Chang‐Jung Wu
National Tsing Hua University(TW)
Publications by Year
Research Areas
Catalytic Alkyne Reactions, Synthetic Organic Chemistry Methods, Asymmetric Synthesis and Catalysis, Microbial Natural Products and Biosynthesis, Catalytic C–H Functionalization Methods
Most-Cited Works
- → Ruthenium-Catalyzed Aromatization of Enediynes via Highly Regioselective Nucleophilic Additions on a π-Alkyne Functionality. A Useful Method for the Synthesis of Functionalized Benzene Derivatives(2005)114 cited
- → Ruthenium-Catalyzed Regioselective 1,3-Methylene Transfer by Cleavage of Two Adjacent σ-Carbon−Carbon Bonds: An Easy and Selective Synthesis of Highly Subsituted Benzenes(2005)55 cited
- → Selective Synthesis of Chiral Dioxabicyclo[4.4.0]decane and Dioxabicyclo[5.3.0]decane from 3,4-Bisallyloxy-but-1-yne Derivatives via Ruthenium-Catalyzed En-yn-ene Metathesis(2003)38 cited
- → A New Co2(CO)8-Mediated Tandem [5 + 1]/[2 + 2 + 1]-Cycloaddition Reaction: A One-Pot Synthesis of Tricyclic δ-Lactones from cis-Epoxy Ene-ynes(2003)34 cited
- → Ruthenium‐Catalyzed Regioselective 1,3‐Methylene Transfer by Cleavage of Two Adjacent σ‐Carbon—Carbon Bonds: An Easy and Selective Synthesis of Highly Substituted Benzenes.(2005)3 cited
- → A New Co2(CO)8‐Mediated Tandem [5 + 1]/[2 + 2 + 1]‐Cycloaddition Reaction: A One‐Pot Synthesis of Tricyclic δ‐Lactones from cis‐Epoxy Ene‐ynes.(2003)
- → Ruthenium‐Catalyzed Aromatization of Enediynes via Highly Regioselective Nucleophilic Addition on a π‐Alkyne Functionality. A Useful Method for the Synthesis of Functionalized Benzene Derivatives.(2005)
- → Selective Synthesis of Chiral Dioxabicyclo[4.4.0]decane and Dioxabicyclo[5.3.0]decane from 3,4‐Bisallyloxy‐but‐1‐yne Derivatives via Ruthenium‐Catalyzed En‐yn‐ene Metathesis.(2004)