recent advances in palladium- catalyzed c h … dung/do.pdf · · 2012-02-09recent advances in...
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Recent Advances in Palladium-Catalyzed C─H Activation/C─C
Cross Coupling
Dung Tien Do March 31, 2011
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Outline
I. Introduction II. Pd-Catalyzed Olefination III. Pd-Catalyzed Arylation IV. Pd-Catalyzed Alkylation & Enantioselective C─H Activation V. Conclusion
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Introduction
Tradditional Pd-Catalyzed C─C Cross Coupling
Pd-Catalyzed C─H Activation/C─C Cross Coupling
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C-H Activation through Cyclopalladation or The Complex-Induced Proximity Effect
Yu, J. Q. et al. Angew. Chem. Int. Ed. 2009,48, 5094-5115 Engle, K. M.; Wang, D. H.; Yu, J. Q. JACS, 2010, 132, 14137-14151
Snieckus, V.; Beak, P. et al. Angew. Chem. Int. Ed. 2004,43, 2206-2225
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Machanistic Manifolds
Lyons, T. W.; Sanford, M. S. Chem. Rev. 2010, 110, 1147-1169
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Pd-Catalyzed Olefination
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Olefination of C(sp2)─H Bonds: PdII/Pd0 Catalysis
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Amide-Directed ortho-Selective Olefination of Arenes
Regioselective Olefination of Pyrroles
Beck, E. M.; Grimster, N. P.; Haltley, R.; Gaunt, M. J. JACS, 2006, 128, 2528
Olefination of C(sp2)─H Bonds: PdII/Pd0 Catalysis
Boele, M. D. K.; van Strijdonck, G. P. F.; de Vries, A. H. M.; Kamer, P. C. J.; de Vries, J. G.; van Leeuwen, P. JACS. 2002, 124, 1586
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meta-Olefination of Electron-Deficient Arenes
Zhang, Y. H.; Shi, B. F.; Yu, J. Q. JACS, 2009, 131, 5027
• The use of a rationally designed mutually repulsive ligand was crucial for C-H activation of electron-deficient arenes
• 1 atm O2 can be used as the sole oxidant • A combination of C-H acidity and steric hindrance seem to govern the reactivity of the
different sites, suggesting a concerted mechanism.
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Carboxylic Acids as The Directing Group
Yu, J. Q. et al. Angew. Chem. Int. Ed. 2009,48, 5094-5115
• Pd(II) is forced to coordinate with the unhindered lone pair of electrons on the oxygen atom B triggering C-H insertion
A working model for cationic counter ions promoted Pd(II)-insertion
• Counter cations coordinate with the carboxylate group in a ҡ2 fashion A
Coordination modes of palladium(II) with carboxylic acids
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Olefination of Phenylacetic Acid Substrates
Wang, D. H.; Engle, K. M,; Shi, B. F.; Yu, J. Q. Science, 2010, 327, 315-319
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Proposed Catalytic Cycle
Engle, K. M.; Wang, D. H.; Yu, J. Q. JACS, 2010, 132, 14137-14151
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Pd(II)-Catalyzed Hydroxyl-Directed C-H Olefination
Lu. Y.; Wang D. H.; Engle, K. M.; Yu, J. Q. JACS, 2010, 132, 5916-5921
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Amide-Directed Olefination of sp3 C-H Bonds
• LiCl addition increase the yield. Solvent choice was critical: polar, strong coordinate amide solvent giving best reactivity
• Order of selectivity: Cyclopropanyl > Methyl > Secondary • More electron-withdrawing CONHAr group improved yield: More electron deficient aryl
gave better yield Wasa, M.; Engle, K. M.; Yu, J. Q. JACS, 2010, 132, 3680-3681
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Pd-Catalyzed Arylation
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Pd-Catalyzed C―H Bonds: Arylation
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C-H Arylation with Prefunctionalized Arylating Reagents (PdII/PdIV)
Sanford’s approach for directed C-H activation/arylation
Kalyani, D.; Deprez, N. R,; Desai, L. V.; Sanford, M. S. JACS, 2005, 127, 7330
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Proposed Mechanism for C-H Arylation of 3-Methyl-2-phenylpyridine (PdII/PdIV)
Deprez, N. R,; Sanford, M. S. JACS, 2009, 127, 11234-11241
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Arylation of C-H Bonds Using ArI
Daugulis, O.; Zaitsev, V. G. Angew. Chem. 2005, 117, 4114 Daugulis, O.; Shabashov, D. J. Org. Chem. 2007, 72, 7720
Daugulis, O.; Shabashov, D.; Do, H.Q. Acc. Chem. Res. 2009, 42, 1074-1086
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Daugulis. O.; Zaitsev, V. G.; Shabashov, D. JACS. 2005, 127, 13154
Pyridine-Directed Arylation of sp3 C―H bonds
• Palladation forming a five-membered ring is prefered. • When the directing group is Pyridyl, primary C―H
bonds react faster than the secondary C―H bonds, allowing for the selective monoarylation of methyl groups.
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Intramolecular Alkane Arylation
• Selective at primary position • Concerted inner-sphere palladation-deprotonation pathway involed a three-center agostic interaction:
Lafrance, M.; Gorelsky, S. I.; Fagnou, K. JACS, 2007, 129, 1470-1471
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Shi’s Amide-Directed Arylation Using Organometallic Reagents
Early study by de Vries and coworkers suggested that reactions of these anilides with Pd(OAc)2 proceed by electrophilic palladation.
