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For: Li Z, Zhao F, Ou W, Huang PQ, Wang X. Asymmetric Deoxygenative Alkynylation of Tertiary Amides Enabled by Iridium/Copper Bimetallic Relay Catalysis. Angew Chem Int Ed Engl 2021. [PMID: 34596947 DOI: 10.1002/anie.202111029] [Cited by in Crossref: 12] [Cited by in F6Publishing: 12] [Article Influence: 12.0] [Reference Citation Analysis]
Number Citing Articles
1 Chen H, Wu Z, Shao D, Huang P. Multicatalysis protocol enables direct and versatile enantioselective reductive transformations of secondary amides. Sci Adv 2022;8. [DOI: 10.1126/sciadv.ade3431] [Reference Citation Analysis]
2 Zheng P, Xu W, Wang H, Wang D, Wu X, Xu T. Deoxygenative Arylboration of Aldehydes via Copper and Nickel/Photoredox Catalysis. ACS Catal 2022. [DOI: 10.1021/acscatal.2c05043] [Reference Citation Analysis]
3 Wei L, Wang C. Asymmetric transformations enabled by synergistic dual transition-metal catalysis. Chem Catalysis 2022. [DOI: 10.1016/j.checat.2022.10.031] [Reference Citation Analysis]
4 Zhang Y, Lv C, Hu C, Su Z. Mechanistic Study of Asymmetric Alkynylation of Isatin-Derived Ketimine Mediated by a Copper/Guanidine Catalyst. J Org Chem 2022. [PMID: 36001814 DOI: 10.1021/acs.joc.2c01321] [Reference Citation Analysis]
5 Donnelly LJ, Berthet J, Cantat T. Selective Reduction of Secondary Amides to Imines Catalysed by Schwartz's Reagent**. Angew Chem Int Ed 2022;61. [DOI: 10.1002/anie.202206170] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
6 Wu DP, Ou W, Huang PQ. Ir-Catalyzed Chemoselective Reductive Condensation Reactions of Tertiary Amides with Active Methylene Compounds. Org Lett 2022. [PMID: 35849542 DOI: 10.1021/acs.orglett.2c02045] [Reference Citation Analysis]
7 Zhao F, Jiang F, Wang X. Deoxygenative alkylation of tertiary amides using alkyl iodides under visible light. Sci China Chem . [DOI: 10.1007/s11426-022-1331-y] [Reference Citation Analysis]
8 Donnelly LJ, Berthet J, Cantat T. Selective Reduction of Secondary Amides to Imines Catalysed by Schwartz's Reagent**. Angewandte Chemie. [DOI: 10.1002/ange.202206170] [Reference Citation Analysis]
9 Agrawal T, Perez-Morales KD, Cort JA, Sieber JD. Asymmetric Synthesis of Propargylic α-Stereogenic Tertiary Amines by Reductive Alkynylation of Tertiary Amides Using Ir/Cu Tandem Catalysis. J Org Chem 2022. [PMID: 35435681 DOI: 10.1021/acs.joc.2c00131] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Biallas P, Yamazaki K, Dixon DJ. Difluoroalkylation of Tertiary Amides and Lactams by an Iridium-Catalyzed Reductive Reformatsky Reaction. Org Lett 2022. [PMID: 35258311 DOI: 10.1021/acs.orglett.2c00438] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
11 Okada K, Ueda H, Tokuyama H. Total synthesis of (±)-vinoxine: construction of the bridged pyrido[1,2-a]indole skeleton via Tf2O-mediated Bischler-Napieralski reaction and stereoselective radical cyclization. Org Biomol Chem 2022. [PMID: 35262132 DOI: 10.1039/d2ob00274d] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
12 He Y, Wang Y, Li SJ, Lan Y, Wang X. Deoxygenative Cross-Coupling of Aromatic Amides with Polyfluoroarenes. Angew Chem Int Ed Engl 2022;61:e202115497. [PMID: 35014163 DOI: 10.1002/anie.202115497] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
13 He Y, Wang Y, Li S, Lan Y, Wang X. Deoxygenative Cross‐Coupling of Aromatic Amides with Polyfluoroarenes. Angewandte Chemie. [DOI: 10.1002/ange.202115497] [Reference Citation Analysis]