Efficient Synthesis of N-Alkylated α,β-Unsaturated Ketonitrones via Cu-Catalyzed Rearrangement
Author:
Affiliation:
1. Research and Analytical Center for Giant Molecules, Graduate School of Science, Tohoku University, Sendai 980-8578, Japan
2. Department of Chemistry, Graduate School of Science, Tohoku University, Sendai 980-8578, Japan
Funder
Ministry of Education, Culture, Sports, Science, and Technology
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol501889g
Reference34 articles.
1. Copper-Catalyzed Rearrangement ofN-Aryl Nitrones into Epoxyketimines
2. Diastereoselective Synthesis of C3-Quaternary Indolenines Using α,β-UnsaturatedN-Aryl Ketonitrones and Activated Alkynes
3. Reaction of aryl and alkyl nitro compounds with 2-butenylmagnesium chloride: synthesis of a new class of nitrones
4. A new rearrangement of nitrones: acid promoted conversion of vlnylnitrones into N-(γ-ketoalkyl)-N-phenylhydroxylamines
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