Highly Regioselective Cleavages and Iodinations of Cyclic Ethers Utilizing SmI2
Author:
Affiliation:
1. Department of Chemistry, Center for Molecular Design and Synthesis, Korea Advanced Institute of Science and Technology, Daejon, 305-701, Korea
2. Department of Chemistry, Woosuk University, Chonbuk 565-701, Korea kimyh@mail.kaist.ac.kr
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo020179r
Reference29 articles.
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3. Greene, T. W.; Wuts, P. G. M.Protective Groups in Organic Synthesis, 3rd ed.; Wiley: New York, 1999; p 23.
4. The Reaction of Tetrahydrofuran and 2,5-Dimethyltetrahydrofuran with Acyl Halides
5. Ferric chloride in acetic anhydide. Mild and versatile reagent for the cleavage of ethers
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