Efficient Proline-Catalyzed Michael Additions of Unmodified Ketones to Nitro 
Olefins

List, Benjamin; Pojarliev, Peter; Martin, Harry J.

doi:10.1021/ol015799d

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Efficient Proline-Catalyzed Michael Additions of Unmodified Ketones to Nitro Olefins

List, B., Pojarliev, P., & Martin, H. J. (2001). Efficient Proline-Catalyzed Michael Additions of Unmodified Ketones to Nitro Olefins. Organic Letters, 3(16), 2423-2425. doi:10.1021/ol015799d.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0014-A4D9-0 Version Permalink: https://hdl.handle.net/21.11116/0000-0008-38DA-4

Genre: Journal Article

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Creators:
List, Benjamin¹, Author
Pojarliev, Peter¹, Author
Martin, Harry J.¹, 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: Here we describe the proline-catalyzed Michael addition of unmodified ketones to nitro olefins. This novel reaction provides γ-nitro ketones in modest enantioselectivity yet excellent yields.

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Language(s): eng - English

Dates: Submitted: 2001-03-06Published Online: 2001-07-14Date issued: 2001-08-09

Publication Status: Issued

Pages: 3

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Table of Contents: -

Rev. Type: Peer

Identifiers: DOI: 10.1021/ol015799d

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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 (16) Sequence Number: - Start / End Page: 2423 - 2425 Identifier: ISSN: 1523-7060
CoNE: https://pure.mpg.de/cone/journals/resource/954925626338