N,B-Bidentate Boryl Ligand-Supported Iridium Catalyst for C H Borylation
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1 N,B-Bidentate Boryl Ligand-Supported Iridium Catalyst for C H Borylation Reporter: Bo Song Checker: Yue Ji Date: 2017/01/03 Wang, G.; Liu, L.; Wang, H.; Li, P. J. Am. Chem. Soc. 2017, 139, ASAP. Pengfei Li ( 李鹏飞 ) 西安交通大学
2 Contents Introduction N,B-Bidentate Boryl Ligand-Supported Iridium Catalyst for C H Borylation Summary
3 Introduction
4 Introduction Segawa, Y.; Yamashita, M.; Nozaki, K. J. Am. Chem. Soc. 2009,131, Stern, C. L.; Seideman, T.; Mirkin, C. A. J. Am. Chem. Soc. 2009, 131, 9482.
5 Introduction
6 Introduction Braunschweig, H.; Kupfer, T.; Lutz, M. Angew. Chem. Int. Ed. 2006, 45, 8048.
7 Introduction Schubert, H.; Leis, W.; Wesemann, L. Chem. Commun. 2014, 50, 2738.
8 Boryl Ligands Wang, G.; Xu, L.; Li, P. J. Am. Chem. Soc. 2015, 137, 8058.
9 N,B-Type Bidentate Boryl Ligands
10 Double N,B-Ligands for C-H Borylation Preparation of Preligand PL-1 and Their Iridium Complexes Wang, G.; Xu, L.; Li, P. J. Am. Chem. Soc. 2015, 137, 8058.
11 Double N,B-Ligands for C-H Borylation Comparison of Preligand PL-1 with Tmphen in Borylation Wang, G.; Xu, L.; Li, P. J. Am. Chem. Soc. 2015, 137, 8058.
12 Substrate Scope of C H Borylation with PL-1
13 Substrate Scope of C H Borylation with PL-1 Wang, G.; Xu, L.; Li, P. J. Am. Chem. Soc. 2015, 137, 8058.
14 Ir-Catalyzed Directed ortho C-H Borylation Ros, A.; Fernandez, R.; Lassaletta, J. M. Chem. Soc. Rev. 2014, 43, Kawamorita, S.; Fukuoka, A.; Sawamura, M. J. Am. Chem. Soc. 2009, 131, 5058.
15 Ir-Catalyzed Directed ortho C-H Borylation Krska, S. W.; Maleczka, R. E.; Smith, M. R., III. J. Am. Chem. Soc. 2014, 136, Wang, G.; Liu, L.; Wang, H.; Li, P. J. Am. Chem. Soc. 2017, 139, ASAP.
16 Single N,B-Ligand for Directed ortho Borylation Preparation of Preligand PL-2 and Their Iridium Complexes Wang, G.; Liu, L.; Wang, H.; Li, P. J. Am. Chem. Soc. 2017, 139, ASAP.
17 Single N,B-Ligand for Directed ortho Borylation Catalyst Screening for ortho Borylation entry a precatalyst conv. (%) b yield (%) b ratio of o/(m+p) b 1 2a/[Ir(OMe)(cod)] (5a) 5:95 2 2a/[IrCl(cod)] complex 3a b/[Ir(OMe)(cod)] (5a) + 4 (5a ) 69:31 5 2b/[IrCl(cod)] (5a) + 1 (5a ) 91:9 6 complex 3b (5a) + 3 (5a ) 91:9 7 2c/[IrCl(cod)] (5a) + 13 (5a ) >99:1 8 2c/[Ir(OMe)(cod)] (5a) 35:65 a Reaction conditions: methyl benzoate 4a (0.5 mmol), B 2 pin 2 (0.5 mmol), [Ir(X)(cod)] 2 (0.005 mmol), preligand (0.01 mmol) or complex (0.01 mmol) in 1.0 ml of n-hexane, 80 o C, 8 h. b Conversion, yield, and ratio were based on 1 H NMR analyses of the crude products.
18 Scope of ortho-borylation of Arenoates
19 Scope of Arene with Different Directing Groups
20 Single N,B-Ligand for Directed ortho Borylation C(sp 3 ) H Borylation Using Preligand 2c Wang, G.; Liu, L.; Wang, H.; Li, P. J. Am. Chem. Soc. 2017, 139, ASAP.
21 Summary
22 The Frist Paragraph Boryl ligands, formally with a negatively charged sp 2 hybridized boron as the coordinating atom, are isoelectronic with carbene ligands. In sharp contrast to the broad applications of carbene ligands, boryl ligands have been rarely used as supporting ligands in transition-metal catalysis. The utilization of metal-boryl catalysts have been challenging because (1) methods for introducing boryls onto metals in a convenient and reliable way are limited and (2) the resulting B M bonds are highly reactive, often leading to loss of the boryl groups in subsequent steps.
23 The Last Paragraph In conclusion, we have designed and prepared new pyridine tethered silylboranes and demonstrated their utility as convenient precursors for introducing a single N,B-bidentate ligand onto iridium via B Si oxidative addition. The preligands are structurally modifiable. Based on these preligands, we have developed a highly effective and practical catalyst system for directed C(sp 2 ) H and C(sp 3 ) H borylation of a broad range of substrates.
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