English Intern
    Prof. Dr. W. A. Schenk


    Nucleophilic methylene transfer to complexes of sulfur dioxide leads to the formation of metal-coordinated sulfene (thioformaldehyde-S,S-dioxide, H2C=SO2) (see above, Sulfur Oxides) [52, 62, 107]. The cationic ruthenium sulfene complexes are highly reactive electrophiles which add even weak nucleophiles such as Cl or even the "non-nucleophilic" base NEt(i-Pr)2 [52]. This high reactivity may be exploited in C–C coupling reactions with enamines or enolates [62, 88]. Demetalation of the coordinated sulfinate is achieved by alkylation at oxygen and substitution by acetonitrile [88]. By using chiral ruthenium complexes, this sequence can be developed into an enantioselective synthesis of functionalized sulfinic acid esters [100].


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