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Simple, catalytic C(sp3)-H azidation using the C-H donor as the limiting reagent.
Hooson, James F; Tran, Hai N; Bian, Kang-Jie; West, Julian G.
Affiliation
  • Hooson JF; Department of Chemistry, Rice University, 6500 Main St, Houston, TX, USA. jgwest@rice.edu.
  • Tran HN; Department of Chemistry, Rice University, 6500 Main St, Houston, TX, USA. jgwest@rice.edu.
  • Bian KJ; Department of Chemistry, Rice University, 6500 Main St, Houston, TX, USA. jgwest@rice.edu.
  • West JG; Department of Chemistry, Rice University, 6500 Main St, Houston, TX, USA. jgwest@rice.edu.
Chem Commun (Camb) ; 60(27): 3705-3708, 2024 Mar 28.
Article in En | MEDLINE | ID: mdl-38477139
ABSTRACT
C-N bonds play a critical role in pharmaceutical, agrochemical, and materials sciences, necessitating ever-better methods to forge this linkage. Here we report a simple procedure for direct C(sp3)-H azidation using iron or manganese catalysis and a nucleophilic azide source. All reagents are commercially available, the experimental procedure is simple, and we can use the C-H donor substrate as the limiting reagent, a challenge for many C-H azidation methods. Preliminary experiments are consistent with a hydrogen atom transfer (HAT)/radical ligand transfer (RLT) radical cascade mechanism and a wide variety of substrates can be azidated in moderate to high yields.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Chem Commun (Camb) Journal subject: QUIMICA Year: 2024 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Chem Commun (Camb) Journal subject: QUIMICA Year: 2024 Type: Article Affiliation country: United States