Matches in SemOpenAlex for { <https://semopenalex.org/work/W2162223650> ?p ?o ?g. }
Showing items 1 to 63 of
63
with 100 items per page.
- W2162223650 endingPage "1484" @default.
- W2162223650 startingPage "1480" @default.
- W2162223650 abstract "3-Aroylindoles have been prepared via copper-catalyzed cyclization of N-(2-iodoaryl)enaminones, readily available from 2-iodoanilines and α,β-ynones. The reaction tolerates a variety of useful functionalities including ether, keto, cyano, bromo, and chloro substituents. This indole synthesis can also be carried out from 2-iodoanilines and α,β-ynones through a sequential process that omits the isolation of enaminone intermediates." @default.
- W2162223650 created "2016-06-24" @default.
- W2162223650 creator A5026316926 @default.
- W2162223650 creator A5035145579 @default.
- W2162223650 creator A5054903963 @default.
- W2162223650 creator A5073432532 @default.
- W2162223650 creator A5085354233 @default.
- W2162223650 date "2009-05-04" @default.
- W2162223650 modified "2023-10-11" @default.
- W2162223650 title "3-Aroylindoles via Copper-Catalyzed Cyclization of <i>N</i>-(2-Iodoaryl)enaminones" @default.
- W2162223650 doi "https://doi.org/10.1055/s-0029-1216742" @default.
- W2162223650 hasPublicationYear "2009" @default.
- W2162223650 type Work @default.
- W2162223650 sameAs 2162223650 @default.
- W2162223650 citedByCount "8" @default.
- W2162223650 countsByYear W21622236502017 @default.
- W2162223650 countsByYear W21622236502018 @default.
- W2162223650 countsByYear W21622236502019 @default.
- W2162223650 countsByYear W21622236502021 @default.
- W2162223650 countsByYear W21622236502023 @default.
- W2162223650 crossrefType "journal-article" @default.
- W2162223650 hasAuthorship W2162223650A5026316926 @default.
- W2162223650 hasAuthorship W2162223650A5035145579 @default.
- W2162223650 hasAuthorship W2162223650A5054903963 @default.
- W2162223650 hasAuthorship W2162223650A5073432532 @default.
- W2162223650 hasAuthorship W2162223650A5085354233 @default.
- W2162223650 hasConcept C161790260 @default.
- W2162223650 hasConcept C178790620 @default.
- W2162223650 hasConcept C185592680 @default.
- W2162223650 hasConcept C192527728 @default.
- W2162223650 hasConcept C21951064 @default.
- W2162223650 hasConcept C2780407432 @default.
- W2162223650 hasConcept C2991944050 @default.
- W2162223650 hasConcept C544778455 @default.
- W2162223650 hasConceptScore W2162223650C161790260 @default.
- W2162223650 hasConceptScore W2162223650C178790620 @default.
- W2162223650 hasConceptScore W2162223650C185592680 @default.
- W2162223650 hasConceptScore W2162223650C192527728 @default.
- W2162223650 hasConceptScore W2162223650C21951064 @default.
- W2162223650 hasConceptScore W2162223650C2780407432 @default.
- W2162223650 hasConceptScore W2162223650C2991944050 @default.
- W2162223650 hasConceptScore W2162223650C544778455 @default.
- W2162223650 hasIssue "09" @default.
- W2162223650 hasLocation W21622236501 @default.
- W2162223650 hasOpenAccess W2162223650 @default.
- W2162223650 hasPrimaryLocation W21622236501 @default.
- W2162223650 hasRelatedWork W2013711494 @default.
- W2162223650 hasRelatedWork W2019068998 @default.
- W2162223650 hasRelatedWork W2319395258 @default.
- W2162223650 hasRelatedWork W2349568673 @default.
- W2162223650 hasRelatedWork W2385488077 @default.
- W2162223650 hasRelatedWork W2908070201 @default.
- W2162223650 hasRelatedWork W2951348219 @default.
- W2162223650 hasRelatedWork W2951531801 @default.
- W2162223650 hasRelatedWork W4226324215 @default.
- W2162223650 hasRelatedWork W3083343956 @default.
- W2162223650 hasVolume "2009" @default.
- W2162223650 isParatext "false" @default.
- W2162223650 isRetracted "false" @default.
- W2162223650 magId "2162223650" @default.
- W2162223650 workType "article" @default.