Synthesis, Inhaltsverzeichnis Synthesis 2020; 52(06): 882-892DOI: 10.1055/s-0039-1691487 paper © Georg Thieme Verlag Stuttgart · New York Suzuki–Miyaura Cross-Couplings under Acidic Conditions Lucas Pruschinski , Ana-Luiza Lücke , Tyll Freese , Sean-Ray Kahnert , Sebastian Mummel , Andreas Schmidt ∗ Clausthal University of Technology, Institute of Organic Chemistry, Leibnizstrasse 6, 38678 Clausthal-Zellerfeld, Germany eMail: schmidt@ioc.tu-clausthal.de › Institutsangaben Artikel empfehlen Abstract Artikel einzeln kaufen Alle Artikel dieser Rubrik Abstract Suzuki–Miyaura reactions with Pd(PPh3)4 have been carried out using lithium N-phenylsydnone-4-carboxylate as additive, which gave best yields at pH 5.7 in a mixture of acetic acid, water, and sodium carbonate. Reaction parameters such as the Pd source, the solvent, reaction time and temperature, acid, base and carboxylate have been varied and some representative examples of the Suzuki–Miyaura reaction have been examined. Key words Key wordssydnones - sydnone-4-carboxylates - cross-coupling - cooperative catalysis Volltext Referenzen References Recent examples, reviews and applications: 1a Liu R, Zhu G, Ji Y, Zhang G. Eur. J. Org. Chem. 2019; 3217 1b Jo Y.-I, Burke MD, Cheon C.-H. Org. Lett. 2019; 21: 4201 1c Quibell JM, Duan G, Perry GJ. P, Larrosa I. Chem. Commun. 2019; 55: 6445 1d Asako S, Nakajima H, Takai K. Nat. Catal. 2019; 2: 297 1e Gonzalez-Sebastian L, Morales-Morales D. J. Organomet. Chem. 2019; 893: 39 1f Kim S, Kim B, Dogan NA, Yavuz CT. ACS Sustainable Chem. Eng. 2019; 7: 10865 1g Yang X, Kalita SJ, Maheshuni S, Huang Y.-Y. Coord. Chem. Rev. 2019; 392: 35 1h Wu L, Li F, Rao Y, Wen B, Xu L, Zhou M, Tanaka T, Osuka A, Song J. Angew. Chem. Int. Ed. 2019; 58: 8124 1i West MJ, Watson AJ. B. Org. Biomol. Chem. 2019; 17: 5055 2a Bhatthula BK. G, Kanchani JR, Arava VR, Subha MC. S. Tetrahedron 2019; 75: 874 2b Qu J, Helmchen G. Acc. Chem. 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