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Silicon-based cross-coupling reaction: an environmentally benign version
Abstract
Much attention has been paid to the cross-coupling reaction of organosilicon compounds due to their stability, non-toxicity, and natural abundance of silicon. In addition, the silicon-based cross-coupling has many advantages over other cross-coupling protocols. Successful examples of the silicon-based cross-coupling reaction are reviewed, focusing especially on the advances made in the last decade. Having had a number of highly effective palladium catalysts developed mainly for other cross-coupling reactions, the development of the silicon-based protocol owes heavily to the design of organosilicon reagents which effectively undergo transmetalation, a key elemental step of the silicon-based cross-coupling reaction. This tutorial review thus classifies various organosilicon reagents depending on substituents on silicon and surveys their cross-coupling reactions with various electrophiles.
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Cited by
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He, J., Wasa, M., Chan, K. S. L., Shao, Q., & Yu, J.-Q. (2017) · Chemical Reviews · doi:10.1021/acs.chemrev.6b00622 · Cited by 2,036
Synthesis of Heterocycles via Palladium-Catalyzed Carbonylations
Wu, X.-F., Neumann, H., & Beller, M. (2013) · Chemical Reviews · doi:10.1021/cr300100s · Cited by 1,283
Palladium-Catalyzed Cross-Coupling Reactions: A Powerful Tool for the Synthesis of Agrochemicals
Devendar, P., Qu, R.-Y., Kang, W.-M., He, B., & Yang, G.-F. (2018) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.8b03792 · Cited by 448
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Metadata
- Authors
- Nakao, Y., & Hiyama, T.
- Venue
- Chemical Society Reviews
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2011
- Volume
- 40
- Issue
- 10
- Pages
- 4893
- ISSN
- 0306-0012 (ISSN-L)
- 1460-4744
- OpenAlex
- W2137820615
- Cited by
- 762
- References
- 0
- FWCI
- 0.80
- Type
- journal article
- Language
- en
- Open access
- closed
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