Organocatalytic Asymmetric Formal [3 + 2] Cycloaddition with in Situ-Generated N-Carbamoyl Nitrones
Author:
Affiliation:
1. Department of Organic Chemistry “A. Mangini”, University of Bologna, viale Risorgimento 4, 40136 Bologna, Italy
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja902458m
Reference28 articles.
1. For a recent review, see:Merino, P.InScience of Synthesis, Vol. 27;Padwa, A., Ed.Thieme:Stuttgart, Germany, 2004; p511.
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3. Catalytic enantioselective 1,3-dipolar cycloaddition reactions of nitrones
4. Lewis Acid Catalyzed Asymmetric Cycloadditions of Nitrones: α′-Hydroxy Enones as Efficient Reaction Partners
5. Enantioselective Nitrone Cycloadditions of α,β-Unsaturated 2-Acyl Imidazoles Catalyzed by Bis(oxazolinyl)pyridine−Cerium(IV) Triflate Complexes
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