Structure Ligation Relationship of Amino Acids for the Selective Indole C−H Arylation Reaction: L‐Aspartic acid as Sustainable Alternative of Phosphine Ligands-Reference-Cited by-同舟云学术

Structure Ligation Relationship of Amino Acids for the Selective Indole C−H Arylation Reaction: L‐Aspartic acid as Sustainable Alternative of Phosphine Ligands

Published:2020-06-03 Issue:14 Volume:362 Page:2857-2863
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Lokhande† Shyam Kumar¹,Vaidya† Gargi Nikhil¹,Satpute Dinesh Parshuram¹,Venkatesh Ashwini¹,Kumar Sanjeev¹,Kumar Dinesh¹

Affiliation:

1. Department of Medicinal ChemistryNational Institute of Pharmaceutical Education and Research (NIPER) – Ahmedabad, Palaj Gandhinagar 382355, Gujarat India

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.202000426

Reference83 articles.

2. The mechanism of palladium(II)-mediated C–H cleavage with mono-N-protected amino acid (MPAA) ligands: origins of rate acceleration

3. Versatile reactivity of Pd-catalysts: mechanistic features of the mono-N-protected amino acid ligand and cesium-halide base in Pd-catalyzed C–H bond functionalization

4. Developing Ligands for Palladium(II)-Catalyzed C–H Functionalization: Intimate Dialogue between Ligand and Substrate

5. Transient Ligand‐Enabled Transition Metal‐Catalyzed C−H Functionalization

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