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  Facile access to chiral non-natural amino acids

Planas, O., & Cornella, J. (2019). Facile access to chiral non-natural amino acids. Nature Catalysis, 2(10), 839-840. doi:10.1038/s41929-019-0367-7.

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Item Permalink: http://hdl.handle.net/21.11116/0000-0004-F0D3-E Version Permalink: http://hdl.handle.net/21.11116/0000-0004-F0D4-D
Genre: Journal Article

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 Creators:
Planas, Oriol1, Author              
Cornella, Josep1, Author              
Affiliations:
1Research Group Cornellà, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_2466693              

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 Abstract: Given the importance of enantioenriched β2- and β3-amino acids as building blocks, direct and versatile methods for their synthesis are highly coveted by organic chemists. Now, using easily accessible 1,3-oxazinane motifs, a regiodivergent and enantioselective C–H functionalization method permits their synthesis in a straightforward and practical fashion.

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Language(s): eng - English
 Dates: 2019-10-11
 Publication Status: Published online
 Pages: 2
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1038/s41929-019-0367-7
 Degree: -

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Title: Nature Catalysis
  Abbreviation : Nat. Catal.
Source Genre: Journal
 Creator(s):
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Publ. Info: Nature Publishing Group
Pages: - Volume / Issue: 2 (10) Sequence Number: - Start / End Page: 839 - 840 Identifier: ISSN: 25201158
CoNE: https://pure.mpg.de/cone/journals/resource/25201158