Stereoselective Chlorination and Bromination of Enamides and Enamines via an Electrostatic Attraction Effect Using (1,1-Diacetoxyiodo)benzene and a Halide Source-Reference-Cited by-同舟云学术

Stereoselective Chlorination and Bromination of Enamides and Enamines via an Electrostatic Attraction Effect Using (1,1-Diacetoxyiodo)benzene and a Halide Source

Published:2015-10-07 Issue:20 Volume:80 Page:10000-10008
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Xing Linlin¹,Li Chunbao¹

Affiliation:

1. Department of Chemistry, School of Science, Tianjin University, Tianjin 300072, China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.5b01603

Reference60 articles.

1. Enamides: valuable organic substrates

2. Direct Metal‐Catalyzed Regioselective Functionalization of Enamides

3. Enamide Derivatives: Versatile Building Blocks for Highly Functionalized α,β-Substituted Amines

4. Enamide Derivatives: Versatile Building Blocks for Total Synthesis

5. Chemo- and stereoselective reduction of enaminones for the preparation of biologically active compounds

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