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  Proline-Catalyzed Asymmetric Aldol Reactions between Ketones and α-Unsubstituted Aldehydes

List, B., Pojarliev, P., & Castello, C. (2001). Proline-Catalyzed Asymmetric Aldol Reactions between Ketones and α-Unsubstituted Aldehydes. Organic Letters, 3(4), 573-575. doi:10.1021/ol006976y.

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 Creators:
List, Benjamin1, Author           
Pojarliev, Peter1, Author
Castello, Chris1, Author
Affiliations:
1The Skaggs Institute for Chemical Biology and the Department of Molecular Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA., ou_persistent22              

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 Abstract: With this communication we extend the methodology of proline-catalyzed direct asymmetric aldol reactions to include α-unsubstituted aldehydes as acceptors. This important aldehyde class gives the corresponding aldols in 22−77% yield and up to 95% ee when the reactions are performed in pure acetone or in ketone/chloroform mixtures. On the basis of these results we have developed a concise new synthesis of (S)-ipsenol.

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Language(s): eng - English
 Dates: 2000-12-072001-01-252001-02-01
 Publication Status: Issued
 Pages: 3
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1021/ol006976y
 Degree: -

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Title: Organic Letters
  Abbreviation : Org. Lett.
Source Genre: Journal
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Publ. Info: Washington, DC : American Chemical Society
Pages: - Volume / Issue: 3 (4) Sequence Number: - Start / End Page: 573 - 575 Identifier: ISSN: 1523-7060
CoNE: https://pure.mpg.de/cone/journals/resource/954925626338