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Olefin Metathesis by First-Row Transition Metals

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CHEMPLUSCHEM
卷 86, 期 6, 页码 924-937

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cplu.202100192

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alkylidenes; first-row transition metals; homogeneous catalysis; metallacycles; metathesis

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Catalytic olefin metathesis using first-row transition metals, such as scandium to nickel, offers the potential for producing fine and commodity chemicals in a cost-effective and environmentally friendly manner. The unique electronic structure of these base metals allows for unusual reactivity, although the active species involved in olefin metathesis are still not fully understood.
Catalytic olefin metathesis based on the second- and third-row transition metals has become one of the most powerful transformations in modern organic chemistry. The shift to first-row metals to produce fine and commodity chemicals would be an important achievement to complement existing methods with inexpensive and greener alternatives. In addition, those systems can offer unusual reactivity based on the unique electronic structure of the base metals. In this Minireview, we summarize the progress of the development of alkylidenes and metallacycles of first-row transition metals from scandium to nickel capable of performing cycloaddition and cycloreversion steps, crucial reactions in olefin metathesis. In addition, we will discuss systems capable of performing olefin metathesis; however, the nature of active species is not yet known.

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