Matches in SemOpenAlex for { <https://semopenalex.org/work/W2087570110> ?p ?o ?g. }
- W2087570110 endingPage "738" @default.
- W2087570110 startingPage "727" @default.
- W2087570110 abstract "Abstract Diels ‐ Alder reactions of the (1 H ‐indol‐3‐yl)‐enacetamides and ‐endiacetamides 1a – d with some carbodieno‐philes and 4‐phenyl‐3 H ‐1,2,4‐triazole‐3,5(4 H )‐dione give rise to the novel amino‐functionalized carbazole; 4 – 6 and 8 ( Scheme 3 ). Ethenetetracarbonitrile reacts with 1b to furnish the Michael ‐type adduct 7 ( Scheme 3 ). Structural aspects of the starting materials 1 , which exhibit above all 3‐vinyl‐1 H ‐indole reactivity, are discussed with regard to the prediction of a Diels ‐ Alder process." @default.
- W2087570110 created "2016-06-24" @default.
- W2087570110 creator A5025834905 @default.
- W2087570110 creator A5037933314 @default.
- W2087570110 creator A5043179678 @default.
- W2087570110 creator A5086564999 @default.
- W2087570110 date "1991-06-19" @default.
- W2087570110 modified "2023-10-03" @default.
- W2087570110 title "Diels-Alder Reactions of (1H-Indol-3-yl)-enacetamides and -endiacetamides: A Selective Access to Acetylamino-Functionalized [b]Annelated Indoles and Carbazoles" @default.
- W2087570110 cites W110983487 @default.
- W2087570110 cites W1966787044 @default.
- W2087570110 cites W1976476074 @default.
- W2087570110 cites W1980045845 @default.
- W2087570110 cites W1991485187 @default.
- W2087570110 cites W1999640625 @default.
- W2087570110 cites W2002288409 @default.
- W2087570110 cites W2013574843 @default.
- W2087570110 cites W2019723070 @default.
- W2087570110 cites W2021191790 @default.
- W2087570110 cites W2023750538 @default.
- W2087570110 cites W2029793661 @default.
- W2087570110 cites W2035858797 @default.
- W2087570110 cites W2047547513 @default.
- W2087570110 cites W2058345288 @default.
- W2087570110 cites W2064129061 @default.
- W2087570110 cites W2068017202 @default.
- W2087570110 cites W2070054030 @default.
- W2087570110 cites W2078965481 @default.
- W2087570110 cites W2084922882 @default.
- W2087570110 cites W2097772127 @default.
- W2087570110 cites W2111485304 @default.
- W2087570110 cites W2134299841 @default.
- W2087570110 cites W2139814845 @default.
- W2087570110 cites W2145374329 @default.
- W2087570110 cites W2318695786 @default.
- W2087570110 cites W2325127680 @default.
- W2087570110 cites W2328158362 @default.
- W2087570110 cites W2949612158 @default.
- W2087570110 cites W2950477022 @default.
- W2087570110 cites W2952644616 @default.
- W2087570110 doi "https://doi.org/10.1002/hlca.19910740406" @default.
- W2087570110 hasPublicationYear "1991" @default.
- W2087570110 type Work @default.
- W2087570110 sameAs 2087570110 @default.
- W2087570110 citedByCount "15" @default.
- W2087570110 crossrefType "journal-article" @default.
- W2087570110 hasAuthorship W2087570110A5025834905 @default.
- W2087570110 hasAuthorship W2087570110A5037933314 @default.
- W2087570110 hasAuthorship W2087570110A5043179678 @default.
- W2087570110 hasAuthorship W2087570110A5086564999 @default.
- W2087570110 hasConcept C108204754 @default.
- W2087570110 hasConcept C112423150 @default.
- W2087570110 hasConcept C142724271 @default.
- W2087570110 hasConcept C155647269 @default.
- W2087570110 hasConcept C161790260 @default.
- W2087570110 hasConcept C178790620 @default.
- W2087570110 hasConcept C185592680 @default.
- W2087570110 hasConcept C192527728 @default.
- W2087570110 hasConcept C204787440 @default.
- W2087570110 hasConcept C24961977 @default.
- W2087570110 hasConcept C2776127813 @default.
- W2087570110 hasConcept C2776910235 @default.
- W2087570110 hasConcept C2779940776 @default.
- W2087570110 hasConcept C71240020 @default.
- W2087570110 hasConcept C71924100 @default.
- W2087570110 hasConceptScore W2087570110C108204754 @default.
- W2087570110 hasConceptScore W2087570110C112423150 @default.
- W2087570110 hasConceptScore W2087570110C142724271 @default.
- W2087570110 hasConceptScore W2087570110C155647269 @default.
- W2087570110 hasConceptScore W2087570110C161790260 @default.
- W2087570110 hasConceptScore W2087570110C178790620 @default.
- W2087570110 hasConceptScore W2087570110C185592680 @default.
- W2087570110 hasConceptScore W2087570110C192527728 @default.
- W2087570110 hasConceptScore W2087570110C204787440 @default.
- W2087570110 hasConceptScore W2087570110C24961977 @default.
- W2087570110 hasConceptScore W2087570110C2776127813 @default.
- W2087570110 hasConceptScore W2087570110C2776910235 @default.
- W2087570110 hasConceptScore W2087570110C2779940776 @default.
- W2087570110 hasConceptScore W2087570110C71240020 @default.
- W2087570110 hasConceptScore W2087570110C71924100 @default.
- W2087570110 hasIssue "4" @default.
- W2087570110 hasLocation W20875701101 @default.
- W2087570110 hasOpenAccess W2087570110 @default.
- W2087570110 hasPrimaryLocation W20875701101 @default.
- W2087570110 hasRelatedWork W1964485806 @default.
- W2087570110 hasRelatedWork W1993432588 @default.
- W2087570110 hasRelatedWork W1998345950 @default.
- W2087570110 hasRelatedWork W2072984946 @default.
- W2087570110 hasRelatedWork W2087570110 @default.
- W2087570110 hasRelatedWork W2126828233 @default.
- W2087570110 hasRelatedWork W2178362803 @default.
- W2087570110 hasRelatedWork W2950438986 @default.
- W2087570110 hasRelatedWork W4313397634 @default.
- W2087570110 hasRelatedWork W4385665248 @default.
- W2087570110 hasVolume "74" @default.
- W2087570110 isParatext "false" @default.
- W2087570110 isRetracted "false" @default.
- W2087570110 magId "2087570110" @default.