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Pd(OH)2/C (Pearlman's Catalyst): A Highly Active Catalyst for Fukuyama, Sonogashira, and Suzuki Coupling Reactions | The Journal of Organic Chemistry
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Direct arylation of heteroaromatic substrate with Pearlman's catalyst. | Download Scientific Diagram
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Hydroxyl group deprotection reactions with Pd(OH)2/C: a convenient alternative to hydrogenolysis of benzyl ethers and acid hydrolysis of ketals | Semantic Scholar
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Scheme 7 Hydrosilylation of aldehydes catalyzed by a nickel PCP-pincer... | Download Scientific Diagram
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Pd(OH)2/C (Pearlman's Catalyst): A Highly Active Catalyst for Fukuyama, Sonogashira, and Suzuki Coupling Reactions | The Journal of Organic Chemistry
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Direct arylation of heteroaromatic substrate with Pearlman's catalyst. | Download Scientific Diagram
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Pd(OH)2/C (Pearlman's Catalyst): A Highly Active Catalyst for Fukuyama, Sonogashira, and Suzuki Coupling Reactions | The Journal of Organic Chemistry
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Elaboration of the ether cleaving ability and selectivity of the classical Pearlman's catalyst [Pd(OH)2/C]: concise synthesis of a precursor for a myo-inositol pyrophosphate - ScienceDirect
Pd(OH)2/C, a Practical and Efficient Catalyst for the Carboxylation of Benzylic Bromides with Carbon Monoxide
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Pd(OH)2/C, a Practical and Efficient Catalyst for the Carboxylation of Benzylic Bromides with Carbon Monoxide
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