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- 檜山 爲次郎
- 京都大学大学院工学研究科材料化学専攻
書誌事項
- タイトル別名
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- Transition Metal-catalyzed Reactions of Organosilicon Reagents Through Intramolecular Activation
- ブンシ ナイ カッセイカ オ リヨウ スル ユウキ ケイソ カゴウブツ ノ センイ キンゾク ショクバイ ハンノウ
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抄録
Tetraorganosilane-type reagents that contain a 2-(hydroxymethyl)phenyl group are invented for silicon-based cross-coupling and carbonyl addition reactions. According to the reagent design, a proximal hydroxy group allows transmetallation of organic groups on silicon with palladium(II), copper(I or II), or rhodium(I) to participate in various transition metal-catalyzed C-C bond forming reactions under mild conditions with excellent chemoselectivity. High stability of the newly developed tetraorganosilicon reagents is demonstrated by their functionalization under various acidic, basic, and oxidative conditions with the silyl group intact. Moreover, simple control of their reactivity by orthogonal protection/deprotection allows highly efficient synthesis of functional molecules such as oligoarenes through iterative cross-coupling/deprotection sequences.
収録刊行物
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- 有機合成化学協会誌
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有機合成化学協会誌 68 (7), 729-737, 2010
公益社団法人 有機合成化学協会
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詳細情報 詳細情報について
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- CRID
- 1390282680288166272
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- NII論文ID
- 10026869893
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- NII書誌ID
- AN0024521X
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- COI
- 1:CAS:528:DC%2BC3cXovFKis7w%3D
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- ISSN
- 18836526
- 00379980
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- NDL書誌ID
- 10769730
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- 本文言語コード
- ja
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- データソース種別
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- JaLC
- NDL
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- 使用不可