rh(iii)-catalyzed c-h activation and annulation via...
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Rh(III)-catalyzed C-H Activation and
Annulation via Oxidizing Directing Group
Lei Zhang
03/23/2016
Dong Group
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Content
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2
3
4
Oxidizing Directing Groups
Brief Introduction of Internal Oxidants
Alkyne involved Annulation in Hua group
Conclusions
2
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Alkyne involved C–H Activation and Annulation
in Hua group
3
Guo, B.; Hua, R. J. Org. Chem. 2015, 80, 8430.
Zhang, L.; Hua, R. J. Org. Chem. 2014, 79, 11541.
Zheng, L.; Hua, R. J. Org. Chem. 2012, 77, 5794.
Zheng, L.; Hua, R. Chem. Eur. J. 2014, 20, 2352.
Zheng, L.; Hua, R. J. Org. Chem. 2014, 79, 3930.
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Zheng, L.; Ju, J.; Bin, Y.; Hua, R. J. Org. Chem. 2012, 77, 5794.
Zheng, L.; Hua, R. Chem. Eur. J. 2014, 20, 2352.
Rhodium(III)-Catalyzed C–H Activation via an Auto-Formed and
Auto-Cleavable Directing Group
4
Indole, Isoquinoline and Heterocycle-Fused Pyridine Synthesis
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Internal Oxidants
Patureau, F. W.; Glorius, F. Angew. Chem., Int. Ed. 2011, 50, 1977.
Huang, H.; Ji, X.; Wu, W.; Jiang, H. Chem. Soc. Rev. 2015, 44, 1155.
Mo, J.; Wang, L.; Liu, Y.; Cui, X. Synthesis 2015, 47, 439.
The strategy of internal oxidant used in C–H bond activation
Strategies for selective C–H functionalization with DGs
(a)
(b)
(c)
5
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Oxidizing Directing Groups (DGox)
The N–O Bond as Internal Oxidant Directing Group
The N–N Bond as Internal Oxidant Directing Group
The N–S Bond as Internal Oxidant Directing Group
The C–N Bond as Internal Oxidant Directing Group
Huang, H.; Ji, X.; Wu, W.; Jiang, H. Chem. Soc. Rev. 2015, 44, 1155.
Yu, S.; Lan, Y.; Wan, Bo. and Li, X. J. Am. Chem. Soc. 2015, 137, 1623. 6
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N-oxides as DGox
N-acyloxy group as DGox
The N–O Bond as Internal Oxidant Directing Group
Oximes as DGox
N-methoxy/hydroxy group as DGox
7Huang, H.; Ji, X.; Wu, W.; Jiang, H. Chem. Soc. Rev. 2015, 44, 1155.
Mo, J.; Wang, L.; Liu, Y.; Cui, X. Synthesis 2015, 47, 439.
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Alkyne-tethered hydroxamic esters as DGox N-OPiv or N-OBoc group
N-phenoxyacetamide, N-Alkenyloxy amine, O-benzoyl-N,N-diethylhydroxylamine
The N–O Bond as Internal Oxidant Directing Group
8Huang, H.; Ji, X.; Wu, W.; Jiang, H. Chem. Soc. Rev. 2015, 44, 1155.
Mo, J.; Wang, L.; Liu, Y.; Cui, X. Synthesis 2015, 47, 439.
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Oximes and its derivatives
Too, P. C.; Wang Y.-F.; Chiba S. Org. Lett. 2010, 12, 5688.
Zhang, X.; Chen, D.; Zhao, M.; Zhao J.; Jia, A.; Li, X. Adv. Synth. Catal. 2011, 353, 719.
Chiba
Li
9
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Formation of pyridines by the use of
α,β-unsaturated oximines
Too, P. C.; Noji, T.; Lim, Y. J.; Li, X.; Chiba, S. Synlett 2011, 2789.
Hyster, T. K.; Rovis, T. Chem. Commun. 2011, 47, 11846. 10
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Mechanism discuss on C–H activation of
oximines with alkynes
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Neely, J. M.; Rovis, T. J. Am. Chem. Soc. 2013, 135, 66.
Formation of Pyridines by the Cyclization of α,β-Unsaturated
Oximines with Alkenes
12
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Formation of pyridines using acrylic acids
Neely, J. M.; Rovis, T. J. Am. Chem. Soc. 2014, 136, 2735. 13
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One-pot synthesis of isoquinolines
Zheng, L.; Ju, J.; Bin, Y.; Hua, R. J. Org. Chem. 2012, 77, 5794. 14
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Rhodium catalyzed coupling of oximine esters with 1,3-dienes
for the synthesis of isoquinolones
Zhao, D.; Lied, F.; Glorius, F. Chem. Sci. 2014, 5, 2869. 15
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Proposed mechanism
Zhao, D.; Lied, F.; Glorius, F. Chem. Sci. 2014, 5, 2869. 16
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N-hydroxylamine and its derivatives
Guimond, N.; Gouliaras, C.; Fagnou, K. J. Am. Chem. Soc. 2010,132, 6908.
Guimond, N.; Gorelsky, S. I.; Fagnou, K. J. Am. Chem. Soc. 2011, 133, 6449.
Xu, L.; Zhu, Q.; Huang, G.; Cheng, B.; Xia, Y. J. Org. Chem. 2012, 77, 3017. 17
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Guimond, N.; Gorelsky, S. I.; Fagnou, K. J. Am. Chem. Soc. 2011, 133, 6449.
Rhodium(III)-Catalyzed Heterocycle Synthesis Using
Terminal Alkyne and Alkene
18
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Switching reaction pathway through different oxidizing directing groups
Rakshit, S.; Grohmann, C.; Glorius, F. J. Am. Chem. Soc. 2011, 133, 2350.