These highly reactive anilide substrates can also be ortho coupled with arylboronic acids
Yang, S.; Li, B.; Wan, S.; Shi, Z. JACS , 2007, 129, 6066-6067
Shi, Z. et al. Angew. Chem, 2007, 119, 5650
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Arylation Using Carboxylic Acids as The Directing Group
Wang, D. H.; Mei, T. S.; Yu, J. Q. JACS. 2008, 130, 17676
• Air or Oxygen can be used as oxidants • Wide range of functional groups were tolerated
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Substrate Scope: Phenyl Acetic Acids
Wang, D. H.; Mei, T. S.; Yu, J. Q. JACS 2008, 130, 17676
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Cross Coupling of Unactivated Arenes
Stuart, D. R.; Fagnou, K. Science, 2007, 136, 1172-1175
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Fagnou’s Cross-Coupling of Unactivated Arenes
Stuart, D. R.; Fagnou, K. Science, 2007, 136, 1172-1175
• Microwave heating reduced reaction time to 5 h (typically 48 h) with a slight drop in A:B • A:B can be improved by decreasing catalyst loading • Completely selective for arene cross-coupling, no homo-coupling observed.
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Sanford’s Benzoquinoline/Arene Cross-Coupling
Hull, K. L.; Sanford, M. S. JACS. 2007, 129, 11904-11905
Chemoselectivity for Cross-Couping
Benzoquinoline/Arene Cross-Coupling
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Scope of Benzoquinoline/Arene Cross-Coupling
Hull, K. L.; Sanford, M. S. JACS. 2007, 129, 11904-11905
• Coupling at p- and m- positions was significantly favored over the o-position • Increased methylation of the BQ led to a dramatic decrease in coupling at the o-position
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Preliminary Proposed Mechanism
Hull, K. L.; Sanford, M. S. JACS. 2007, 129, 11904-11905
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Buchwald’s Examples of Using O2 as Sole Oxidant for Cross-Coupling
Brasche, G.; Garcia-Fortanet, J.; Buchwald, S. Org. Lett. 2008, 10, 2207-2010
• Using fewer equiv of arenes • Oxygen (1 atm) is the only oxidant • Regioselectivity is governed by steric factors
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Pd-Catalyzed Alkylation & Enantioselective C─H Activation
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• K2CO3 is critical • The use of bulky solvent was believed to prevent homocoupling and β-hydride
elimination • Oxygen can be used as sole oxidant
Yu, J. Q. et al. JACS, 2008, 130, 7190-7191
Alkylation Using Boronic Acids
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Pd-Catalyzed Enantioselective C-H Activation
Using Pyridine as Directing Group
Shi, B. F.; Maugel, N.; Zhang, Y. H.; Yu, J. Q. Angew. Chem. Int. Ed. 2008,47,4882-4886
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Pd(II)- Catalyzed Enantioselective C-H Olefination of Diphenylacetic Acids
Shi, B. F.; Zhang, Y. H.; Lam, J. K.; Wang. D. H.; Yu, J. Q. JACS, 2010, 132, 460-461
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• Acrylates were found to be efficient coupling partners affording 99% ee
Pd(II)- Catalyzed Enantioselective C-H Olefination of Diphenylacetic Acids
Shi, B. F.; Zhang, Y. H.; Lam, J. K.; Wang. D. H.; Yu, J. Q. JACS, 2010, 132, 460-461
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Conclusion
• However, development in this field is still at an early stage compared to the state of the art of traditional cross-coupling reactions. Major challenges must still be overcome before having broad applicability:
-Air as the oxidant -Reduced catalyst loading -Directing group issues -Regioselectivity -Enantioselectivity
• Various catalytic cycles have been developed to accomplish the olefination, arylation, and alkylation of unactivated C-H bonds. Significant advances in developing novel reactions and mechanistic understanding have broadened applicability of this catalyst.
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Acknowledgements
Advisor: Prof. Jeff Johnson Jeff Johnson Group
Greg Boyce Dan Schmitt Mike Slade Austin Smith Kimberly Steward
Justin Malinowski
Michael Corbett Ryan Carris Scott Krabbe Ericka Malow Rani Ulrich
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Examples of Arylation of C(sp3)-H
Yu, J. Q. et al. JACS, 2007, 129, 3510-3511
• First examples of carboxyl-directed Pd-insertion into sp3 β-C-H bond
• PdII/PdIV pathway is likely
Carboxyl-Directed Arylation
Arylation of C(sp3)-H Using Air as Sole Oxidant
• The presence of K2CO3 is critical. • PdII/Pd0 pathway is likely
Yu, J. Q. et al. JACS, 2008, 130, 7190-7191
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Ligand-Accelerated C-H Activation Reaction
Accelerated Pd(II)-catalyzed C-H Olefination of Phenylacetic Acid Substrates
The Pretransition State Coordination Structures prior to Pd(II)-Mediated C-H Cleavage
Wang, D. H.; Engle, K. M,; Shi, B. F.; Yu, J. Q. Science, 2010, 327, 315-319
• Only BQ gave low conversion after 2 hours (<20%) • Ac-Ile-OH led to higher conversion (>99% in most cases) • Amino acid ligands also enable selectivity for unsymmetric aryl substrates
Engle, K. M.; Wang, D. H.; Yu, J. Q. JACS, 2010, 132, 14137-14151
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Pd-Catalyzed Alkynylation
Tobisu, M.; Ano, Y.; Chatani, N. Org. Lett. 2009, 11, 3250
Amide-directed alkynylation
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Pd-Catalyzed Carboxylation
Amide-directed ortho-carboxylation
Carboxylic acid-directed ortho-carboxylation
Giri, R.; Yu, J. Q. JACS, 2008, 130, 14082-14083 Giri, R.; Lam, J. K.; Yu, J. Q. JACS, 2010, 132, 686-693
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Hydroxyl-Directed C-H Carbonylation
Lu, Y.; Leow, D.; Wang, X.; Engle, K. M.; Yu, J. Q. Chem. Science, 2011, 1-6