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Development of Pd-Catalyzed Denitrative Couplings
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- Asahara Kitty K.
- Department of Applied Chemistry, Waseda University
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- Kashihara Myuto
- Department of Material Chemsitry, Graduate School of Engineering, Kyoto Univeristy
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- Muto Kei
- Institute for Advanced Study, Waseda University
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- Nakao Yoshiaki
- Department of Material Chemsitry, Graduate School of Engineering, Kyoto Univeristy
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- Yamaguchi Junichiro
- Department of Applied Chemistry, Waseda University
Bibliographic Information
- Other Title
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- パラジウム触媒を用いた脱ニトロ型カップリング反応の開発
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Description
<p>Transition metal-catalyzed cross-coupling between aryl halides and nucleophiles is one of the most reliable C-C and C-heteroatom bond forming reactions. However, preparation of haloarenes usually requires multi-step operation, making the whole cross-coupling process inefficient. Nitroarenes, synthesized by a single-step nitration of arenes, can be attractive alternatives as electrophiles in cross-coupling methodology, but inherent inertness of C(sp2)-NO2 bonds toward metal catalysts has been a bottleneck of general denitrative transformations. Recently, we have overcome this obstacle and achieved direct activation of Ar-NO2 bonds by using Pd/BrettPhos catalysis. Herein, we describe the development of denitrative couplings by Pd/BrettPhos catalyst and its unique suitability from a mechanistic point of view. Deep understanding of reaction mechanism also enabled us to design more active Pd/NHC system.</p>
Journal
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- Journal of Synthetic Organic Chemistry, Japan
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Journal of Synthetic Organic Chemistry, Japan 79 (1), 11-21, 2021-01-01
The Society of Synthetic Organic Chemistry, Japan
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Details 詳細情報について
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- CRID
- 1391131406304615040
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- NII Article ID
- 130007966738
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- ISSN
- 18836526
- 00379980
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- Text Lang
- ja
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- Article Type
- journal article
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- Data Source
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- JaLC
- Crossref
- CiNii Articles
- KAKEN
- OpenAIRE
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- Abstract License Flag
- Disallowed