Matches in SemOpenAlex for { <https://semopenalex.org/work/W3205972567> ?p ?o ?g. }
Showing items 1 to 58 of
58
with 100 items per page.
- W3205972567 abstract ": Triazoles are five-membered aromatic heterocyclics, which could exist in two isosteric forms (1,2,3-triazoles and 1,2,4-triazoles) presenting huge applications in medicinal, agricultural, supramolecular and materials sciences. The drugs fluconazole, ribavirin, cefatrizine and tazobactam, and the herbicides cafenstrole and metosulam are famous examples of triazoles. The aim of this review is to present the main recent examples of Microwave-Assisted Organic Synthesis (MAOS) applied for the synthesis end functionalization of 1,4- and 1,5-disubstituted-1,2,3-triazoles, 1,2,4-triazoles, 3-amino-1,2,4-triazoles, 1,2,4-triazol-3-one and 1,2,4-triazol-3-thiol derivatives. Worth of noting, despite some previous reviews about triazole synthesis, none of them focused exclusively on the importance of MAOS technic in the obtention and derivatization of these compounds." @default.
- W3205972567 created "2021-10-25" @default.
- W3205972567 creator A5020050844 @default.
- W3205972567 creator A5030249797 @default.
- W3205972567 creator A5049021281 @default.
- W3205972567 creator A5068608840 @default.
- W3205972567 creator A5072721136 @default.
- W3205972567 creator A5074390529 @default.
- W3205972567 date "2021-10-11" @default.
- W3205972567 modified "2023-10-04" @default.
- W3205972567 title "Recent Advances in Microwave-Assisted Synthesis and Functionalization of 1,2,3- and 1,2,4-triazoles" @default.
- W3205972567 doi "https://doi.org/10.2174/1385272825666211011111408" @default.
- W3205972567 hasPublicationYear "2021" @default.
- W3205972567 type Work @default.
- W3205972567 sameAs 3205972567 @default.
- W3205972567 citedByCount "1" @default.
- W3205972567 countsByYear W32059725672023 @default.
- W3205972567 crossrefType "journal-article" @default.
- W3205972567 hasAuthorship W3205972567A5020050844 @default.
- W3205972567 hasAuthorship W3205972567A5030249797 @default.
- W3205972567 hasAuthorship W3205972567A5049021281 @default.
- W3205972567 hasAuthorship W3205972567A5068608840 @default.
- W3205972567 hasAuthorship W3205972567A5072721136 @default.
- W3205972567 hasAuthorship W3205972567A5074390529 @default.
- W3205972567 hasConcept C115537861 @default.
- W3205972567 hasConcept C147789679 @default.
- W3205972567 hasConcept C178790620 @default.
- W3205972567 hasConcept C179998833 @default.
- W3205972567 hasConcept C185592680 @default.
- W3205972567 hasConcept C21951064 @default.
- W3205972567 hasConcept C2776923573 @default.
- W3205972567 hasConcept C69610077 @default.
- W3205972567 hasConceptScore W3205972567C115537861 @default.
- W3205972567 hasConceptScore W3205972567C147789679 @default.
- W3205972567 hasConceptScore W3205972567C178790620 @default.
- W3205972567 hasConceptScore W3205972567C179998833 @default.
- W3205972567 hasConceptScore W3205972567C185592680 @default.
- W3205972567 hasConceptScore W3205972567C21951064 @default.
- W3205972567 hasConceptScore W3205972567C2776923573 @default.
- W3205972567 hasConceptScore W3205972567C69610077 @default.
- W3205972567 hasLocation W32059725671 @default.
- W3205972567 hasOpenAccess W3205972567 @default.
- W3205972567 hasPrimaryLocation W32059725671 @default.
- W3205972567 hasRelatedWork W1993488012 @default.
- W3205972567 hasRelatedWork W2018218898 @default.
- W3205972567 hasRelatedWork W2023614083 @default.
- W3205972567 hasRelatedWork W2040286050 @default.
- W3205972567 hasRelatedWork W2417326903 @default.
- W3205972567 hasRelatedWork W3005458421 @default.
- W3205972567 hasRelatedWork W3111552877 @default.
- W3205972567 hasRelatedWork W3202799813 @default.
- W3205972567 hasRelatedWork W4303954693 @default.
- W3205972567 hasRelatedWork W4321376810 @default.
- W3205972567 hasVolume "25" @default.
- W3205972567 isParatext "false" @default.
- W3205972567 isRetracted "false" @default.
- W3205972567 magId "3205972567" @default.
- W3205972567 workType "article" @default.