Highly Enantioselective Transfer Hydrogenation of α,β-Unsaturated Ketones

Martin, Nolwenn J. A.; List, Benjamin

doi:10.1021/ja065708d

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Highly Enantioselective Transfer Hydrogenation of α,β-Unsaturated Ketones

Martin, N. J. A., & List, B. (2006). Highly Enantioselective Transfer Hydrogenation of α,β-Unsaturated Ketones. Journal of the American Chemical Society, 128(41), 13368-13369. doi:10.1021/ja065708d.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-000F-9369-0 Version Permalink: https://hdl.handle.net/21.11116/0000-0008-40C7-F

Genre: Journal Article

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Creators:
Martin, Nolwenn J. A.¹, Author
List, Benjamin¹, Author

Affiliations:
1Research Department List, Max-Planck-Institut für Kohlenforschung, Max Planck Society, ou_1445585

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Abstract: We describe an efficient and highly enantioselective conjugate transfer hydrogenation of α,β-unsaturated ketones that is catalyzed by a salt made from tert-butyl valinate and a recently introduced powerful chiral phosphoric acid catalyst (TRIP).

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Language(s): eng - English

Dates: Submitted: 2006-08-07Published Online: 2006-09-21Date issued: 2006-10-01

Publication Status: Issued

Pages: 2

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Rev. Type: Peer

Identifiers: DOI: 10.1021/ja065708d

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Title: Journal of the American Chemical Society

Other : JACS

Abbreviation : J. Am. Chem. Soc.

Source Genre: Journal

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Publ. Info: Washington, DC : American Chemical Society

Pages: - Volume / Issue: 128 (41) Sequence Number: - Start / End Page: 13368 - 13369 Identifier: ISSN: 0002-7863
CoNE: https://pure.mpg.de/cone/journals/resource/954925376870