On August 16, 2019, Khan, Faiyaz; Fatima, Mehvish; Shirzaei, Moheb; Vo, Yen; Amarasiri, Madushani; Banwell, Martin G.; Ma, Chenxi; Ward, Jas S.; Gardiner, Michael G. published an article.Application of 65417-22-3 The title of the article was Tandem Ullmann-Goldberg Cross-Coupling/Cyclopalladation-Reductive Elimination Reactions and Related Sequences Leading to Polyfunctionalized Benzofurans, Indoles, and Phthalanes. And the article contained the following:
On exposure to a combination of Cu[I]- and Pd[0]-based catalysts, compounds such as halophenols and halocycloalkenones engage in tandem Ullmann-Goldberg cross-coupling and cyclopalladation-reductive elimination reactions to give benzofurans. Related reactions involving hetero-Michael additions of o-halogenated phenols or anilines to propiolates and the Pd[0]-catalyzed cyclization of the resulting conjugates provide, in a one-pot process, alternately functionalized benzofurans, indoles, or phthalanes. The experimental process involved the reaction of Methyl 2-methyl-1H-indole-3-carboxylate(cas: 65417-22-3).Application of 65417-22-3
The Article related to halophenol haloenone ullmann goldberg cross coupling cyclopalladation reductive elimination, benzofuran preparation, indole preparation, phthalane preparation, Heterocyclic Compounds (One Hetero Atom): Indoles, Indolizines, Carbazoles, and Other Arenopyrroles and other aspects.Application of 65417-22-3
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Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles