Revision as of 19:29, 26 June 2016 edit Monkbot (talk \| contribs) Bots 3,695,952 edits m →Ruthenium catalysis: Task 11: (brfa trial): cs1\|2 maint: multiple authors/editors fixes; ← Previous edit		Revision as of 15:20, 28 June 2016 edit undo Headbomb (talk \| contribs) Edit filter managers, Autopatrolled, Extended confirmed users, Page movers, File movers, New page reviewers, Pending changes reviewers, Rollbackers, Template editors 473,582 edits m →Silver catalysis: clean up. standardize Chemistry: A European Journal / An Asian Journal using AWB Next edit →
Line 121: Recently, the discovery of a general Ag(I)-catalyzed azide–alkyne cycloaddition reaction (Ag-AAC) leading to 1,4-triazoles is reported. Mechanistic features are similar to the generally accepted mechanism of the copper(I)-catalyzed process. Interestingly, silver(I)-salts alone are not sufficient to promote the cycloaddition. However the ligated Ag(I) source has proven to be exceptional for AgAAC reaction.<ref> {{cite journal \|author1=McNulty, J. \|author2=Keskar, K \|author3=Vemula, R. \| title = The First Well-Defined Silver(I)-Complex-Catalyzed Cycloaddition of Azides onto Terminal Alkynes at Room Temperature \| year = 2011 \| journal = [[Chemistry -: A European Journal]] \| volume = 17 \| issue = 52 \| pages = 14727–14730 \| doi = 10.1002/chem.201103244 \| pmid= 22125272}} </ref> <ref>

Azide-alkyne Huisgen cycloaddition: Difference between revisions