Palladium-Catalyzed Asymmetric [3+2] Cycloaddition of Trimethylenemethane with Imines
Author:
Affiliation:
1. Department of Chemistry, Stanford University, Stanford, California 94305-5080
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja0753389
Reference10 articles.
1. Pyrrole, pyrrolidine, pyridine, piperidine and tropane alkaloids (1998 to 1999)
2. Harwood, L. M.; Vickers, R. J. InSynthetic Applications of 1,3-DipolarCycloaddition Chemistry Toward Heterocycles and Natural Products; Padwa, A., Pearson, W. H., Eds.; John Wiley & Sons, Inc. New York, 2002; pp 169−252.
3. Reactions between trimethylenemethane metal complexes and the carbon–nitrogen double bond: nickel and palladium catalysed synthesis of pyrrolidines
4. A [3+2] cycloaddition and [4+3] cycloaddition approach to N-heterocycles via palladium-catalyzed TMM reactions with imines
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