| Literature DB >> 21976394 |
Henry Toombs-Ruane1, Nik Osinski, Thomas Fallon, Cindy Wills, Anthony C Willis, Michael N Paddon-Row, Michael S Sherburn.
Abstract
[3]Dendralene and [4]dendralene are converted smoothly into tricarbonyliron complexes. The structures of four complexes analyzed by DFT and single-crystal X-ray analysis show that, in contrast to free hydrocarbons, complexed dendralenes prefer a roughly in-plane conformation. The complexes are stable towards Fe(CO)(3) group migration up to 150 °C. The synthetic value of Fe(CO)(3) complexation in the dendralene series is demonstrated through a variety of selective synthetic manipulations (Diels-Alder reaction, dipolar cycloaddition, Simmons-Smith cyclopropanation, dihydroxylation, olefin cross metathesis) that are not achievable by direct transformation of the free hydrocarbons. Application to the synthesis of a previously unreported, highly reactive linear/cross-conjugated hydrocarbon is also described.Entities:
Year: 2011 PMID: 21976394 DOI: 10.1002/asia.201100455
Source DB: PubMed Journal: Chem Asian J ISSN: 1861-471X