4.3 Article

Electrochemical bromolactonization of alkenoic acids with carbon tetrabromide: Synthesis of bromomethylated γ-lactones

Journal

SYNTHETIC COMMUNICATIONS
Volume 52, Issue 3, Pages 402-412

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/00397911.2022.2028843

Keywords

Alkenoic acids; bromolactonization; electrochemical reaction; gamma-lactones

Funding

  1. Soonchunhyang University
  2. Basic Science Research Program through the National Research Foundation of Korea [NRF-2021R1I1A3044807, 2021R1A6A1A03039503]
  3. National Research Foundation of Korea [2021R1A6A1A03039503] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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This study presents the development of an electrochemical method for bromination and cyclization reactions, which offers an environmentally friendly approach and enables efficient synthesis of bromomethylated gamma-lactone derivatives.
Electrochemical radical bromination and cyclization sequences of alkenoic acids developed in this study. This approach is environmental-friendly by using carbon tetrabromide as a bromine radical precursor. The electrochemical protocol offers a facile way to prepare bromomethylated gamma-lactones derivatives in moderate to high yields. [GRAPHICS] .

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