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Intramolecular diels-alder cycloadditions of substituted furfuryl E-2-(phenylsulfonyl)acrylates
Affiliation:1. Otto Diels Institute of Organic Chemistry, Christiana Albertina University of Kiel, Otto-Hahn-Platz 3/4, Kiel D-24118, Germany;2. Glycogroup, Institute of Organic Chemistry, Technical University Graz, Stremayrgasse 9, Graz A-8010, Austria;1. Tumor Immunology and Gene Therapy Center, Eastern Hepatobiliary Surgery Hospital, The Second Military Medical University, Shanghai, China;2. Department of Comprehensive Treatment, Eastern Hepatobiliary Surgery Hospital, The Second Military Medical University, Shanghai, China;3. Oncology Department, Ji''an Hospital, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, China;1. Pharmacogenomics and Drug Development Group, Discipline of Pharmacology, School of Medical Sciences, Sydney Medical School, University of Sydney, NSW 2006, Australia;2. Centre for Pharmacology and Therapeutics, Division of Experimental Medicine, Imperial College London, Hammersmith Campus, United Kingdom;3. School of Mathematical and Physical Sciences, Faculty of Science, University of Technology Sydney, Ultimo, NSW 2007, Australia
Abstract:
Several substituted furfuryl E-2-(phenylsulfonyl)acrylates have been prepared by direct routes and cyclized in good yield under very mild conditions to give highly oxidized systems of potential use in natural products synthesis.
Keywords:
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