Matches in SemOpenAlex for { <https://semopenalex.org/work/W4313277760> ?p ?o ?g. }
- W4313277760 abstract "A 1,3-carbocarbonation of 2-substituted cyclopropane 1,1-dicarboxylates introduces various saturated or unsaturated carbon residues at the 1- and 3- position of the former three-membered ring. Under copper catalysis, ring-opening attack with a Grignard reagent proceeded smoothly; the intermediate was converted to the final product by reaction with appropriate carbon-based electrophiles under basic conditions. As nucleophiles, Grignard reagents derived from sp3 -, sp2 -, and sp-hybridized carbon residues were successfully employed, whereas various aliphatic bromides and EBX derivatives (for sp moieties) served as electrophiles." @default.
- W4313277760 created "2023-01-06" @default.
- W4313277760 creator A5077903994 @default.
- W4313277760 creator A5079173916 @default.
- W4313277760 creator A5089476171 @default.
- W4313277760 date "2023-02-28" @default.
- W4313277760 modified "2023-09-24" @default.
- W4313277760 title "A Widely Applicable and Versatile Method for the Ring‐Opening 1,3‐Carbocarbonation of Donor‐Acceptor Cyclopropanes" @default.
- W4313277760 cites W1912409625 @default.
- W4313277760 cites W1969487950 @default.
- W4313277760 cites W1997289391 @default.
- W4313277760 cites W1999454465 @default.
- W4313277760 cites W2001190014 @default.
- W4313277760 cites W2010732799 @default.
- W4313277760 cites W2019771325 @default.
- W4313277760 cites W2038573548 @default.
- W4313277760 cites W2046654256 @default.
- W4313277760 cites W2090980622 @default.
- W4313277760 cites W2093592351 @default.
- W4313277760 cites W2110059372 @default.
- W4313277760 cites W2111038935 @default.
- W4313277760 cites W2137041649 @default.
- W4313277760 cites W2145426340 @default.
- W4313277760 cites W2151684584 @default.
- W4313277760 cites W2158239012 @default.
- W4313277760 cites W2162826419 @default.
- W4313277760 cites W2166403448 @default.
- W4313277760 cites W2172195230 @default.
- W4313277760 cites W2247581895 @default.
- W4313277760 cites W2254822416 @default.
- W4313277760 cites W2278969229 @default.
- W4313277760 cites W2300153253 @default.
- W4313277760 cites W2336232079 @default.
- W4313277760 cites W2341154538 @default.
- W4313277760 cites W2479259081 @default.
- W4313277760 cites W2511582635 @default.
- W4313277760 cites W2532305766 @default.
- W4313277760 cites W2565076235 @default.
- W4313277760 cites W2574497537 @default.
- W4313277760 cites W2613643553 @default.
- W4313277760 cites W2623250655 @default.
- W4313277760 cites W2732802163 @default.
- W4313277760 cites W2738328032 @default.
- W4313277760 cites W2791424305 @default.
- W4313277760 cites W2793579924 @default.
- W4313277760 cites W2800778828 @default.
- W4313277760 cites W2888349794 @default.
- W4313277760 cites W2895653909 @default.
- W4313277760 cites W2912301580 @default.
- W4313277760 cites W2955474846 @default.
- W4313277760 cites W2967387521 @default.
- W4313277760 cites W2973649193 @default.
- W4313277760 cites W2995987445 @default.
- W4313277760 cites W2995992275 @default.
- W4313277760 cites W3009384355 @default.
- W4313277760 cites W3029255417 @default.
- W4313277760 cites W3035444085 @default.
- W4313277760 cites W3045922305 @default.
- W4313277760 cites W3047163821 @default.
- W4313277760 cites W3119188029 @default.
- W4313277760 cites W3127656909 @default.
- W4313277760 cites W3135067472 @default.
- W4313277760 cites W3149854973 @default.
- W4313277760 cites W3154474214 @default.
- W4313277760 cites W3181884486 @default.
- W4313277760 cites W3195169289 @default.
- W4313277760 cites W3196415210 @default.
- W4313277760 cites W3200811222 @default.
- W4313277760 cites W4206288976 @default.
- W4313277760 cites W4210335781 @default.
- W4313277760 cites W4210990131 @default.
- W4313277760 cites W4211131255 @default.
- W4313277760 cites W4212798589 @default.
- W4313277760 cites W4223615175 @default.
- W4313277760 cites W4224256645 @default.
- W4313277760 cites W4231247961 @default.
- W4313277760 cites W4233906030 @default.
- W4313277760 cites W4235148753 @default.
- W4313277760 cites W4235764950 @default.
- W4313277760 cites W4239598926 @default.
- W4313277760 cites W4240150718 @default.
- W4313277760 cites W4251785473 @default.
- W4313277760 cites W4285387580 @default.
- W4313277760 doi "https://doi.org/10.1002/chem.202203986" @default.
- W4313277760 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36579656" @default.
- W4313277760 hasPublicationYear "2023" @default.
- W4313277760 type Work @default.
- W4313277760 citedByCount "3" @default.
- W4313277760 countsByYear W43132777602023 @default.
- W4313277760 crossrefType "journal-article" @default.
- W4313277760 hasAuthorship W4313277760A5077903994 @default.
- W4313277760 hasAuthorship W4313277760A5079173916 @default.
- W4313277760 hasAuthorship W4313277760A5089476171 @default.
- W4313277760 hasBestOaLocation W43132777601 @default.
- W4313277760 hasConcept C104779481 @default.
- W4313277760 hasConcept C121332964 @default.
- W4313277760 hasConcept C140205800 @default.
- W4313277760 hasConcept C155647269 @default.
- W4313277760 hasConcept C159985019 @default.
- W4313277760 hasConcept C161790260 @default.