Stereoselective cyclopropanation and ring-opening: Application to the synthesis of pure (S)-2-methyl-3-arylpropylamines
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference33 articles.
1. 3-Phenylpropylamine, eine neue Stoffklasse systemisch wirksamer Fungicide
2. Sterol metabolism in wheat treated byN-substituted morpholines
3. Chirality and Crop Protection
4. An Efficient Chemoenzymatic Synthesis of S-(-)-Fenpropimorph
5. Short chemoenzymatic synthesis of S-enantiomers of two systemic fungicides
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1. Chemo-, regio-, and diastereoselectivity preferences in the reaction of a sulfur ylide with a dienal and an enone;Organic & Biomolecular Chemistry;2011
2. ChemInform Abstract: Stereoselective Cyclopropanation and Ring-Opening: Application to the Synthesis of Pure (S)-2-Methyl-3-arylpropylamines.;ChemInform;2010-06-18
3. TheSonogashiraCoupling of Polymer-Supported Propargylamine with Aryl Iodides;Helvetica Chimica Acta;2010-01
4. Asymmetric cyclopropanation with diazoacetates induced by carbohydrate-derived chiral auxiliaries;Tetrahedron: Asymmetry;2007-06
5. Overview of the Separation of Agrochemical Enantiomers on Commercial CSPs;Journal of Liquid Chromatography & Related Technologies;2004-01
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