Syntheses and Reactions of Multifunctional Carbanions "Ynolate Anions".
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- Shindo Mitsuru
- Institute for Medicinal Resources, University of Tokushima
Bibliographic Information
- Other Title
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- 機能性カルバニオン「イノラートアニオン」の合成と反応
- キノウセイ カルバニオン イノラートアニオン ノ ゴウセイ ト ハンノウ
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Abstract
Ynolates are carbanions having a triple bond in place of the double bond in enolate anions. Ynolates are ketene anion equivalents, thus ynolates introduce a ketene unit into substrates and the resulting products possess high reactivity. This allows ynolates to undergo unique reaction sequences. For the past 20 years, several methods for the generation of ynolates and their reactions have been developed. Recently, we have developed a highly efficient method for their generation and new rections such as olefination, tandem [2+2] cycloaddition-Dieckmann condensation, syntheses of β-lactams. In this review, an overview of the syntheses and the reactions of ynolates, especially focusing our recent results, are described.
Journal
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- Journal of Synthetic Organic Chemistry, Japan
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Journal of Synthetic Organic Chemistry, Japan 58 (12), 1155-1166, 2000
The Society of Synthetic Organic Chemistry, Japan
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Keywords
Details 詳細情報について
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- CRID
- 1390001205278637952
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- NII Article ID
- 10008824458
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- NII Book ID
- AN0024521X
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- COI
- 1:CAS:528:DC%2BD3MXhs1GgsQ%3D%3D
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- ISSN
- 18836526
- 00379980
- http://id.crossref.org/issn/00379980
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- NDL BIB ID
- 5593964
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- Text Lang
- ja
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- Data Source
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- JaLC
- NDL
- Crossref
- CiNii Articles
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- Abstract License Flag
- Disallowed