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      Pd-Catalyzed C(sp(3))-H Carbonylation of Alkylamines: A Powerful Route to γ-Lactams and γ-Amino Acids.

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          Abstract

          A novel Pd-catalyzed direct C(sp(3))-H carbonylation of alkylamines for the synthesis of γ-lactams and γ-amino acids has been developed, in which TEMPO was used as the crucial sole oxidant. The synthetic prospect was demonstrated by the concise total synthesis of rac-Pregbalin.

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          Author and article information

          Journal
          Org. Lett.
          Organic letters
          American Chemical Society (ACS)
          1523-7052
          1523-7052
          Aug 07 2015
          : 17
          : 15
          Affiliations
          [1 ] †Department of Chemistry, University of Science and Technology of China, Hefei 230026, China.
          [2 ] ‡Key Laboratory of Synthetic and Self-Assembly Chemistry for Organic Functional Molecules, Chinese Academy of Sciences, Shanghai Institute of Organic Chemistry, Shanghai, 200032, China.
          Article
          10.1021/acs.orglett.5b01658
          26181629
          012d1956-8d2b-4410-a3ee-7dc444c4962c
          History

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