CH Bond Functionalization: Emerging Synthetic Tools for Natural Products and Pharmaceuticals
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Title
CH Bond Functionalization: Emerging Synthetic Tools for Natural Products and Pharmaceuticals
Authors
Keywords
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Journal
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 51, Issue 36, Pages 8960-9009
Publisher
Wiley
Online
2012-08-06
DOI
10.1002/anie.201201666
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- Enantioselective Synthesis of (+)-Cortistatin A, a Potent and Selective Inhibitor of Endothelial Cell Proliferation
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- Palladium(II)-Catalyzed Direct Arylation of Enaminones Using Organotrifluoroborates
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- 1,3-Diol Synthesis via Controlled, Radical-Mediated C−H Functionalization
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- Enantiospecific Total Synthesis of the Hapalindoles, Fischerindoles, and Welwitindolinonesviaa Redox Economic Approach
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- Synthesis of Benzocyclobutenes by Palladium-Catalyzed C−H Activation of Methyl Groups: Method and Mechanistic Study
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- Palladium-Catalyzed Direct C−H Arylation ofN-Iminopyridinium Ylides: Application to the Synthesis of (±)-Anabasine
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- Formal synthesis of (−)-morphine from d-glucal based on the cascade Claisen rearrangement
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