Title
Generation of Molecular Complexity from Cyclooctatetraene Using Dienyliron and Olefin Metathesis Methodology
Grant Title
Natural Products Synthesis via Organoiron Methodology
Document Type
Article
Publication Date
5-2012
Source Publication
Organic and Biomolecular Chemistry
Source ISSN
1477-0520
Abstract
Transformation of the simple hydrocarbon cyclooctatetraene into a variety of polycyclic skeletons was achieved by sequential coordination to iron, reaction with electrophiles followed by allylated nucleophiles, decomplexation and olefin metathesis.
Recommended Citation
El-Mansy, Mohamed F.; Sar, Anobick; Chaudhury, Subhabrata; Wallock, Nathaniel J.; and Donaldson, William A., "Generation of Molecular Complexity from Cyclooctatetraene Using Dienyliron and Olefin Metathesis Methodology" (2012). Natural Products Synthesis via Organoiron Methodology. 2.
https://epublications.marquette.edu/data_nps/2
Document Rights and Citation of Original
Organic and Biomolecular Chemistry, Vol. 10 (May, 2012): 4844-4846. DOI: 10.1039/C2OB25636C.