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Discovery of SMD-6346: A Potent, Selective, and Orally Active SMARCA2 Degrader for Targeting SMARCA4-Deficient Human Cancers Click to copy article link Article link copied!
General Procedure A for the Synthesis of Compounds 9–23 General Step a and b To a solution of intermediate 33 (2.0 mmol, 1.0 equiv) in a DMF/DCE (1:1, 20 mL) mixture, aldehyde reagent 34 (3.0 mmol, 1.5 equiv) or acetone reagent 35 (4.0 mmol, 2.0 equiv) was added, followed by AcOH (0.2 mmol, 0.1 equiv) as a catalyst. The reaction mixture was stirred at room temperature overnight. Subsequently, NaBH(OAc)3 (4.0 mmol, 2.0 equiv) was added, and stirring continued for an additional 3 h.
Regioselective, Photocatalytic α-Functionalization of Amines
Download Hi-Res ImageDownload to MS-PowerPointCite This:J. Am. Chem. Soc. 2020, XXXX, XXX RETURN TO ARTICLES ASAPPREVCommunicationNEXT Lingying Leng Lingying Leng Department of Biochemistry, UT Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, Texas 75390-9038, United States , Yue Fu Yue Fu Department of Chemistry, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, United States , Peng Liu*, and Joseph M.
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