Reverse Cope Elimination of Hydroxylamines and Alkenes or Alkynes: Theoretical Investigation of Tether Length and Substituent Effects-Reference-Cited by-同舟云学术

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Reverse Cope Elimination of Hydroxylamines and Alkenes or Alkynes: Theoretical Investigation of Tether Length and Substituent Effects

Published:2012-01-17 Issue:4 Volume:134 Page:2434-2441
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Krenske Elizabeth H.,Davison Edwin C.¹,Forbes Ian T.²,Warner Jacqueline A.¹,Smith Adrian L.¹,Holmes Andrew B.¹³,Houk K. N.⁴

Affiliation:

1. Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, U.K.

2. GlaxoSmithKline, Gunnels Wood Road, Stevenage Herts SG1 2NY, U.K.

3. CSIRO Materials Science and Engineering, Bag 10, Clayton South, VIC 3169, Australia

4. Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095, United States

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja211568k

Reference91 articles.

1. Cyclization of unsaturated hydroxylamine derivatives

2. New synthesis of 2-alkylpyrrolidines and 2-alkylpiperidines

3. Nitrones and oxaziridines. XXII. Preparation and cyclization of some δ,ε-unsaturated hydroxylamines

4. The reverse Cope cyclisation: a classical reaction goes backwards

5. X = Y - ZH systems as potential 1,3-dipoles part 35. Generation of nitrones from oximes. Class 3 processes. Tandem intramolecular michael addition (1,3-azaprotio cyclotransfer) - intermolecular 1,3-dipolar cycloaddition reactions.

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