Matches in SemOpenAlex for { <https://semopenalex.org/work/W2952181837> ?p ?o ?g. }
Showing items 1 to 47 of
47
with 100 items per page.
- W2952181837 abstract "A new and efficient strategy for the synthesis of substituted quinolines via electrophilic cyclization is developed. The intramolecular cyclization of 1-azido-2-(2-propynyl)benzene 1 proceeds smoothly in the presence of electrophilic reagents (I2, Br2, ICl, NBS, NIS, and HNTf2) in CH3NO2 at room temperature or in the presence of catalytic amounts of AuCl3/AgNTf2 in THF at 100 °C to afford the corresponding quinolines 2 in good to high yields. In the case of the electrophilic reagents, E of 2 is either I, Br, or H, depending on the reagent type, while E of 2 is H in the case of the electrophilic catalyst." @default.
- W2952181837 created "2019-06-27" @default.
- W2952181837 creator A5036847215 @default.
- W2952181837 creator A5081669336 @default.
- W2952181837 creator A5084597243 @default.
- W2952181837 date "2010-06-08" @default.
- W2952181837 modified "2023-09-24" @default.
- W2952181837 title "ChemInform Abstract: A Method for the Synthesis of Substituted Quinolines via Electrophilic Cyclization of 1-Azido-2-(2-propynyl)benzene." @default.
- W2952181837 cites W1982027321 @default.
- W2952181837 doi "https://doi.org/10.1002/chin.201023141" @default.
- W2952181837 hasPublicationYear "2010" @default.
- W2952181837 type Work @default.
- W2952181837 sameAs 2952181837 @default.
- W2952181837 citedByCount "0" @default.
- W2952181837 crossrefType "journal-article" @default.
- W2952181837 hasAuthorship W2952181837A5036847215 @default.
- W2952181837 hasAuthorship W2952181837A5081669336 @default.
- W2952181837 hasAuthorship W2952181837A5084597243 @default.
- W2952181837 hasConcept C155647269 @default.
- W2952181837 hasConcept C161790260 @default.
- W2952181837 hasConcept C178790620 @default.
- W2952181837 hasConcept C185592680 @default.
- W2952181837 hasConcept C21951064 @default.
- W2952181837 hasConcept C2775982679 @default.
- W2952181837 hasConcept C2777691172 @default.
- W2952181837 hasConcept C2778824931 @default.
- W2952181837 hasConcept C40875361 @default.
- W2952181837 hasConcept C50027330 @default.
- W2952181837 hasConcept C75079739 @default.
- W2952181837 hasConceptScore W2952181837C155647269 @default.
- W2952181837 hasConceptScore W2952181837C161790260 @default.
- W2952181837 hasConceptScore W2952181837C178790620 @default.
- W2952181837 hasConceptScore W2952181837C185592680 @default.
- W2952181837 hasConceptScore W2952181837C21951064 @default.
- W2952181837 hasConceptScore W2952181837C2775982679 @default.
- W2952181837 hasConceptScore W2952181837C2777691172 @default.
- W2952181837 hasConceptScore W2952181837C2778824931 @default.
- W2952181837 hasConceptScore W2952181837C40875361 @default.
- W2952181837 hasConceptScore W2952181837C50027330 @default.
- W2952181837 hasConceptScore W2952181837C75079739 @default.
- W2952181837 hasLocation W29521818371 @default.
- W2952181837 hasOpenAccess W2952181837 @default.
- W2952181837 hasPrimaryLocation W29521818371 @default.
- W2952181837 isParatext "false" @default.
- W2952181837 isRetracted "false" @default.
- W2952181837 magId "2952181837" @default.
- W2952181837 workType "article" @default.