Matches in SemOpenAlex for { <https://semopenalex.org/work/W3125380625> ?p ?o ?g. }
- W3125380625 endingPage "102" @default.
- W3125380625 startingPage "93" @default.
- W3125380625 abstract "Esterification of N-hydroxyimides to corresponding active esters (N-hydroxyimide esters) is one of the most important organic transformations not only for their importance as versatile intermediates for amides and esters but also their use as coupling partners in various C-S, C-C and C-N coupling reactions. Therefore, there is continuing interest in the development of efficient, practical, and straightforward methodologies for their construction. Nowadays, cross-dehydrogenative coupling reactions, which combine two unmodified C(X)–H (X = heteroatom) bonds for the fabrication of new C(X)–C(X) bonds, are recognized as a fundamental synthetic tool for highly atom-economical synthesis of a wide variety of organic compounds. Along this line, recently, several procedures have been reported for the synthesis of N-hydroxyimide esters through the oxidative C-O coupling of with aldehydes with N-hydroxyimides. This review highlights recent progresses in this interesting research field." @default.
- W3125380625 created "2021-02-01" @default.
- W3125380625 creator A5041966423 @default.
- W3125380625 creator A5047915284 @default.
- W3125380625 creator A5070731071 @default.
- W3125380625 date "2020-11-01" @default.
- W3125380625 modified "2023-10-01" @default.
- W3125380625 title "Cross-dehydrogenative coupling of aldehydes with N-hydroxyimides: An efficient and straightforward route to N-hydroxyimides esters" @default.
- W3125380625 cites W1845038377 @default.
- W3125380625 cites W1970511538 @default.
- W3125380625 cites W2003514383 @default.
- W3125380625 cites W2007114084 @default.
- W3125380625 cites W2039804228 @default.
- W3125380625 cites W2156852908 @default.
- W3125380625 cites W2172370117 @default.
- W3125380625 cites W2261087384 @default.
- W3125380625 cites W2329076747 @default.
- W3125380625 cites W2523337931 @default.
- W3125380625 cites W2523353505 @default.
- W3125380625 cites W2528319008 @default.
- W3125380625 cites W2560605803 @default.
- W3125380625 cites W2598769636 @default.
- W3125380625 cites W2741421341 @default.
- W3125380625 cites W2743785898 @default.
- W3125380625 cites W2749599940 @default.
- W3125380625 cites W2774661728 @default.
- W3125380625 cites W2803483401 @default.
- W3125380625 cites W2888054046 @default.
- W3125380625 cites W2896712007 @default.
- W3125380625 cites W2901321243 @default.
- W3125380625 cites W2914525421 @default.
- W3125380625 cites W2921370988 @default.
- W3125380625 cites W2944758535 @default.
- W3125380625 cites W2947903515 @default.
- W3125380625 cites W2953256175 @default.
- W3125380625 cites W2965921825 @default.
- W3125380625 cites W2974529938 @default.
- W3125380625 cites W3005523682 @default.
- W3125380625 cites W3014138459 @default.
- W3125380625 cites W3036337944 @default.
- W3125380625 doi "https://doi.org/10.22034/jchemlett.2020.120304" @default.
- W3125380625 hasPublicationYear "2020" @default.
- W3125380625 type Work @default.
- W3125380625 sameAs 3125380625 @default.
- W3125380625 citedByCount "3" @default.
- W3125380625 countsByYear W31253806252022 @default.
- W3125380625 crossrefType "journal-article" @default.
- W3125380625 hasAuthorship W3125380625A5041966423 @default.
- W3125380625 hasAuthorship W3125380625A5047915284 @default.
- W3125380625 hasAuthorship W3125380625A5070731071 @default.
- W3125380625 hasConcept C131584629 @default.
- W3125380625 hasConcept C139872579 @default.
- W3125380625 hasConcept C147597530 @default.
- W3125380625 hasConcept C149635348 @default.
- W3125380625 hasConcept C161790260 @default.
- W3125380625 hasConcept C178790620 @default.
- W3125380625 hasConcept C185592680 @default.
- W3125380625 hasConcept C191897082 @default.
- W3125380625 hasConcept C192562407 @default.
- W3125380625 hasConcept C20950531 @default.
- W3125380625 hasConcept C21951064 @default.
- W3125380625 hasConcept C2780378348 @default.
- W3125380625 hasConcept C41008148 @default.
- W3125380625 hasConcept C48424934 @default.
- W3125380625 hasConcept C535685238 @default.
- W3125380625 hasConcept C58312451 @default.
- W3125380625 hasConceptScore W3125380625C131584629 @default.
- W3125380625 hasConceptScore W3125380625C139872579 @default.
- W3125380625 hasConceptScore W3125380625C147597530 @default.
- W3125380625 hasConceptScore W3125380625C149635348 @default.
- W3125380625 hasConceptScore W3125380625C161790260 @default.
- W3125380625 hasConceptScore W3125380625C178790620 @default.
- W3125380625 hasConceptScore W3125380625C185592680 @default.
- W3125380625 hasConceptScore W3125380625C191897082 @default.
- W3125380625 hasConceptScore W3125380625C192562407 @default.
- W3125380625 hasConceptScore W3125380625C20950531 @default.
- W3125380625 hasConceptScore W3125380625C21951064 @default.
- W3125380625 hasConceptScore W3125380625C2780378348 @default.
- W3125380625 hasConceptScore W3125380625C41008148 @default.
- W3125380625 hasConceptScore W3125380625C48424934 @default.
- W3125380625 hasConceptScore W3125380625C535685238 @default.
- W3125380625 hasConceptScore W3125380625C58312451 @default.
- W3125380625 hasIssue "3" @default.
- W3125380625 hasLocation W31253806251 @default.
- W3125380625 hasOpenAccess W3125380625 @default.
- W3125380625 hasPrimaryLocation W31253806251 @default.
- W3125380625 hasRelatedWork W2011251974 @default.
- W3125380625 hasRelatedWork W2094844841 @default.
- W3125380625 hasRelatedWork W2148672780 @default.
- W3125380625 hasRelatedWork W2328884830 @default.
- W3125380625 hasRelatedWork W240724588 @default.
- W3125380625 hasRelatedWork W2418653639 @default.
- W3125380625 hasRelatedWork W2420656103 @default.
- W3125380625 hasRelatedWork W2539765270 @default.
- W3125380625 hasRelatedWork W2562106551 @default.
- W3125380625 hasRelatedWork W2732218143 @default.
- W3125380625 hasRelatedWork W2887050020 @default.
- W3125380625 hasRelatedWork W2890676278 @default.