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. 2019 Jul 25;141(32):12507–12512. doi: 10.1021/jacs.9b06277

Figure 2.

Figure 2

Examples of autotandem phosphacatalytic annulation of amines and carboxylic acids. All yields isolated on 0.4 mmol scale unless indicated otherwise. See Supporting Information for full synthetic details. aIsolated yield on 5.0 mmol scale, with 8 mol % of 4·[O]. bReaction conducted with Ph2SiH2 (4.4 equiv) in MeCN. cReaction conducted at 60 °C for 20 h. dReaction conducted on 0.2 mmol scale using 15 mol % of [4·Br]Br in MeCN at 50 °C for 20–40 h. eYield determined by 1H NMR with internal standard. fReaction conducted with DEMBM. DCE = 1,2-dichloroethane; Bn = benzyl; Ts = tosyl; iBu = isobutyl.