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http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_3/101021jo0264729/authorship/4
http://hub.abes.fr/acs/periodical/joceah/2006/volume_71/issue_19/101021jo061190k/authorship/1
http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_23/101021jo0157730/authorship/1
http://hub.abes.fr/acs/periodical/joceah/2004/volume_69/issue_22/101021jo048937w/authorship/1
http://hub.abes.fr/acs/periodical/joceah/2004/volume_69/issue_4/101021jo0353942/authorship/1
http://hub.abes.fr/acs/periodical/joceah/2000/volume_65/issue_18/101021jo005534x/authorship/1
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A Short Olefin Metathesis-Based Route to Enantiomerically PureArylated Dihydropyrans and α,β-Unsaturated δ-Valero Lactones
Ring-Closing Olefin Metathesis and RadicalCyclization as Competing Pathways
Combining Ring-Closing Metathesis and HydroformylationStrategies: A Novel Approach to Spirocyclic γ-Butyrolactones
Ruthenium-Catalyzed Olefin Metathesis Double-BondIsomerization Sequence
Stereoselective Syntheses of Enantiomerically Pure 2,5-disubstitutedDihydropyrans Based on Olefin Metathesis
Diastereoselective Ring-Closing Metathesis in the Synthesis ofDihydropyrans
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