書誌事項
- タイトル別名
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- The Development of Highly Selective Addition Reactions of Tetraphenyldiphosphine to Carbon-Carbon Unsaturated Bonds
- ジホスフィンを用いた炭素-炭素不飽和結合への高選択的なリン官能基導入法の開発
- ジホスフィン オ モチイタ タンソ タンソ フホウワ ケツゴウ エ ノ コウセンタクテキ ナ リン カンノウキ ドウニュウホウ ノ カイハツ
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Addition reaction of heteroatom compounds to carbon-carbon unsaturated bonds based on the cleavage of heteroatom-heteroatom single bonds is one of the most useful and basic methods for selective introduction of heteroatom functional groups into organic molecules. Recently, we have developed addition reactions of tetraphenyldiphosphine bearing P-P single bond to alkynes in the presence of transition metal catalysts or upon photoirradiation. While the photoinduced radical reactions afford the bisphosphination products, the transition-metal-catalyzed reactions give rise to the hydrophosphination products, surprisingly. Based on the combination of tetraphenyldiphosphine and organic dichalcogenides under photoirradiation conditions, we have revealed regioselective addition of both phosphino and chalcogeno groups to carbon-carbon unsaturated bonds.
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), 705-717, 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
- 1390282680288168832
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- NII論文ID
- 10026869793
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- NII書誌ID
- AN0024521X
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- COI
- 1:CAS:528:DC%2BC3cXovFKjurg%3D
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- ISSN
- 18836526
- 00379980
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- NDL書誌ID
- 10769658
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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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- CiNii Articles
- KAKEN
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- 抄録ライセンスフラグ
- 使用不可