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  Highly enantioselective synthesis of 1,2-amino alcohol derivatives via proline-catalyzed Mannich reaction

Pojarliev, P., Biller, W., Martin, H., & List, B. (2003). Highly enantioselective synthesis of 1,2-amino alcohol derivatives via proline-catalyzed Mannich reaction. Synlett, 12, 1903-1905. doi:10.1055/s-2003-41491.

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 Creators:
Pojarliev, P.1, Author
Biller, WT1, Author
Martin, Heinz2, Author           
List, Benjamin3, Author           
Affiliations:
1Scripps Res Inst, Dept Mol Biol, 10550 N Torrey Pines Rd, La Jolla, CA 92037 USA, ou_persistent22              
2Research Group Martin, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445613              
3Research Department List, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445585              

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Free keywords: multicomponent reactions; organocatalysis; oxazolidinones; aminoalcohols
 Abstract: Here we report a new catalytic asymmetric synthesis of oxazolidin-2-ones 4 and Cbz-protected 1,2-amino alcohols 5. Our sequence is based on the chemistry of previously unknown 5-acyloxy-oxazolidin-2-ones, which are obtained via proline-catalyzed direct asymmetric three-component Mannich reaction and Baeyer-Villiger oxidation

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 Dates: 2003-09-29
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1055/s-2003-41491
 Degree: -

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Title: Synlett
  Other : Synlett
Source Genre: Journal
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Publ. Info: -
Pages: - Volume / Issue: 12 Sequence Number: - Start / End Page: 1903 - 1905 Identifier: ISSN: 0936-5214
CoNE: https://pure.mpg.de/cone/journals/resource/954925570856