Matches in SemOpenAlex for { <https://semopenalex.org/work/W4313304053> ?p ?o ?g. }
- W4313304053 abstract "A novel route to synthesize 1,4-dicarbonyl compounds is described. α,α-Dibromoketones generate zinc enolates through a diethylzinc-mediated halogen-metal exchange and react with α-bromocarbonyl compounds to furnish 1,4-dicarbonyl compounds via a second generation of zinc enolates. This cross-coupling reaction is enabled by the chemoselective formation of zinc enolates from α,α-dibromoketones in the presence of α-bromocarbonyl compounds. Chiral 1,4-dicarbonyl compounds can be obtained via the enantioselective bromination of aldehydes using a chiral secondary amine catalyst and a subsequent cross-coupling reaction between the resulting chiral α-bromoaldehydes and α,α-dibromoacetophenones." @default.
- W4313304053 created "2023-01-06" @default.
- W4313304053 creator A5057205376 @default.
- W4313304053 creator A5072407484 @default.
- W4313304053 date "2023-01-18" @default.
- W4313304053 modified "2023-10-15" @default.
- W4313304053 title "Diethylzinc‐Mediated Cross‐Coupling Reactions between Dibromoketones and Monobromo Carbonyl Compounds" @default.
- W4313304053 cites W1763445961 @default.
- W4313304053 cites W1968095800 @default.
- W4313304053 cites W1980184949 @default.
- W4313304053 cites W1982928176 @default.
- W4313304053 cites W1983514663 @default.
- W4313304053 cites W1984877321 @default.
- W4313304053 cites W1997962389 @default.
- W4313304053 cites W1999718089 @default.
- W4313304053 cites W2006274365 @default.
- W4313304053 cites W2009052001 @default.
- W4313304053 cites W2012767952 @default.
- W4313304053 cites W2013092331 @default.
- W4313304053 cites W2022708431 @default.
- W4313304053 cites W2024834587 @default.
- W4313304053 cites W2031160648 @default.
- W4313304053 cites W2033658892 @default.
- W4313304053 cites W2043275312 @default.
- W4313304053 cites W2043402406 @default.
- W4313304053 cites W2047326581 @default.
- W4313304053 cites W2051822378 @default.
- W4313304053 cites W2053636335 @default.
- W4313304053 cites W2055758035 @default.
- W4313304053 cites W2062476372 @default.
- W4313304053 cites W2063145695 @default.
- W4313304053 cites W2064483090 @default.
- W4313304053 cites W2064675039 @default.
- W4313304053 cites W2071283861 @default.
- W4313304053 cites W2071291147 @default.
- W4313304053 cites W2072793779 @default.
- W4313304053 cites W2086277022 @default.
- W4313304053 cites W2086946482 @default.
- W4313304053 cites W2087527456 @default.
- W4313304053 cites W2090746249 @default.
- W4313304053 cites W2096937981 @default.
- W4313304053 cites W2098337768 @default.
- W4313304053 cites W2101321116 @default.
- W4313304053 cites W2109885290 @default.
- W4313304053 cites W2110838155 @default.
- W4313304053 cites W2118112541 @default.
- W4313304053 cites W2124037933 @default.
- W4313304053 cites W2153700461 @default.
- W4313304053 cites W2154687206 @default.
- W4313304053 cites W2171030833 @default.
- W4313304053 cites W2260865029 @default.
- W4313304053 cites W2316727237 @default.
- W4313304053 cites W2504056772 @default.
- W4313304053 cites W2534638065 @default.
- W4313304053 cites W2733181877 @default.
- W4313304053 cites W2737890673 @default.
- W4313304053 cites W2755403545 @default.
- W4313304053 cites W2760847132 @default.
- W4313304053 cites W2767817928 @default.
- W4313304053 cites W2887055365 @default.
- W4313304053 cites W2901429891 @default.
- W4313304053 cites W2902448274 @default.
- W4313304053 cites W2914565494 @default.
- W4313304053 cites W2949208998 @default.
- W4313304053 cites W2949548980 @default.
- W4313304053 cites W2950116353 @default.
- W4313304053 cites W2950364132 @default.
- W4313304053 cites W2951922604 @default.
- W4313304053 cites W2952478374 @default.
- W4313304053 cites W2953362775 @default.
- W4313304053 cites W2974690394 @default.
- W4313304053 cites W2979296633 @default.
- W4313304053 cites W3006064965 @default.
- W4313304053 cites W3023808359 @default.
- W4313304053 cites W3080336370 @default.
- W4313304053 cites W3108452326 @default.
- W4313304053 cites W3144740287 @default.
- W4313304053 cites W3182372257 @default.
- W4313304053 cites W3201655550 @default.
- W4313304053 cites W3201972348 @default.
- W4313304053 cites W3215594211 @default.
- W4313304053 cites W4205794776 @default.
- W4313304053 cites W4210588651 @default.
- W4313304053 cites W4214837002 @default.
- W4313304053 cites W4224608740 @default.
- W4313304053 cites W4229925151 @default.
- W4313304053 cites W4239338785 @default.
- W4313304053 cites W4241875884 @default.
- W4313304053 cites W4241933495 @default.
- W4313304053 cites W4251429171 @default.
- W4313304053 cites W4251832023 @default.
- W4313304053 cites W4252303581 @default.
- W4313304053 cites W4281713635 @default.
- W4313304053 cites W4281736464 @default.
- W4313304053 cites W4308679412 @default.
- W4313304053 cites W565854973 @default.
- W4313304053 doi "https://doi.org/10.1002/ange.202217496" @default.
- W4313304053 hasPublicationYear "2023" @default.
- W4313304053 type Work @default.
- W4313304053 citedByCount "0" @default.