-09-29" @default.
- W4383186259 title "Direct Synthesis of Unprotected Indolines Through Intramolecular sp3 C–H Amination Using Nitroarenes as Aryl Nitrene Precursors" @default.
- W4383186259 cites W1598953054 @default.
- W4383186259 cites W1889384145 @default.
- W4383186259 cites W1971698744 @default.
- W4383186259 cites W1973589119 @default.
- W4383186259 cites W1979259658 @default.
- W4383186259 cites W1979923163 @default.
- W4383186259 cites W1988792781 @default.
- W4383186259 cites W1990285287 @default.
- W4383186259 cites W1992259722 @default.
- W4383186259 cites W1995928586 @default.
- W4383186259 cites W2016340075 @default.
- W4383186259 cites W2019871532 @default.
- W4383186259 cites W2022744578 @default.
- W4383186259 cites W2025295426 @default.
- W4383186259 cites W2032663758 @default.
- W4383186259 cites W2037804913 @default.
- W4383186259 cites W2051707977 @default.
- W4383186259 cites W2056660333 @default.
- W4383186259 cites W2058163733 @default.
- W4383186259 cites W2065866227 @default.
- W4383186259 cites W2085624415 @default.
- W4383186259 cites W2090280264 @default.
- W4383186259 cites W2090490503 @default.
- W4383186259 cites W2090763947 @default.
- W4383186259 cites W2091022896 @default.
- W4383186259 cites W2093438374 @default.
- W4383186259 cites W2102945676 @default.
- W4383186259 cites W2115436721 @default.
- W4383186259 cites W2125368188 @default.
- W4383186259 cites W2136566096 @default.
- W4383186259 cites W2137098133 @default.
- W4383186259 cites W2161065172 @default.
- W4383186259 cites W2172032527 @default.
- W4383186259 cites W2302161594 @default.
- W4383186259 cites W2317589856 @default.
- W4383186259 cites W2318355711 @default.
- W4383186259 cites W2329313063 @default.
- W4383186259 cites W2342246777 @default.
- W4383186259 cites W2491347897 @default.
- W4383186259 cites W2513584870 @default.
- W4383186259 cites W2539635553 @default.
- W4383186259 cites W2600131074 @default.
- W4383186259 cites W2621546226 @default.
- W4383186259 cites W2731969445 @default.
- W4383186259 cites W2739347791 @default.
- W4383186259 cites W2739819163 @default.
- W4383186259 cites W2753477215 @default.
- W4383186259 cites W2756405591 @default.
- W4383186259 cites W2767429315 @default.
- W4383186259 cites W2785608634 @default.
- W4383186259 cites W2791521947 @default.
- W4383186259 cites W2800311865 @default.
- W4383186259 cites W2803501277 @default.
- W4383186259 cites W2808915746 @default.
- W4383186259 cites W2885479536 @default.
- W4383186259 cites W2898493890 @default.
- W4383186259 cites W2898795701 @default.
- W4383186259 cites W2906279202 @default.
- W4383186259 cites W2913467458 @default.
- W4383186259 cites W2914520041 @default.
- W4383186259 cites W2922654005 @default.
- W4383186259 cites W2945560990 @default.
- W4383186259 cites W2952042231 @default.
- W4383186259 cites W2958468612 @default.
- W4383186259 cites W2965668787 @default.
- W4383186259 cites W2980626922 @default.
- W4383186259 cites W2991213259 @default.
- W4383186259 cites W3012479598 @default.
- W4383186259 cites W3036309208 @default.
- W4383186259 cites W3047512011 @default.
- W4383186259 cites W3083288364 @default.
- W4383186259 cites W3087728210 @default.
- W4383186259 cites W3111041314 @default.
- W4383186259 cites W3126537536 @default.
- W4383186259 cites W3158361072 @default.
- W4383186259 cites W3162365325 @default.
- W4383186259 cites W3172188452 @default.
- W4383186259 cites W3173820721 @default.
- W4383186259 cites W3178391843 @default.
- W4383186259 cites W3196489570 @default.
- W4383186259 cites W3202936444 @default.
- W4383186259 cites W3205317087 @default.
- W4383186259 cites W3214861290 @default.
- W4383186259 cites W3215348014 @default.
- W4383186259 cites W4206552432 @default.
- W4383186259 cites W4220709343 @default.
- W4383186259 cites W4225279824 @default.
- W4383186259 cites W4290098809 @default.
- W4383186259 cites W4292607405 @default.
- W4383186259 doi "https://doi.org/10.1002/chem.202301978" @default.