The masking of carbonyl groups by 1, 2-dimethyl-4, 5-di (mercaptomethyl) benzene
I Shahak, ED Bergmann
Index: Shahak,I.; Bergmann,E.D. Journal of the Chemical Society [Section] C: Organic, 1966 , p. 1005 - 1009
Full Text: HTML
Citation Number: 15
Abstract
Many aldehydes and ketones, as well as aldehydo-and keto-acid derivatives, give stable odourless crystalline thioacetals and thioketals with 1, 2-dimethyl-4, 5-di (mercaptomethyl) benzene (I). The rate of this condensation differentiates between aldehydes and ketones, and between α-keto-acids and other keto-acids. α-Hydroxy-methylene-ketones and-esters react with (I) in the their aldehyde forms. The derivatives of (I) with α-hydroxymethylene- ...
Related Articles:
Structure-reactivity relations for thiol-disulfide interchange
[Houk,J.; Whitesides,G.M. Journal of the American Chemical Society, 1987 , vol. 109, p. 6825]