Intramolecular acylations of γ-benzoyloxy phosphine oxides: synthesis of optically active cyclopropyl ketones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Acyl transfer reactions with phosphine oxides: synthesis of E-homoallylic alcohols, cyclopropyl ketones, and γ-hydroxy ketones
2. Stereoselective acyl transfer reactions controlled by the diphenylphosphinoyl group: X-ray structures of stable crystalline silylated tetrahedral intermediates
3. Synthesis of potentially antiviral cyclopropyl nucleosides
4. Cyclopropane amino acids
5. Asymmetric dihydroxylations of allylic phosphine oxides
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1. A Concise Stereoselective Route to C- and P - Chirogenic Hydroxypropyl Phosphines by Ring-Opening of Optically Active Oxaphospholane-2-oxide;ChemistrySelect;2018-12-21
2. Base-Promoted Synthesis of β -Ketophosphine Oxides from Diphenylphosphorylallenes;Asian Journal of Organic Chemistry;2018-08-10
3. Base promoted synthesis of activated cyclopropanes bearing homologated carbonyl groups via tandem Michael addition–intramolecular enolate trapping;Organic & Biomolecular Chemistry;2011
4. ChemInform Abstract: Intramolecular Acylations of γ-Benzoyloxy Phosphine Oxides: Synthesis of Optically Active Cyclopropyl Ketones.;ChemInform;2010-08-05
5. The lithiation and acyl transfer reactions of phosphine oxides, sulfides and boranes in the synthesis of cyclopropanes;Organic & Biomolecular Chemistry;2009
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