New Development in Catalytic Asymmetric Alkynylation of Carbonyl Compounds
Bibliographic Information
- Other Title
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- カルボニル化合物の触媒的不斉アルキニル化反応の新展開
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Abstract
The enantionselective addition of terminal acetylenes to aldehydes or ketones affords a direct access to optically active propargyl alcohols which are useful, versatile synthetic intermediates. This mini review focuses on the recent advances in zinc (II) and indium (III) salts-mediated asymmetric alkynylation on carbonyl compounds via in situ "catalytic" generation of metal acetylide.
Journal
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- Journal of Synthetic Organic Chemistry, Japan
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Journal of Synthetic Organic Chemistry, Japan 66 (2), 172-173, 2008
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
- 1390001205312844032
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- NII Article ID
- 10021173826
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- NII Book ID
- AN0024521X
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- ISSN
- 18836526
- 00379980
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- Text Lang
- ja
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- Data Source
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- JaLC
- Crossref
- CiNii Articles
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- Abstract License Flag
- Disallowed