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- W2950999505 endingPage "9085" @default.
- W2950999505 startingPage "9076" @default.
- W2950999505 abstract "A modular, multicomponent synthesis of 1,2,3,4-tetrasubstituted pyrroles promoted by the inexpensive CeCl3·7H2O, is reported. The reaction was carried out under microwave irradiation, affording good yields of products in short time. Scope and limitations were explored and a plausible reaction mechanism is discussed. The resulting heterocycles were smoothly and efficiently converted into their corresponding 5-arylsulfenyl derivatives by reaction with diaryl disulfides and trichloroisocyanuric acid in EtOAc." @default.
- W2950999505 created "2019-06-27" @default.
- W2950999505 creator A5028967934 @default.
- W2950999505 creator A5047366093 @default.
- W2950999505 creator A5052453155 @default.
- W2950999505 creator A5061009958 @default.
- W2950999505 creator A5064787594 @default.
- W2950999505 date "2013-10-01" @default.
- W2950999505 modified "2023-10-12" @default.
- W2950999505 title "Modular CeCl3·7H2O-catalyzed multi-component synthesis of 1,2,3,4-tetrasubstituted pyrroles under microwave irradiation and their further trichloroisocyanuric acid-mediated conversion into 5-sulfenylpyrrole derivatives" @default.
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