Matches in SemOpenAlex for { <https://semopenalex.org/work/W2044293896> ?p ?o ?g. }
- W2044293896 endingPage "1075" @default.
- W2044293896 startingPage "1069" @default.
- W2044293896 abstract "Abstract The synthesis of indole derivatives by the treatment of aryl hydrazones coupled from aromatic hydrazines and ketones or aldehydes with either a mineral or Lewis acid is generally known as the Fischer indole synthesis. Although the mechanism of this reaction has been extensively studied, the one formulated by Robinson and Robinson is now generally accepted. Thioether is often used to direct the regiochemistry and it has also been reported that Eaton's reagent (P 2 O 5 /MeSO 3 H) and diethylaluminum 2,2,6,6‐tetramethylpiperidide (DATMP) can facilitate the regioselectivity. A solid‐phase supported synthesis of indole has been developed. Several modifications of this reaction have been applied to achieve the optimum yield. This reaction has been widely applied to pharmaceutical and medicinal chemistry as well as in organic synthesis." @default.
- W2044293896 created "2016-06-24" @default.
- W2044293896 creator A5025993879 @default.
- W2044293896 date "2010-09-15" @default.
- W2044293896 modified "2023-10-12" @default.
- W2044293896 title "Fischer Indole Synthesis" @default.
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