Matches in SemOpenAlex for { <https://semopenalex.org/work/W3204420557> ?p ?o ?g. }
- W3204420557 endingPage "1098" @default.
- W3204420557 startingPage "1089" @default.
- W3204420557 abstract "Isatin or 1H-indole-2,3-dione or 2,3-dioxindole is an indole derivative. Isatin and its analogs are synthetically useful substances where they may be utilized for the production of a broad range of heterocyclic molecules, which are depicting a wide reach of biological and pharmacological activities, as well as anticancer, anti-inflammatory, antiviral, anticonvulsant, anti-TB, antidiabetic, anti-microbial, antitumor, antimalarial, anti-HIV, antibacterial, anti-analgesic, and antiplasmodial activities. Isatin is a precursor for many synthesized therapeutic molecules that are amenable to pharmacological action and have excellent biological potential. Isatin has a magnificent scaffold for both the natural and synthetic construction of molecules. These molecules are being used in drug therapy such as anticancer, antibiotic, and antidepressant drugs and have many more clinical applications. Due to its privileged scaffolding, the synthetic versatility of isatin has produced many structurally diverse derivatives, including the substitution of mono-, di- and tri- substitution of the aryl rings A and those derived by derivation of isatin nitrogen and C2 and C3 carbon moieties. As a result, improving and expediting access to isatin-related molecules is a challenging study in synthetic organic chemistry." @default.
- W3204420557 created "2021-10-11" @default.
- W3204420557 creator A5040936215 @default.
- W3204420557 creator A5074512521 @default.
- W3204420557 creator A5076217181 @default.
- W3204420557 creator A5089688000 @default.
- W3204420557 creator A5090023495 @default.
- W3204420557 date "2021-11-30" @default.
- W3204420557 modified "2023-09-27" @default.
- W3204420557 title "Synthesis of Isatin and its derivatives containing heterocyclic compounds" @default.
- W3204420557 cites W1692825366 @default.
- W3204420557 cites W1976742261 @default.
- W3204420557 cites W1987251505 @default.
- W3204420557 cites W1991683089 @default.
- W3204420557 cites W1993395257 @default.
- W3204420557 cites W1998347040 @default.
- W3204420557 cites W2006514821 @default.
- W3204420557 cites W2008495872 @default.
- W3204420557 cites W2010344122 @default.
- W3204420557 cites W2013461068 @default.
- W3204420557 cites W2025992592 @default.
- W3204420557 cites W2028931219 @default.
- W3204420557 cites W2030776619 @default.
- W3204420557 cites W2041238765 @default.
- W3204420557 cites W2044254728 @default.
- W3204420557 cites W2046326752 @default.
- W3204420557 cites W2048641541 @default.
- W3204420557 cites W2054251499 @default.
- W3204420557 cites W2057559267 @default.
- W3204420557 cites W2061278360 @default.
- W3204420557 cites W2068355085 @default.
- W3204420557 cites W2070025067 @default.
- W3204420557 cites W2075803207 @default.
- W3204420557 cites W2077403681 @default.
- W3204420557 cites W2080768819 @default.
- W3204420557 cites W2091932917 @default.
- W3204420557 cites W2093310723 @default.
- W3204420557 cites W2095353210 @default.
- W3204420557 cites W2097303062 @default.
- W3204420557 cites W2103215838 @default.
- W3204420557 cites W2112973977 @default.
- W3204420557 cites W2125404728 @default.
- W3204420557 cites W2128788119 @default.
- W3204420557 cites W2142570844 @default.
- W3204420557 cites W2166456106 @default.
- W3204420557 cites W2172993981 @default.
- W3204420557 cites W2175279546 @default.
- W3204420557 cites W2316564895 @default.
- W3204420557 cites W2335461563 @default.
- W3204420557 cites W2538452711 @default.
- W3204420557 cites W2791435623 @default.
- W3204420557 cites W2900816906 @default.
- W3204420557 cites W2908523772 @default.
- W3204420557 cites W2947118849 @default.
- W3204420557 cites W2994442092 @default.
- W3204420557 cites W4312935700 @default.
- W3204420557 cites W90284291 @default.
- W3204420557 cites W2015966720 @default.
- W3204420557 doi "https://doi.org/10.18596/jotcsa.962260" @default.
- W3204420557 hasPublicationYear "2021" @default.
- W3204420557 type Work @default.
- W3204420557 sameAs 3204420557 @default.
- W3204420557 citedByCount "2" @default.
- W3204420557 countsByYear W32044205572023 @default.
- W3204420557 crossrefType "journal-article" @default.
- W3204420557 hasAuthorship W3204420557A5040936215 @default.
- W3204420557 hasAuthorship W3204420557A5074512521 @default.
- W3204420557 hasAuthorship W3204420557A5076217181 @default.
- W3204420557 hasAuthorship W3204420557A5089688000 @default.
- W3204420557 hasAuthorship W3204420557A5090023495 @default.
- W3204420557 hasBestOaLocation W32044205571 @default.
- W3204420557 hasConcept C178790620 @default.
- W3204420557 hasConcept C185592680 @default.
- W3204420557 hasConcept C192527728 @default.
- W3204420557 hasConcept C21951064 @default.
- W3204420557 hasConcept C2777256644 @default.
- W3204420557 hasConcept C32909587 @default.
- W3204420557 hasConcept C71240020 @default.
- W3204420557 hasConceptScore W3204420557C178790620 @default.
- W3204420557 hasConceptScore W3204420557C185592680 @default.
- W3204420557 hasConceptScore W3204420557C192527728 @default.
- W3204420557 hasConceptScore W3204420557C21951064 @default.
- W3204420557 hasConceptScore W3204420557C2777256644 @default.
- W3204420557 hasConceptScore W3204420557C32909587 @default.
- W3204420557 hasConceptScore W3204420557C71240020 @default.
- W3204420557 hasIssue "4" @default.
- W3204420557 hasLocation W32044205571 @default.
- W3204420557 hasLocation W32044205572 @default.
- W3204420557 hasLocation W32044205573 @default.
- W3204420557 hasOpenAccess W3204420557 @default.
- W3204420557 hasPrimaryLocation W32044205571 @default.
- W3204420557 hasRelatedWork W1590054402 @default.
- W3204420557 hasRelatedWork W1969274300 @default.
- W3204420557 hasRelatedWork W1987118295 @default.
- W3204420557 hasRelatedWork W1994655645 @default.
- W3204420557 hasRelatedWork W2091766761 @default.
- W3204420557 hasRelatedWork W2346073318 @default.
- W3204420557 hasRelatedWork W2362839736 @default.