Construction of Racemic and Enantiopure Biaryl Unnatural Amino Acid Derivatives via Pd(II)‐Catalyzed Arylation of Unactivated Csp 3 −H Bonds
Author:
Affiliation:
1. Department of Chemical Sciences Indian Institute of Science Education and Research Mohali Knowledge City Sector 81 SAS Nagar, Mohali, Manauli P.O. Punjab 140306 India
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejoc.202100683
Reference123 articles.
1. For selected reviews dealing with biaryls see:
2. Aryl−Aryl Bond Formation One Century after the Discovery of the Ullmann Reaction
3. Biaryl synthesis with arenediazonium salts: cross-coupling, CH-arylation and annulation reactions
4. Upgrading Cross-Coupling Reactions for Biaryl Syntheses
5. Construction of Biologically Important Biaryl Scaffolds through Direct C–H Bond Activation: Advances and Prospects
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2. Fluorene and Fluorenone Unnatural Amino Acid Motifs via Diastereoselective Pd(II)‐Catalyzed sp3C−H Functionalization;European Journal of Organic Chemistry;2024-05-22
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4. Assembling of Polyaryls (Terphenyls, Tetraphenyls, Pentaphenyls, and Hexaphenyls) through Pd(II)‐catalyzed C−H Arylation of Biaryl Carboxamides with Iodobiaryls;Asian Journal of Organic Chemistry;2023-12-06
5. Pd‐Catalyzed Arylation and Benzylation of Tyrosine at the δ−C(sp2)−H and C(2) Positions: Expanding the Library of Unnatural Tyrosines;European Journal of Organic Chemistry;2023-07-18
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