書誌事項
- タイトル別名
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- Selective Synthesis of Organoboron Compounds with Copper(I)-Phosphine Complex Catalysts
- ドウ(I)- ホスフィン サクタイ ショクバイ オ モチイタ ユウキ ホウソ カゴウブツ ノ センタクテキ ゴウセイホウ
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Transition-metal-catalyzed borylation has emerged as a powerful method for preparation of organoboron compounds, which are useful synthetic reagents in organic synthesis. However, chemo-, regio-, and stereoselective synthesis of the boron compounds are still highly required.<br>Herein, we report copper(I)-catalyzed boryl substitution of allylic carbonates and ethers, monoborylation of 1,3-dienes and enynes, boryl substitution of alkyl halides, and borylative cyclization of alkenes containing an appropriate leaving group for the selective synthesis of various organoboron compounds including allyl- and allenylboronates, and optically active carbocyclic boronates. Preparation of the borylation products has been difficult with known procedures. In addition, direct enantio-convergent transformation of racemic substrates without a racemization or symmetrization process, a novel methodology for asymmetric synthesis with racemic substrates, is also reported.
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 72 (7), 758-769, 2014
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
- 1390282680316646784
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- NII論文ID
- 130004679607
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- NII書誌ID
- AN0024521X
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- ISSN
- 18836526
- 00379980
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- NDL書誌ID
- 025635231
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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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- 抄録ライセンスフラグ
- 使用不可