Facile access to chiral non-natural amino acids

Planas, Oriol; Cornella, Josep

doi:10.1038/s41929-019-0367-7

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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: https://hdl.handle.net/21.11116/0000-0004-F0D3-E Version Permalink: https://hdl.handle.net/21.11116/0000-0004-F0D4-D

Genre: Journal Article

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Creators:
Planas, Oriol¹, Author
Cornella, Josep¹, Author

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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: Published Online: 2019-10-11

Publication Status: Published online

Pages: 2

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Rev. Type: Peer

Identifiers: DOI: 10.1038/s41929-019-0367-7

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Title: Nature Catalysis

Abbreviation : Nat. Catal.

Source Genre: Journal

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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