Reduction of Benzophenones with SmI2. Post Electron Transfer Processes
Author:
Affiliation:
1. Department of Chemistry, Bar-Ilan University, Ramat-Gan 52900, Israel
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo802547r
Reference29 articles.
1. For some recent reviews, see:
2. Mechanistic Studies on the Roles of Cosolvents and Additives in Samarium(II)-Based Reductions
3. Samarium(II)-Iodide-Mediated Cyclizations in Natural Product Synthesis
4. Twenty-five years of organic chemistry with diiodosamarium: an overview
5. Recent developments in lanthanide mediated organic synthesis
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1. Atom economical coupling of benzophenone and N-heterocyclic aromatics with SmI2;Chemical Communications;2020
2. Intriguing multichannel photoinduced electron transfer in lanthanide(iii)–diphenylamine systems;Physical Chemistry Chemical Physics;2015
3. Mechanism of SmI2/Amine/H2O-Promoted Chemoselective Reductions of Carboxylic Acid Derivatives (Esters, Acids, and Amides) to Alcohols;The Journal of Organic Chemistry;2014-10-08
4. Ketyl-Type Radicals from Cyclic and Acyclic Esters are Stabilized by SmI2(H2O)n: The Role of SmI2(H2O)n in Post-Electron Transfer Steps;Journal of the American Chemical Society;2014-05-29
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