Switching regiocontrol in 1-aryl-substituted cyclohexadienyliron complexes in a formal total synthesis of lycoramine
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference12 articles.
1. Total synthesis of racemic lycoramine
2. General methods for alkaloid synthesis. Total synthesis of racemic lycoramine
3. A short stereospecific synthesis of (dl)-lycoramine. Control of relative stereochemistry by dipole effects
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1. Metal-Catalyzed Asymmetric Michael Addition in Natural Product Synthesis;Chemistry - A European Journal;2016-12-19
2. Reactivity of acyclic (pentadienyl)iron(1+) cations with phosphonate stabilized nucleophiles: application to the synthesis of oxygenated metabolites of carvone;Tetrahedron;2016-02
3. Organoiron Chemistry;Organometallics in Synthesis;2013-08-01
4. Regiodirecting effects in difunctionalised tricarbonyl[(1,2,3,4,5-η)-cyclohexadienyl]iron(1+) salts: building blocks for alkaloids;Tetrahedron Letters;2013-01
5. Influencing the Balance between ipso and ω Nucleophile Addition to (1-Arylcyclohexadienyl)iron Intermediates in Alkaloid Synthesis;European Journal of Organic Chemistry;2012-07-26
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