Aqueous Suzuki‐Miyaura Reaction with 0.6 Equiv. of Base: Green and Efficient Access to Biaryls and Unsymmetrical Terphenyls. Issue 21 (4th June 2018)

• Record Type: Journal Article
• Authors: Li, Xinmin; Teng, Yong; Feng, Fangfang; Hu, Qinghong; Yuan, Zeli
• Is Part Of: ChemistrySelect. Volume 3:Issue 21(2018)
• Page Start: 6022
• Page End: 6027
• Publication Date: 2018-06-04
• Subjects: Ligand-free -- One-pot -- Reducing base -- Suzuki reaction -- Terphenyls; Chemistry -- Periodicals; 540.5
• DOI: 10.1002/slct.201800946
• Languages: English
• ISSNs: 2365-6549

Abstract

Abstract: A ligand‐free palladium‐catalyzed Suzuki–Miyaura reaction in water with 0.6 equiv. of base is described. This method enables the preparation of a variety of biaryls in high yields. Additionally, using bromo‐ N ‐methyliminodiacetic acid (MIDA) boronates as building block, one‐pot double Suzuki–Miyaura reaction has been achieved by controlling the amount of base, and various unsymmetrical terphenyls were prepared in moderate to good yields. Abstract : Using 1 mol% Pd(OAc)2 as catalyst and 0.6 equiv. of K2 CO3 as base, various of aryl/hetero bromides coupled with arylboronic acids in water to provide the biaryl products in good yields. Additionally, one‐pot double Suzuki‐Miyaura cross‐coupling reactions was achieved by controlling the amount of base, and a series of unsymmetrical terphenyls were prepared in moderate to good yields.