articleTop 1% cited
Mechanistic Manifold and New Developments of the Julia–Kocienski Reaction
European Journal of Organic Chemistry · 2009 · Vol. 2009(12) · pp. 1831–1844
Christophe Aïssa✉(University of Liverpool)
Abstract
Abstract The Julia–Kocienski reaction has become indispensable in the synthetic organic chemist's olefination toolbox. Although the stereochemical outcome of the transformation is sometimes difficult to predict, some trends can be explained by an array of mechanistic hypotheses which have been put forward since the initial disclosure of the reaction. Moreover, several important developments have been recently reported and are summarised in this microreview. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
Synthetic Organic Chemistry MethodsAsymmetric Synthesis and CatalysisChemical Synthesis and AnalysisChemistryToolboxBiochemical engineeringManifold (fluid mechanics)Computer scienceEngineering
Funding
- Research Councils UK
Citations
256
FWCI
11.17
field-weighted impact
References
111
Percentile
99%
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References
Syntheses a l'aide de sulfones v(+)- methode de synthese generale de doubles liaisons.
Tetrahedron Letters · 1973 · 595 citations
A direct synthesis of olefins by reaction of carbonyl compounds with lithio derivatives of 2-[alkyl- or (2′-alkenyl)- or benzyl-sulfonyl]-benzothiazoles.
Tetrahedron Letters · 1991 · 378 citations
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