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- W2951839861 endingPage "912" @default.
- W2951839861 startingPage "907" @default.
- W2951839861 abstract "A simple one-pot two-step reaction comprising an Ugi four-component reaction (Ugi-4CR) and copper-catalyzed intramolecular amide-aryl cyclization of heteroaryl chloride with amide has been developed for the synthesis of functionalized 1H-pyrrolo[2,3-b]quinolines in moderate to good yields. The synthesized pyrrolo-fused quinoline was further examined for Pd-catalyzed intramolecular cyclization to afford [1,4]oxazine-fused pyrrolo quinoline 11 and to nucleophilic substitution reactions with allyl bromide and methyl iodide to afford the corresponding allyl and methyl ethers, 12 and 13, respectively." @default.
- W2951839861 created "2019-06-27" @default.
- W2951839861 creator A5004575489 @default.
- W2951839861 creator A5043974342 @default.
- W2951839861 creator A5069911175 @default.
- W2951839861 creator A5082172035 @default.
- W2951839861 date "2015-02-01" @default.
- W2951839861 modified "2023-09-23" @default.
- W2951839861 title "Facile synthesis of functionalized 1H-pyrrolo[2,3-b]quinolines via Ugi four-component reaction followed by Cu-catalyzed aryl-amide, C–N bond coupling" @default.
- W2951839861 cites W1540822500 @default.
- W2951839861 cites W1971723378 @default.
- W2951839861 cites W1973491523 @default.
- W2951839861 cites W1979003465 @default.
- W2951839861 cites W1980331859 @default.
- W2951839861 cites W1981717960 @default.
- W2951839861 cites W1982322001 @default.
- W2951839861 cites W1984797717 @default.
- W2951839861 cites W1984942066 @default.
- W2951839861 cites W1986649083 @default.
- W2951839861 cites W1990332746 @default.
- W2951839861 cites W1992300305 @default.
- W2951839861 cites W1998354440 @default.
- W2951839861 cites W2001430735 @default.
- W2951839861 cites W2004942380 @default.
- W2951839861 cites W2006990665 @default.
- W2951839861 cites W2007826979 @default.
- W2951839861 cites W2014795585 @default.
- W2951839861 cites W2022827384 @default.
- W2951839861 cites W2023762862 @default.
- W2951839861 cites W2036357104 @default.
- W2951839861 cites W2036894630 @default.
- W2951839861 cites W2042114937 @default.
- W2951839861 cites W2046349840 @default.
- W2951839861 cites W2048630824 @default.
- W2951839861 cites W2049899111 @default.
- W2951839861 cites W2057351000 @default.
- W2951839861 cites W2059825137 @default.
- W2951839861 cites W2060152337 @default.
- W2951839861 cites W2065651526 @default.
- W2951839861 cites W2066405748 @default.
- W2951839861 cites W2069279756 @default.
- W2951839861 cites W2071851966 @default.
- W2951839861 cites W2076845909 @default.
- W2951839861 cites W2077570682 @default.
- W2951839861 cites W2082267798 @default.
- W2951839861 cites W2087288610 @default.
- W2951839861 cites W2088575882 @default.
- W2951839861 cites W2090350064 @default.
- W2951839861 cites W2092004167 @default.
- W2951839861 cites W2095227400 @default.
- W2951839861 cites W2100121780 @default.
- W2951839861 cites W2110339385 @default.
- W2951839861 cites W2111677437 @default.
- W2951839861 cites W2112613647 @default.
- W2951839861 cites W2116646685 @default.
- W2951839861 cites W2119853999 @default.
- W2951839861 cites W2125465205 @default.
- W2951839861 cites W2127378043 @default.
- W2951839861 cites W2128765492 @default.
- W2951839861 cites W2136711390 @default.
- W2951839861 cites W2140150936 @default.
- W2951839861 cites W2141142101 @default.
- W2951839861 cites W2148612285 @default.
- W2951839861 cites W2157662074 @default.
- W2951839861 cites W2162083881 @default.
- W2951839861 cites W2165518953 @default.
- W2951839861 cites W2175770910 @default.
- W2951839861 cites W2176633748 @default.
- W2951839861 cites W2181174680 @default.
- W2951839861 cites W2317055048 @default.
- W2951839861 cites W2318830103 @default.
- W2951839861 cites W2327267452 @default.
- W2951839861 cites W2949578665 @default.
- W2951839861 cites W2949600281 @default.
- W2951839861 cites W2950156446 @default.
- W2951839861 cites W2950348680 @default.
- W2951839861 cites W2950377037 @default.
- W2951839861 cites W2950444826 @default.
- W2951839861 cites W2950567721 @default.
- W2951839861 cites W2950604539 @default.
- W2951839861 cites W2951330489 @default.
- W2951839861 cites W2951453309 @default.
- W2951839861 cites W2951609209 @default.
- W2951839861 cites W2951711327 @default.
- W2951839861 cites W2951777963 @default.
- W2951839861 cites W2951960722 @default.
- W2951839861 cites W2952044581 @default.
- W2951839861 cites W2952226244 @default.
- W2951839861 cites W2952389867 @default.
- W2951839861 cites W2952536076 @default.
- W2951839861 cites W2952880377 @default.
- W2951839861 cites W2953029538 @default.
- W2951839861 cites W2953101020 @default.
- W2951839861 cites W2953175202 @default.
- W2951839861 cites W4229790567 @default.
- W2951839861 cites W4230922337 @default.
- W2951839861 cites W4245398161 @default.
- W2951839861 doi "https://doi.org/10.1016/j.tetlet.2014.12.140" @default.