Highly Stereoselective Synthesis of Novel α-Haloenamides via a Mild and Efficient Hydrohalogenation of Ynamides
Author:
Affiliation:
1. Department of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol0300266
Reference53 articles.
1. Recent advances in the chemistry of ynamines and ynamides
2. Reaction of Secondary Acetamides withN-Dichloromethylene-N,N-dimethylammonium Chloride
3. Concise and Stereoselective Synthesis of Enamides and Dienamides by a Titanium-Mediated Coupling Method
4. Synthesis of Cyclic Dienamide Using Ruthenium-Catalyzed Ring-Closing Metathesis of Ene-Ynamide
5. Stereoselective synthesis of alcohols. Part LV. Domino hydroformylation-allylboration-hydroformylation reactions to give trans-perhydropyrano[3,2-b]pyridine derivatives
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