58928-29-3Relevant academic research and scientific papers
Acid-Catalyzed Synthesis of α-Trifluoromethylthiolated Carbonyl Compounds
Alazet, Sébastien,Ismalaj, Ermal,Glenadel, Quentin,Le Bars, Didier,Billard, Thierry
, p. 4607 - 4610 (2015)
The α-trifluoromethylthiolation of carbonyl compounds in soft acidic conditions has been developed. With this method only mono-trifluoromethylthiolation was selectively observed. Base-sensitive ketones can then be trifluoromethylthiolated. More sensitive
(Perhaloalkyl) thio-substituted aldehydes and ketones
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, (2008/06/13)
Perhaloalkanesulfenyl chlorides are reacted with aldehydes and ketones to provide novel (perhaloalkyl)thio-substituted aldehydes and ketones which are useful organic solvents and intermediates. As intermediates, these compounds are especially useful in the preparation of their carbamate derivatives which have pesticical utility.
