Ziting Xu
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Ziting Xu has a total of 8 co-authors. Here are the top co-authors by number of shared publications:
- Chong Liu
Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, TX 79409, USA
3 shared publications - Haibo Ge
Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, TX 79409, USA
3 shared publications - Ke Yang
Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology School of Petrochemical Engineering Changzhou University Changzhou Jiangsu China
3 shared publications - Dan Yuan
Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology, School of Petrochemical Engineering, Changzhou University, Changzhou 213164, China
1 shared publication - Faith Herington
Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, TX 79409, USA
1 shared publication - Yang Zhou
Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology, School of Petrochemical Engineering, Changzhou University, Changzhou 213164, China
1 shared publication
Latest Publications
- Open Access
Palladium-Catalyzed Cascade Reactions for Synthesis of Heterocycles Initiated by C(sp3)–H Functionalization
Heterocycles are widely present in natural products, pharmaceuticals, and organic functional materials. In heterocycle synthesis, Pd-catalyzed cascade C–H functionalization has been regarded as one of the most powerful approaches due to its advantages in terms of high atom efficiency and readily available starting materials. In this review, we will briefly introduce the major advances in palladium-catalyzed cascade C(sp3)–H activation and annulation for constructing different types of heterocycles through inter- and intramolecular pathways from 2010 to 2023.
Open AccessPalladium-Catalyzed Cascade Reactions for Synthesis of Heterocycles Initiated by C(sp3)–H Functionalization
Heterocycles are widely present in natural products, pharmaceuticals, and organic functional materials. In heterocycle synthesis, Pd-catalyzed cascade C–H functionalization has been regarded as one of the most powerful approaches due to its advantages in terms of high atom efficiency and readily available starting materials. In this review, we will briefly introduce the major advances in palladium-catalyzed cascade C(sp3)–H activation and annulation for constructing different types of heterocycles through inter- and intramolecular pathways from 2010 to 2023.
- Open Access
Palladium-Catalyzed β-C(sp3)–H Bond Arylation of Tertiary Aldehydes Facilitated by 2-Pyridone Ligands
2-Pyridone ligand-facilitated palladium-catalyzed direct C–H bond functionalization via the transient directing group strategy has become an attractive topic. Here, we report a Pd-catalyzed direct β-C(sp3)–H arylation reaction of tertiary aliphatic aldehydes by using an α-amino acid as a transient directing group in combination with a 2-pyridone ligand.
Open AccessPalladium-Catalyzed β-C(sp3)–H Bond Arylation of Tertiary Aldehydes Facilitated by 2-Pyridone Ligands
2-Pyridone ligand-facilitated palladium-catalyzed direct C–H bond functionalization via the transient directing group strategy has become an attractive topic. Here, we report a Pd-catalyzed direct β-C(sp3)–H arylation reaction of tertiary aliphatic aldehydes by using an α-amino acid as a transient directing group in combination with a 2-pyridone ligand.
- Open Access
- 30 November 2023
- Published by MDPI AG in Preprints.org
Palladium-Catalyzed β-C(sp3)–H Bond Arylation of Tertiary Aldehydes Facilitated by 2-Pyridone Ligands
2-Pyridone ligand-facilitated palladium-catalyzed direct C–H bond functionalization via the transient directing group strategy has become an attractive topic. Here we report a Pd-catalyzed direct β-C(sp3) –H arylation reaction of tertiary aliphatic aldehydes by using an α-amino acid as a transient directing group in combination with a 2-pyridone ligand.
- 30 November 2023
- Published by MDPI AG in Preprints.org
Open AccessPalladium-Catalyzed β-C(sp3)–H Bond Arylation of Tertiary Aldehydes Facilitated by 2-Pyridone Ligands
2-Pyridone ligand-facilitated palladium-catalyzed direct C–H bond functionalization via the transient directing group strategy has become an attractive topic. Here we report a Pd-catalyzed direct β-C(sp3) –H arylation reaction of tertiary aliphatic aldehydes by using an α-amino acid as a transient directing group in combination with a 2-pyridone ligand.