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Silicon-based cross-coupling reaction: an environmentally benign version

Nakao, Yoshiaki, Hiyama, Tamejiro·2011·Chemical Society Reviews

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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Metadata

Authors
Nakao, Y., & Hiyama, T.
Venue
Chemical Society Reviews
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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CoChat. (2026). Citation check: Silicon-based cross-coupling reaction: an environmentally benign version. https://app.cochat.ai/papers/10.1039/c1cs15122c
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Nakao, Y., & Hiyama, T. (2011). Silicon-based cross-coupling reaction: an environmentally benign version. Chemical Society Reviews. https://doi.org/10.1039/c1cs15122c

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Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.