Xiang‐Ping Hu
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View article: Chiral P,N,N-Ligands for Pd-Catalyzed Asymmetric Allylic Substitutions
Chiral P,N,N-Ligands for Pd-Catalyzed Asymmetric Allylic Substitutions Open
Chiral P,N,N-ligands are a new type of ligands developed in recent years, which have been widely used in asymmetric catalytic reactions.In this study, chiral P,N,N-ligands were applied to palladium-catalyzed asymmetric allylic substitution…
View article: CCDC 2184318: Experimental Crystal Structure Determination
CCDC 2184318: Experimental Crystal Structure Determination Open
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available …
View article: CCDC 1912653: Experimental Crystal Structure Determination
CCDC 1912653: Experimental Crystal Structure Determination Open
View article: Ir-catalyzed asymmetric hydrogenation of β-keto esters with chiral ferrocenyl P,N,N-ligands
Ir-catalyzed asymmetric hydrogenation of β-keto esters with chiral ferrocenyl P,N,N-ligands Open
The Ir-catalyzed asymmetric hydrogenation of β-keto esters with chiral ferrocenyl P,N,N-ligands has been developed, providing the corresponding β-hydroxy esters in good to excellent enantioselectivities.
View article: Desilylation‐Activated Propargylic Transformation: Enantioselective Copper‐Catalyzed [3+2] Cycloaddition of Propargylic Esters with β‐Naphthol or Phenol Derivatives
Desilylation‐Activated Propargylic Transformation: Enantioselective Copper‐Catalyzed [3+2] Cycloaddition of Propargylic Esters with β‐Naphthol or Phenol Derivatives Open
A copper‐catalyzed asymmetric [3+2] cycloaddition of 3‐trimethylsilylpropargylic esters with either β‐naphthols or electron‐rich phenols has been realized and proceeds by a desilylation‐activated process. Under the catalysis of Cu(OAc) 2 ⋅…
View article: CCDC 1499586: Experimental Crystal Structure Determination
CCDC 1499586: Experimental Crystal Structure Determination Open
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available …