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2. Scope of the Suzuki-Miyaura aminoethylation reaction using organotrifluoroborates. Molander GA; Jean-Gérard L J Org Chem; 2007 Oct; 72(22):8422-6. PubMed ID: 17915931 [TBL] [Abstract][Full Text] [Related]
3. Differentially protected benzenediboronic acids: divalent cross-coupling modules for the efficient synthesis of boron-substituted oligoarenes. Noguchi H; Shioda T; Chou CM; Suginome M Org Lett; 2008 Feb; 10(3):377-80. PubMed ID: 18183990 [TBL] [Abstract][Full Text] [Related]
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5. Suzuki-Miyaura cross-coupling of potassium trifluoro(N-methylheteroaryl)borates with aryl and heteroaryl halides. Molander GA; Ryu D; Hosseini-Sarvari M; Devulapally R; Seapy DG J Org Chem; 2013 Jul; 78(13):6648-56. PubMed ID: 23826939 [TBL] [Abstract][Full Text] [Related]
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8. A Concise and Atom-Economical Suzuki-Miyaura Coupling Reaction Using Unactivated Trialkyl- and Triarylboranes with Aryl Halides. Li H; Zhong YL; Chen CY; Ferraro AE; Wang D Org Lett; 2015 Jul; 17(14):3616-9. PubMed ID: 26125106 [TBL] [Abstract][Full Text] [Related]
9. Miyaura borylation/Suzuki-Miyaura coupling (MBSC) sequence of 4-bromo-2,4'-bithiazoles with halides: straightforward access to a heterocylic cluster of d-series of thiopeptide GE2270. Lassalas P; Berini C; Rouchet JEY; Hédouin J; Marsais F; Schneider C; Baudequin C; Hoarau C Org Biomol Chem; 2018 Jan; 16(4):526-530. PubMed ID: 29292462 [TBL] [Abstract][Full Text] [Related]
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