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DOI: 10.1055/s-0039-1691496
Organosilicon-Mediated Organic Synthesis (SiMOS): A Personal Account
We thank National Natural Science Foundation of China (Grant No. 21703051, 21773051, 21801056) and Natural Science Foundation of Zhejiang Province (Grant No. LZ18B020001, LY17B030005, LY17E030003, and LQ19B040001) for financial support of this work.Publikationsverlauf
Received: 04. Oktober 2019
Accepted after revision: 20. Oktober 2019
Publikationsdatum:
11. November 2019 (online)
Abstract
The organosilicon-mediated organic synthesis (SiMOS) has attracted much attention over the recent decades. However, the use of organosilicon reagents with novel catalytic strategies remains to be explored. This Account summarizes our group’s progress mainly based on the application of a wide variety of organosilicon reagents, including allylic silanes, trifluoromethyl silane, acylsilanes, chlorosilanes, hydrosilanes, trimethylsilyldiazomethane, trimethylsiloxyfuran, silanols, α-trimethylsilylmethylacetate, and trimethylsilylcyanide, in catalysis and organic reactions. These transformations were proved to be alternative procedures for the construction of structurally diverse compounds.
1 Introduction
2 The Exploration of New Reactivity of Organosilicon Reagent in Organic Synthesis
2.1 Allylic Silanes
2.2 Trifluomethylsilane (TMSCF3)
2.3 Acylsilanes
2.4 Chlorosilanes and Hydrosilanes
2.5 Trimethylsilyldiazomethane (TMSD)
2.6 Trimethylsiloxyfuran
2.7 Silanols
2.8 Trimethylsilylcyanide (TMSCN)
3 Conclusion and Perspective
-
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For recent reviews, see:
For recent reviews, see:
Representative reviews:
Selected examples:
Oxidation:
Cross-coupling:
Cycloaddition:
Reviews:
For our work on copper-catalyzed conjugate addition of diethylzinc to α,β-unsaturated acylsilanes, see:
For recent reviews, see:
For recent examples, see:
For recent reviews, see:
For selected and recent examples, see: