2018
DOI: 10.2174/1385272821666171009155750
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Recent Applications of 2,2-Disubstituted-1,3-Dicarbonyls

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Cited by 6 publications
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“…They were three‐component reactions of ketones, amines, and sulfonyl hydrazides. Especially, 1,3‐dicarbonyls acted as important intermediates in organic synthesis. I 2 functioned as a Lewis acid for the cyclization, as well as the reaction promoter for the formation of RSI (Scheme ).…”
Section: Electrophilic Rx Intermediatesmentioning
confidence: 99%
“…They were three‐component reactions of ketones, amines, and sulfonyl hydrazides. Especially, 1,3‐dicarbonyls acted as important intermediates in organic synthesis. I 2 functioned as a Lewis acid for the cyclization, as well as the reaction promoter for the formation of RSI (Scheme ).…”
Section: Electrophilic Rx Intermediatesmentioning
confidence: 99%
“…The use of 1,3‐dicarbonyls as synthetic building blocks [11b,c] in total synthesis, directing groups for C sp2 −H bond cleavage, [11d] as well as a leaving group, [11e,f] has been reported. Xia's work provided a mild combination of readily available 1,3‐dicarbonyls, alkenes, and quinolines for the construction of more complex carbon frameworks.…”
Section: Radical Reactionsmentioning
confidence: 99%
“…Then, carbazoles were obtained by subsequent cyclization and aromatization. 1,3‐dicarbonyls have been widely used as synthetic building blocks in organic chemistry [14d,e] . Xue and co‐worker [14c] developed the I 2 ‐promoted construction of indolo[2,3‐b]carbazoles.…”
Section: Nucleophilic C3mentioning
confidence: 99%