4.6 Review

Electrocatalysis as a key strategy for the total synthesis of natural products

Journal

ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 20, Issue 4, Pages 727-748

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ob02115j

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Funding

  1. SERB [CRG/2019/000113, STR/2020/000061]
  2. CSIR, New Delhi
  3. IISER Bhopal

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Electrochemical strategies are becoming an important method for the synthesis of organic compounds, particularly in the synthesis of heterocyclic motifs, enabling a wide range of nonclassical bond disconnections. Anodic electrochemical oxidative strategies have been successfully utilized in the synthesis of various structurally intriguing natural products.
Electrochemical strategies have been a powerful approach for the synthesis of valuable intermediates, in particular heterocyclic motifs. Because of the mild nature, a wide range of nonclassical bond disconnections have been achieved via in situ-generated radical intermediates in a highly efficient manner. In particular, anodic electrochemical oxidative strategies have been utilized for the total synthesis of many structurally intriguing natural products. In this review article, we have discussed a number of total syntheses of structurally intriguing alkaloids and terpenoids in which electrochemical processes play an important role as a key methodology.

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