Synthesis of 3-Haloindoles via Cascade Oxidative Cyclization/Halogenation of 2-Alkenylanilines Mediated by PIDA and LiBr/KI
Author:
Affiliation:
1. School of Pharmaceutical Science and Technology, Tianjin University, Tianjin 300072, China
Funder
National Natural Science Foundation of China
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.2c02480
Reference66 articles.
1. The Combinatorial Synthesis of Bicyclic Privileged Structures or Privileged Substructures
2. Recent advances in indole syntheses: New routes for a classic target
3. Indole synthesis – something old, something new
4. Simple indole alkaloids and those with a nonrearranged monoterpenoid unit
5. Intramolecular Fischer Indole Synthesis for the Direct Synthesis of 3,4-Fused Tricyclic Indole and Application to the Total Synthesis of (−)-Aurantioclavine
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1. Synthesis of Selenocyanated Indoles via PhICl2‐Induced Electrophilic Intramolecular Cyclization of 2‐Alkynylanilines or 2‐Alkenylanilines;Asian Journal of Organic Chemistry;2024-01-25
2. Study of the Structure and Infrared Spectra of LiF, LiCl and LiBr Using Density Functional Theory (DFT);Materials;2023-07-30
3. K2S2O8-Promoted Consecutive Tandem Cyclization/Oxidative Halogenation: Access to 3-Halo-Pyrazolo[1,5-a]pyrimidines;ACS Omega;2023-06-22
4. Divergent electrosynthesis of 3-iodoindoles and indoles from 2-ethynylanilines under ambient and aqueous conditions;Organic Chemistry Frontiers;2023
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