Tandem intramolecular Michael addition and 1,3-dipolar cycloaddition reactions of oximes; versatile new carbon-carbon bond forming methodology
Publication
, Journal Article
Armstrong, P; Grigg, R; Surendrakumar, S; Warnock, WJ
Published in: Journal of the Chemical Society Chemical Communications
January 1, 1987
Oximes undergo intramolecular Michael addition to proximate electronegative alkenes, generating cyclic nitrones which can be trapped inter- and intra-molecularly in 1,3-dipolar cycloaddition reactions taking place either separately or in tandem.
Duke Scholars
Published In
Journal of the Chemical Society Chemical Communications
DOI
ISSN
0022-4936
Publication Date
January 1, 1987
Issue
17
Start / End Page
1327 / 1328
Citation
APA
Chicago
ICMJE
MLA
NLM
Armstrong, P., Grigg, R., Surendrakumar, S., & Warnock, W. J. (1987). Tandem intramolecular Michael addition and 1,3-dipolar cycloaddition reactions of oximes; versatile new carbon-carbon bond forming methodology. Journal of the Chemical Society Chemical Communications, (17), 1327–1328. https://doi.org/10.1039/C39870001327
Armstrong, P., R. Grigg, S. Surendrakumar, and W. J. Warnock. “Tandem intramolecular Michael addition and 1,3-dipolar cycloaddition reactions of oximes; versatile new carbon-carbon bond forming methodology.” Journal of the Chemical Society Chemical Communications, no. 17 (January 1, 1987): 1327–28. https://doi.org/10.1039/C39870001327.
Armstrong P, Grigg R, Surendrakumar S, Warnock WJ. Tandem intramolecular Michael addition and 1,3-dipolar cycloaddition reactions of oximes; versatile new carbon-carbon bond forming methodology. Journal of the Chemical Society Chemical Communications. 1987 Jan 1;(17):1327–8.
Armstrong, P., et al. “Tandem intramolecular Michael addition and 1,3-dipolar cycloaddition reactions of oximes; versatile new carbon-carbon bond forming methodology.” Journal of the Chemical Society Chemical Communications, no. 17, Jan. 1987, pp. 1327–28. Scopus, doi:10.1039/C39870001327.
Armstrong P, Grigg R, Surendrakumar S, Warnock WJ. Tandem intramolecular Michael addition and 1,3-dipolar cycloaddition reactions of oximes; versatile new carbon-carbon bond forming methodology. Journal of the Chemical Society Chemical Communications. 1987 Jan 1;(17):1327–1328.
Published In
Journal of the Chemical Society Chemical Communications
DOI
ISSN
0022-4936
Publication Date
January 1, 1987
Issue
17
Start / End Page
1327 / 1328