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  Enamine Catalysis is a Powerful Strategy for the Catalytic Generation and Use of Carbanion Equivalents

List, B. (2004). Enamine Catalysis is a Powerful Strategy for the Catalytic Generation and Use of Carbanion Equivalents. Accounts of Chemical Research, 37(8), 548-557. doi:10.1021/ar0300571.

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Item Permalink: http://hdl.handle.net/11858/00-001M-0000-0014-A4B0-A Version Permalink: http://hdl.handle.net/21.11116/0000-0002-E692-5
Genre: Journal Article

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 Creators:
List, Benjamin1, Author              
Affiliations:
1Research Department List, Max-Planck-Institut für Kohlenforschung, Max Planck Society, Kaiser-Wilhelm-Platz 1, 45470 Mülheim an der Ruhr, ou_1445585              

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 Abstract: The chemistry of preformed enamines, especially their use as enolate equivalents, has been a well-investigated area of research since the early 1950s. However, enamine catalysis, the catalysis of carbonyl transformations via enamine intermediates by using primary and secondary amines as catalysts, has only been fully appreciated as a powerful strategy for asymmetric synthesis since the beginning of this century. Contributions from this laboratory to the revitalized interest in asymmetric enamine catalysis are summarized in this Account.

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Language(s): eng - English
 Dates: 2004-01-052004-05-132004-08-01
 Publication Status: Published in print
 Pages: 10
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1021/ar0300571
 Degree: -

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Title: Accounts of Chemical Research
Source Genre: Journal
 Creator(s):
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Publ. Info: Easton, Pa. : American Chemical Society
Pages: - Volume / Issue: 37 (8) Sequence Number: - Start / End Page: 548 - 557 Identifier: ISSN: 0001-4842
CoNE: https://pure.mpg.de/cone/journals/resource/954925373792