Abstract:Benzylic halides coupled with 1-alkynyl Grignard reagents in the presence of Co-catalyst.Leave this area blank for abstract info.R' THF room temp.
“…[8] Recently, several benzo-and naphthocarbazole analogs have been explored as potential anticancer agents. Co(acac) 3 , [11] and Cu I [12] are reported. Lewis acid mediated arylation/heteroarylation of benzylic systems is usually explored with the use of arenes and heteroarenes.…”
A ZnBr 2 -mediated arylation of aryl/heteroaryl methyl bromides with arenes at 80°C led to the formation of arylated products, which underwent subsequent 1,5-sigmatropic rearrangement followed by electrocyclization and aromatiza-
“…[8] Recently, several benzo-and naphthocarbazole analogs have been explored as potential anticancer agents. Co(acac) 3 , [11] and Cu I [12] are reported. Lewis acid mediated arylation/heteroarylation of benzylic systems is usually explored with the use of arenes and heteroarenes.…”
A ZnBr 2 -mediated arylation of aryl/heteroaryl methyl bromides with arenes at 80°C led to the formation of arylated products, which underwent subsequent 1,5-sigmatropic rearrangement followed by electrocyclization and aromatiza-
“…[5][6][7] Very recently, several benzo and naphthocarbazole analogs have been explored as potential anticancer agents. 8 Even though, a variety of arylation protocols are known for benzylic bromides, [9][10][11][12] they are yet to be adopted for the arylation of N-protected bromomethylindoles. 13 In continuation of our interest on synthetic elaboration of N-protected bromomethylindoles, 14 we wanted to prepare N-protected-2-benzylindole 2 from the bromo compound 1.…”
“…Benzylic halides have also been shown to couple with the alkynyl Grignard compounds (Table 9.22) [344]. Aside from halides as coupling partners, a unique cross-coupling of alkynylmagnesium reagents and vinylcarbamates to afford the corresponding enynes has been discovered to take place under Ni catalysis [346].…”
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