Metal Complexes-catalyzed Hydrolysis, Alcoholysis, and Hydroalkoxylation
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- Tokunaga Makoto
- Department of Chemistry, Kyushu University JST (Japan Science and Technology Agency), CREST
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- Hamasaki Akiyuki
- Department of Chemistry, Kyushu University
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- Yamamoto Eiji
- Department of Chemistry, Kyushu University
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- Itoh Hisashi
- Department of Chemistry, Kyushu University
Bibliographic Information
- Other Title
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- 金属錯体触媒による加水分解,加アルコール分解およびアルコールの付加反応
- キンゾク サクタイ ショクバイ ニ ヨル カスイ ブンカイ カアルコール ブンカイ オヨビ アルコール ノ フカ ハンノウ
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Abstract
In this accounts, we describe our recent studies on hydrolysis, alcoholysis, and addition of alcohols to organic molecules. The reactions utilizing water and alcohols as a reagent are one of the most basic and simple reactions. The palladium-catalyzed asymmetric hydrolysis and alcoholysis of vinyl ethers gave valuable axially-chiral 1,1'-bi-2-naphthol and 1,1'-bi-2-phenol derivatives and chiral P-chirogenic compounds in optically active form. The reaction is applied for hydrolytic deallylation of N-allyl amide and allyl esters. The later one was achieved by palladium/ruthenium dual catalysts which is the first example of catalytic irreversible ester hydrolysis. Gold complexes also catalyzed vinyl ether alcoholysis and hydroalkoxylation of olefins. In the later reaction, simple unactivated olefins can be used as substrates and gave the product in 92% yield. The copper-DTBM-SEGPHOS complex catalyzed alcoholysis of azlactones which is the first example showing zero-order kinetic resolution.
Journal
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- Journal of Synthetic Organic Chemistry, Japan
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Journal of Synthetic Organic Chemistry, Japan 68 (7), 738-744, 2010
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
- 1390001205311457536
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- NII Article ID
- 10026869968
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- NII Book ID
- AN0024521X
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- COI
- 1:CAS:528:DC%2BC3cXovFKis7o%3D
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- ISSN
- 18836526
- 00379980
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- NDL BIB ID
- 10769751
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- Text Lang
- ja
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- Data Source
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- JaLC
- NDL
- Crossref
- CiNii Articles
- KAKEN
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- Abstract License Flag
- Disallowed