- Dendralenes
Dendralenes are discrete
acyclic cross-conjugatedpolyene s. The simplest dendralene isbutadiene (1) or [2] dendralene followed by [3] dendralene (2), [4] dendralene (3) and [5] dendralene (4) and so forth.The name "dendralene" is pulled together from the words
dendrimer ,linear andalkene . The higher dendralenes are of scientific interest because they open up a large array of neworganic compound s from a relatively simple precursor especially byDiels-Alder chemistry. Their cyclic counterparts are aptly calledradialene s. One synthetic route to [4] dendralene starts fromchloroprene . [cite journal | author = Alan D. Payne, Anthony C. Willis, and Michael S. Sherburn | year = 2005 | title = Practical Synthesis and Diels-Alder Chemistry of[4] Dendralene | journal = [http://pubs.acs.org/journals/jacsat/index.html Journal of the American Chemical Society] | volume = 127 | issue = 35 | pages = 12188–12189 | url = http://pubs3.acs.org/acs/journals/doilookup?in_doi=10.1021/ja053772%2b | accessdate = 2006-08-12 | doi = 10.1021/ja053772 | doi_brokendate = 2008-06-23 ] This compound is converted to aGrignard reagent by action ofmagnesium metal which is then reacted withcopper(I) chloride to anorganocopper intermediate which is in turn dimerized in anoxidative coupling reaction to thebutadiene dimer withcopper(II) chloride .[
Diels-Alder reactions
[4] dendralene shows a tandem
Diels-Alder reaction with thedienophile N-methyl-maleimide or NMM. Complete site selectivity is possible with the addition of thelewis acid methyldichloroaluminium. With one set of premixing and 2 equivalents of NMM the central diene group is targeted to the monoadduct 3. With another set and a larger amount of dienophile the terminal groups react and the reaction proceeds from the monoadduct to the trisadducts 2 and 2b.
[References
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