asymmetric organocatalytic reactions of α,β-unsaturated cyclic ketones

Clicks: 202
ID: 240849
2011
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Abstract
The 1,4-conjugate addition of nucleophiles to α,β-unsaturated carbonyl compounds represents one fundamental bond-forming reaction in organic synthesis. The development of effective organocatalysts for the enantioselective conjugate addition of malonate, nitroalkane and other carbon and heteroatom nucleophiles to cycloenones constitutes an important research field and has been explored in recent years. At the same time, asymmetric Diels-Alder reactions have been developed and often a mechanism has been demonstrated to be a double addition rather than synchronous. This review aims to cover literature up to the end of 2010, describing all the different organocatalytic asymmetric 1,4-conjugate additions even if they are listed as transfer hydrogenation, cycloadditions or desymmetrization of aromatic compounds.
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bartoli2011symmetryasymmetric Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors ;Giuseppe Bartoli;Renato Dalpozzo;Giorgio Bencivenni
Journal journal of hospitality and tourism management
Year 2011
DOI
10.3390/sym3010084
URL
http://www.mdpi.com/2073-8994/3/1/84/
Keywords
organocatalysis michael additionmathematics

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