Reactions of Transition-Metal η1-Propargyl and η1-Allenyl Complexes with Sulfur Dioxide and Transition-Metal−Carbon Bond-Cleaving Reactions of the Cycloadducts Which Yield Cyclic Sulfenate Esters
journal contributionposted on 21.05.1998, 00:00 by Allison L. Hurley, Mark E. Welker, Cynthia S. Day
The preparation of several cyclopentadienyliron dicarbonyl η1-2-alkynyl and η1-allenyl complexes is reported. The 3 + 2 cycloaddition reactions of these complexes with sulfur dioxide yielded regioisomeric transition-metal-substituted 1,2-oxathiolen-1-yl oxides (sulfenate esters). One of the η1-allenyl complex SO2 cycloadducts has been characterized by X-ray crystallography. The transition metal can subsequently be cleaved from the sulfenate ester containing complexes under oxidative and nonoxidative reaction conditions to produce a variety of new sulfur-containing heterocycles.