Rhodium catalyzed C–H functionalization between derevatives of
N-hydroxybenzamide and alkenes
19
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Xu, X.; Liu, Y.; Park, C.-M. Angew. Chem., Int. Ed. 2012, 124, 9506.
Davis, T. A.; Hyster, T. K.; Rovis T. Angew. Chem., Int. Ed. 2013, 52, 14181.
Rhodium(III)-Catalyzed Intramolecular Annulation
20
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Yu, D.-G.; Gensch, T.; Glorius, F. Angew. Chem., Int. Ed. 2014, 53, 9650.
Synthesis of Diverse Bisheterocycles of 1,3-Diyne
21
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Rh(III)-Catalyzed C−H Activation and Annulation with
Alkyne MIDA Boronates
Wang, H.; Glorius, F. J. Am. Chem. Soc. 2012, 134, 19592.
Presset, M.; Molander, G. A. Org. Lett. 2013, 15, 1528. 22
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Huckins, J. R.; Hwang, T.-L.; Bio, M. M. J. Am. Chem. Soc. 2013, 135, 14492.
Rh(III)-Catalyzed C−H Activation for the Regioselective
Synthesis of Naphthyridinones
23
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Fukui, Y.; Tian, P.; Lin, G.-Q. J. Am. Chem. Soc. 2014, 136, 15607.
Rh(III)-Catalyzed Cyclization of Benzamides
and 1,6-Enynes
24
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Wang, H.; Glorius, F. Angew. Chem., Int. Ed. 2012, 51, 7318
Rhodium(III)-Catalyzed C–H Activation and intermolecular
Annulation with Allenes
25
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Formation of Trisubstituted Allenes Using Allenylsilanes
Zeng, R.; Wu, S.; Fu, C. L.; Ma, S. J. Am. Chem. Soc. 2013, 135,18284.
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Hyster, T. K.; Ruhl, K. E.; Rovis, T. J. Am. Chem. Soc. 2013, 135, 5364.
Cui, S.; Zhang, Y; Wang, D.; Wu, Q. Chem. Sci. 2013, 4, 3912.
Rh(III)-Catalyzed Coupling of Benzamides
and Diazo Compounds
27
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Hyster, T. K.; Rovis, T. Synlett 2013, 1842.
Synthesis of Isoquinolones from Amides and Cyclopropenes
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Cui, S.; Zhang, Y.; Wu, Q. Chem. Sci. 2013, 4, 3421.
Rh(III)-catalyzed C–H Activation/Cycloaddition of
Benzamides and Methylenecyclopropanes
29
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Proposed Mechanism
Cui, S.; Zhang, Y.; Wu, Q. Chem. Sci. 2013, 4, 3421. 30
A
B
C
D
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Zhang, Y.; Zheng, J.; Cui, S. J. Org. Chem. 2014, 79, 6490.
Rh(III)-Catalyzed C−H Activation/Cyclization
of Indoles and Pyrroles
31
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Zhang, Y.; Zheng, J.; Cui, S. J. Org. Chem. 2014, 79, 6490.
Proposed Mechanism
32
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Rhodium catalyzed coupling between N-phenoxyamides
and cyclopropenes
Zhang, H.; Wang, J. Angew. Chem., Int. Ed. 2014, 53, 13234. 33
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Rh(III)-Catalyzed Cyclopropanation Initiated by C−H Activation
Piou, T.; Rovis, T. J. Am. Chem. Soc. 2014, 136, 11292. 34
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Rhodium catalyzed cyclization of O-benzoyl-N,N-
diethylhydroxylamine with alkynes
Li, X. G.; Liu, K.; Zou, G.; Liu, P. N. Adv. Synth. Catal. 2014, 356, 1496. 35
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The N–N Bond as Internal Oxidant Directing Group
Liu, B.; Song, C.; Sun, C.; Zhou, S.; Zhu, J. J. Am. Chem. Soc. 2013, 135, 16625.
Wang, C.; Huang, Y. Org. Lett. 2013, 15, 5294. 36
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Synthesis of Indoles Using N—N Bond as the Internal Oxidant
Zhao, D.; Shi, Z.; Glorius, F. Angew. Chem., Int. Ed. 2013, 52, 12426.
Zheng, L.; Hua, R. Chem. Eur. J. 2014, 20, 2352.
Muralirajana, K.; Cheng, C. H. Adv. Synth. Catal. 2014, 356, 1571. 37
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Proposed reaction mechanism for the indole synthesis
from hydrazine
Zhao, D.; Shi, Z.; Glorius, F. Angew. Chem., Int. Ed. 2013, 52, 12426. 38
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Rhodium(III)-catalyzed the formation of isoquinolines
using hydrazine as an oxidizing directing group
Chuang, S.-C.; Gandeepan, P.; Cheng, C.-H. Org. Lett. 2013, 15, 5750. 39
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The N–S Bond as Internal Oxidant Directing Group
Zhang, Q.-R.; Huang, J.-R.; Zhang, W.; Dong, L. Org. Lett. 2014, 16, 1684. 40
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The C–N Bond as Internal Oxidant Directing Group
Rhodium-Catalyzed C−H Activation of Phenacyltriethylammonium
Yu, S.; Liu, S.; Lan, Y.; Wan, B.; Li, X. J. Am. Chem. Soc. 2015, 137, 1623.41
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Conclusions
The ‘internal oxidant’ strategy has emerged as a powerful tool
in metal-catalyzed direct C-H activation reactions;
As direction group: improve the reactivity and selectivity of C-
H functionalization, broaden the substrate scope and decreasing
the amount of waste formation;
Further development focus on finding new types of internal
oxidants and improving the mechanistic understanding.
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THANK YOU FOR YOUR ATTENTION!
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