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Backbone‐Enabled Directional Peptide Macrocyclization through Late‐Stage Palladium‐Catalyzed δ‐C(sp<sup>2</sup>)−H Olefination
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The 67 checked references that resolve
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Palladium(II)‐Catalyzed Site‐Selective C(sp<sup>3</sup>)−H Alkynylation of Oligopeptides: A Linchpin Approach for Oligopeptide–Drug Conjugation
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Palladium(II)‐Catalyzed Site‐Selective C(sp<sup>3</sup>)−H Alkynylation of Oligopeptides: A Linchpin Approach for Oligopeptide–Drug Conjugation
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Palladium-Catalyzed Carbonylative Cyclization of Amines via γ-C(sp<sup>3</sup>)–H Activation: Late-Stage Diversification of Amino Acids and Peptides
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Internal Peptide Late‐Stage Diversification: Peptide‐Isosteric Triazoles for Primary and Secondary C(sp<sup>3</sup>)−H Activation
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Internal Peptide Late‐Stage Diversification: Peptide‐Isosteric Triazoles for Primary and Secondary C(sp<sup>3</sup>)−H Activation
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Site‐Selective δ‐C(sp<sup>3</sup>)−H Alkylation of Amino Acids and Peptides with Maleimides via a Six‐Membered Palladacycle
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Site‐Selective δ‐C(sp<sup>3</sup>)−H Alkylation of Amino Acids and Peptides with Maleimides via a Six‐Membered Palladacycle
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Constrained Cyclopeptides: Biaryl Formation through Pd‐Catalyzed C−H Activation in Peptides—Structural Control of the Cyclization vs. Cyclodimerization Outcome
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Manganese‐Catalyzed C−H Alkynylation: Expedient Peptide Synthesis and Modification
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Manganese‐Catalyzed C−H Alkynylation: Expedient Peptide Synthesis and Modification
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Rh(III)-Catalyzed Oxidative Coupling of Unactivated Alkenes via C−H Activation
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Bioorthogonal Diversification of Peptides through Selective Ruthenium(II)‐Catalyzed C–H Activation
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Bioorthogonal Diversification of Peptides through Selective Ruthenium(II)‐Catalyzed C–H Activation
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Total Synthesis of the Cyclopeptide Alkaloid Paliurine E. Insights into Macrocyclization by Ene−Enamide RCM
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