Matches in SemOpenAlex for { <https://semopenalex.org/work/W2893121412> ?p ?o ?g. }
- W2893121412 endingPage "731" @default.
- W2893121412 startingPage "722" @default.
- W2893121412 abstract "The three-component reaction between alkyl- or arylamines, β-ketoesters and chalcones in refluxing ethanol containing a catalytic amount of Ce(IV) ammonium nitrate allowed the construction of a large library of highly substituted dihydro-m-terphenyl derivatives containing β-alkylamino- or β-arylamino ester moieties. This process generates three new bonds and one ring and proceeds in high atom economy, having two molecules of water as the only side product. Another domino process, in which the original MCR was telescoped with a subsequent aza Michael/retro-aza Michael sequence, allowed the one-pot preparation of a library of compounds with a N-unsubstituted β-aminoester fragment. Finally, to extend the structural diversity of these libraries, we also examined the aromatization of the central ring of our compounds in the presence of dichlorodicyanoquinone. This reaction sequence did not affect the integrity of a stereogenic center belonging to the amino component." @default.
- W2893121412 created "2018-10-05" @default.
- W2893121412 creator A5014165809 @default.
- W2893121412 creator A5037562938 @default.
- W2893121412 creator A5040015253 @default.
- W2893121412 creator A5075353003 @default.
- W2893121412 creator A5076588181 @default.
- W2893121412 creator A5087989828 @default.
- W2893121412 creator A5089419710 @default.
- W2893121412 date "2018-09-24" @default.
- W2893121412 modified "2023-10-03" @default.
- W2893121412 title "Three-Component Synthesis of a Library of <i>m</i>-Terphenyl Derivatives with Embedded β-Aminoester Moieties" @default.
- W2893121412 cites W1482925586 @default.
- W2893121412 cites W1582937646 @default.
- W2893121412 cites W1782839701 @default.
- W2893121412 cites W1935425517 @default.
- W2893121412 cites W1965689120 @default.
- W2893121412 cites W1967608063 @default.
- W2893121412 cites W1968340466 @default.
- W2893121412 cites W1969040606 @default.
- W2893121412 cites W1975000165 @default.
- W2893121412 cites W1975188119 @default.
- W2893121412 cites W1976399396 @default.
- W2893121412 cites W1990944927 @default.
- W2893121412 cites W1993766305 @default.
- W2893121412 cites W1999197232 @default.
- W2893121412 cites W1999618865 @default.
- W2893121412 cites W2005775306 @default.
- W2893121412 cites W2010496573 @default.
- W2893121412 cites W2011464582 @default.
- W2893121412 cites W2025120865 @default.
- W2893121412 cites W2026983176 @default.
- W2893121412 cites W2031008553 @default.
- W2893121412 cites W2044903533 @default.
- W2893121412 cites W2047920115 @default.
- W2893121412 cites W2051248331 @default.
- W2893121412 cites W2057862389 @default.
- W2893121412 cites W2070088384 @default.
- W2893121412 cites W2070238795 @default.
- W2893121412 cites W2071851966 @default.
- W2893121412 cites W2072745650 @default.
- W2893121412 cites W2072940337 @default.
- W2893121412 cites W2073500340 @default.
- W2893121412 cites W2076421149 @default.
- W2893121412 cites W2077372756 @default.
- W2893121412 cites W2079847921 @default.
- W2893121412 cites W2104378433 @default.
- W2893121412 cites W2118595837 @default.
- W2893121412 cites W2121491419 @default.
- W2893121412 cites W2127378043 @default.
- W2893121412 cites W2128365835 @default.
- W2893121412 cites W2138432592 @default.
- W2893121412 cites W2151569601 @default.
- W2893121412 cites W2157740440 @default.
- W2893121412 cites W2172416075 @default.
- W2893121412 cites W2177697332 @default.
- W2893121412 cites W2262775727 @default.
- W2893121412 cites W2315707204 @default.
- W2893121412 cites W2316132249 @default.
- W2893121412 cites W2319555919 @default.
- W2893121412 cites W2319803436 @default.
- W2893121412 cites W2329817156 @default.
- W2893121412 cites W2334376787 @default.
- W2893121412 cites W2343064318 @default.
- W2893121412 cites W2405699446 @default.
- W2893121412 cites W2478964621 @default.
- W2893121412 cites W2518855728 @default.
- W2893121412 cites W2645056440 @default.
- W2893121412 cites W2747475844 @default.
- W2893121412 cites W2912518084 @default.
- W2893121412 cites W2949528061 @default.
- W2893121412 cites W2950517394 @default.
- W2893121412 cites W2951236169 @default.
- W2893121412 cites W2951383172 @default.
- W2893121412 cites W2952218764 @default.
- W2893121412 cites W331404101 @default.
- W2893121412 doi "https://doi.org/10.1021/acscombsci.8b00137" @default.
- W2893121412 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30248256" @default.
- W2893121412 hasPublicationYear "2018" @default.
- W2893121412 type Work @default.
- W2893121412 sameAs 2893121412 @default.
- W2893121412 citedByCount "11" @default.
- W2893121412 countsByYear W28931214122019 @default.
- W2893121412 countsByYear W28931214122020 @default.
- W2893121412 countsByYear W28931214122021 @default.
- W2893121412 countsByYear W28931214122022 @default.
- W2893121412 countsByYear W28931214122023 @default.
- W2893121412 crossrefType "journal-article" @default.
- W2893121412 hasAuthorship W2893121412A5014165809 @default.
- W2893121412 hasAuthorship W2893121412A5037562938 @default.
- W2893121412 hasAuthorship W2893121412A5040015253 @default.
- W2893121412 hasAuthorship W2893121412A5075353003 @default.
- W2893121412 hasAuthorship W2893121412A5076588181 @default.
- W2893121412 hasAuthorship W2893121412A5087989828 @default.
- W2893121412 hasAuthorship W2893121412A5089419710 @default.
- W2893121412 hasConcept C134195300 @default.
- W2893121412 hasConcept C139872579 @default.
- W2893121412 hasConcept C146686406 @default.