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- W2976611842 endingPage "16031" @default.
- W2976611842 startingPage "16022" @default.
- W2976611842 abstract "Abstract It has been established that a cyclopentadienyl (Cp) Rh III complex with two aryl groups and a pendant amide moiety catalyzes the formal Lossen rearrangement/alkenylation cascade of N ‐pivaloyl heterole carboxamides with internal alkynes, leading to alkenylheteroles. Interestingly, the use of sterically demanding internal alkynes afforded not the alkenylation but the [3+2] annulation products ([5,5]‐fused heteroles). In these reactions, the pendant amide moiety of the CpRh III complex may accelerate the formal Lossen rearrangement. The use of five‐membered heteroles may deter reductive elimination to form strained [5,5]‐fused heteroles; instead, protonation proceeds to give the alkenylation products. Bulky alkyne substituents accelerate the reductive elimination to allow the formation of the [5,5]‐fused heteroles." @default.
- W2976611842 created "2019-10-03" @default.
- W2976611842 creator A5013437976 @default.
- W2976611842 creator A5013619496 @default.
- W2976611842 creator A5090533930 @default.
- W2976611842 date "2019-11-18" @default.
- W2976611842 modified "2023-10-18" @default.
- W2976611842 title "Formal Lossen Rearrangement/Alkenylation or Annulation Cascade of Heterole Carboxamides with Alkynes Catalyzed by CpRh<sup>III</sup> Complexes with Pendant Amides" @default.
- W2976611842 cites W1563323863 @default.
- W2976611842 cites W1910310065 @default.
- W2976611842 cites W1926827464 @default.
- W2976611842 cites W1967897724 @default.
- W2976611842 cites W1974774522 @default.
- W2976611842 cites W1976867032 @default.
- W2976611842 cites W1982826508 @default.
- W2976611842 cites W1983170559 @default.
- W2976611842 cites W1983484395 @default.
- W2976611842 cites W1987587964 @default.
- W2976611842 cites W1989688131 @default.
- W2976611842 cites W2009012040 @default.
- W2976611842 cites W2012315571 @default.
- W2976611842 cites W2015397364 @default.
- W2976611842 cites W2021730225 @default.
- W2976611842 cites W2024520117 @default.
- W2976611842 cites W2030768159 @default.
- W2976611842 cites W2036044855 @default.
- W2976611842 cites W2044192713 @default.
- W2976611842 cites W2047430190 @default.
- W2976611842 cites W2051283356 @default.
- W2976611842 cites W2065578557 @default.
- W2976611842 cites W2067433167 @default.
- W2976611842 cites W2072356342 @default.
- W2976611842 cites W2078571783 @default.
- W2976611842 cites W2078874771 @default.
- W2976611842 cites W2102529897 @default.
- W2976611842 cites W2104742517 @default.
- W2976611842 cites W2118797748 @default.
- W2976611842 cites W2121041004 @default.
- W2976611842 cites W2122996218 @default.
- W2976611842 cites W2124066328 @default.
- W2976611842 cites W2124712143 @default.
- W2976611842 cites W2127454335 @default.
- W2976611842 cites W2133275647 @default.
- W2976611842 cites W2139376946 @default.
- W2976611842 cites W2144448700 @default.
- W2976611842 cites W2150911938 @default.
- W2976611842 cites W2156974767 @default.
- W2976611842 cites W2162721076 @default.
- W2976611842 cites W2169694238 @default.
- W2976611842 cites W2176712993 @default.
- W2976611842 cites W2218281080 @default.
- W2976611842 cites W2265223404 @default.
- W2976611842 cites W2279524934 @default.
- W2976611842 cites W2302508466 @default.
- W2976611842 cites W2315356905 @default.
- W2976611842 cites W2317771072 @default.
- W2976611842 cites W2318193487 @default.
- W2976611842 cites W2321928492 @default.
- W2976611842 cites W2323495415 @default.
- W2976611842 cites W2323997881 @default.
- W2976611842 cites W2328859337 @default.
- W2976611842 cites W2331297548 @default.
- W2976611842 cites W2339051409 @default.
- W2976611842 cites W2340442100 @default.
- W2976611842 cites W2344127674 @default.
- W2976611842 cites W2394806712 @default.
- W2976611842 cites W2401290240 @default.
- W2976611842 cites W2460959534 @default.
- W2976611842 cites W2466129103 @default.
- W2976611842 cites W2476721801 @default.
- W2976611842 cites W2502936635 @default.
- W2976611842 cites W2504203152 @default.
- W2976611842 cites W2514655085 @default.
- W2976611842 cites W2521144274 @default.
- W2976611842 cites W2569294683 @default.
- W2976611842 cites W2579671295 @default.
- W2976611842 cites W2580735059 @default.
- W2976611842 cites W2582614442 @default.
- W2976611842 cites W2589065087 @default.
- W2976611842 cites W2591328444 @default.
- W2976611842 cites W2601598271 @default.
- W2976611842 cites W2615943424 @default.
- W2976611842 cites W2757603095 @default.
- W2976611842 cites W2763246001 @default.
- W2976611842 cites W2767739802 @default.
- W2976611842 cites W2776710466 @default.
- W2976611842 cites W2783950304 @default.
- W2976611842 cites W2789454723 @default.
- W2976611842 cites W2791304971 @default.
- W2976611842 cites W2791374549 @default.
- W2976611842 cites W2793241988 @default.
- W2976611842 cites W2796071904 @default.
- W2976611842 cites W2796526806 @default.
- W2976611842 cites W2800173575 @default.
- W2976611842 cites W2800409626 @default.
- W2976611842 cites W2804536824 @default.
- W2976611842 cites W2883096078 @default.
- W2976611842 cites W2883408915 @default.