Rh(III)-Catalyzed [3 + 2] Annulation via C–H Activation: Direct Access to Trifluoromethyl-Substituted Indenamines and Aminoindanes
Author:
Affiliation:
1. Department of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research - Ahmedabad, Gandhinagar, Gujarat 382355, India
Funder
Department of Science and Technology, Ministry of Science and Technology
National Institute of Pharmaceutical Education and Research, Ahmedabad
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.9b00720
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1. Identification and Pharmacological Profile of an Indane Based Series of Ghrelin Receptor Full Agonists
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3. Cyclooxygenase-1-Selective Inhibitors Based on the (E)-2′-Des-methyl-sulindac Sulfide Scaffold
4. Differential Response of Estrogen Receptor Subtypes to 1,3-Diarylindene and 2,3-Diarylindene Ligands
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