Stereoselective routes to functionalised hexa-2,4-dienals from cyclobutenes
Publication
, Journal Article
Ingham, S; Turner, RW; Wallace, TW
Published in: Journal of the Chemical Society, Chemical Communications
1985
Duke Scholars
Published In
Journal of the Chemical Society, Chemical Communications
DOI
ISSN
0022-4936
Publication Date
1985
Issue
23
Start / End Page
1664 / 1664
Publisher
Royal Society of Chemistry (RSC)
Citation
APA
Chicago
ICMJE
MLA
NLM
Ingham, S., Turner, R. W., & Wallace, T. W. (1985). Stereoselective routes to functionalised hexa-2,4-dienals from cyclobutenes. Journal of the Chemical Society, Chemical Communications, (23), 1664–1664. https://doi.org/10.1039/c39850001664
Ingham, Stephen, Ralph W. Turner, and Timothy W. Wallace. “Stereoselective routes to functionalised hexa-2,4-dienals from cyclobutenes.” Journal of the Chemical Society, Chemical Communications, no. 23 (1985): 1664–1664. https://doi.org/10.1039/c39850001664.
Ingham S, Turner RW, Wallace TW. Stereoselective routes to functionalised hexa-2,4-dienals from cyclobutenes. Journal of the Chemical Society, Chemical Communications. 1985;(23):1664–1664.
Ingham, Stephen, et al. “Stereoselective routes to functionalised hexa-2,4-dienals from cyclobutenes.” Journal of the Chemical Society, Chemical Communications, no. 23, Royal Society of Chemistry (RSC), 1985, pp. 1664–1664. Crossref, doi:10.1039/c39850001664.
Ingham S, Turner RW, Wallace TW. Stereoselective routes to functionalised hexa-2,4-dienals from cyclobutenes. Journal of the Chemical Society, Chemical Communications. Royal Society of Chemistry (RSC); 1985;(23):1664–1664.
Published In
Journal of the Chemical Society, Chemical Communications
DOI
ISSN
0022-4936
Publication Date
1985
Issue
23
Start / End Page
1664 / 1664
Publisher
Royal Society of Chemistry (RSC)