Enantioselective synthesis of dimethyl 3,4-diphenyladipate by electroreductive hydrocoupling of chiral N-trans-cinnamoyl-2-oxazolidones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. Cathodic reductive coupling of methyl cinnamate on boron-doped diamond electrodes and synthesis of new neolignan-type products;Beilstein Journal of Organic Chemistry;2015-02-03
2. 8.20 Partial Reduction of Enones, Styrenes, and Related Systems;Comprehensive Organic Synthesis II;2014
3. ChemInform Abstract: Enantioselective Synthesis of Dimethyl 3,4-Diphenyladipate by Electroreductive Hydrocoupling of Chiral N-trans-Cinnamoyl-2- oxazolidones.;ChemInform;2010-08-19
4. Stereoselective Oxidative and Reductive Coupling using Chiral Auxiliaries;Journal of Synthetic Organic Chemistry, Japan;2004
5. Stereoselective Hydrocoupling of Cinnamic Acid Esters by Electroreduction: Application to Asymmetric Synthesis of Hydrodimers;The Journal of Organic Chemistry;2002-10-26
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