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Wittig Ylide Mediated Decomposition of N-Sulfonylhydrazones to Sulfinates
Deepika Choudhary1, Vineeta Khatri1, Ashok K Basak1,2
1Department of Chemistry , University of Rajasthan , JLN Marg, Jaipur , 302004 , India.
Abstract:
N-Sulfonylhydrazones generate sulfinates selectively when treated with a stabilized Wittig ylide in a polar aprotic solvent at elevated temperature. The transition metal and base free decomposition method is applicable to N-sulfonylhydrazones generated from a number of aromatic and heteroaromatic aldehydes and ketones. In the case of N-tosylhydrazones derived from O-allyl and O-propargyl salicylaldehydes, selective formation of sulfinate occurs over intramolecular [3 + 2]-cycloaddition reaction.
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