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- W2733156789 endingPage "8257" @default.
- W2733156789 startingPage "8251" @default.
- W2733156789 abstract "A new sequential approach for 2-vinylanilines utilizing aryl carboxylic acids as stable, inexpensive and widely available arylating reagents is described. Employing a Pd-POVs catalyst system, this protocol is not only overcoming the restriction barrier of decarboxylative coupling to ortho-substituted substrates, but also provides site-special to create new C(sp2)-N and C(sp2)-C(sp2) bonds. Mechanistic experiments suggest the cleavage of C(sp2)-COOH gives priority to C(sp2)-X bond in this reaction." @default.
- W2733156789 created "2017-07-14" @default.
- W2733156789 creator A5013000511 @default.
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- W2733156789 creator A5070412796 @default.
- W2733156789 creator A5082429626 @default.
- W2733156789 date "2017-07-14" @default.
- W2733156789 modified "2023-10-17" @default.
- W2733156789 title "Regioselective Synthesis of 2-Vinylanilines Using <i>O</i>-aroyloxycarba-mates by Sequential Decarboxylation/Amination/Heck Reaction" @default.
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- W2733156789 doi "https://doi.org/10.1021/acs.joc.7b01020" @default.
- W2733156789 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/28664735" @default.
- W2733156789 hasPublicationYear "2017" @default.
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