37734-45-5Relevant articles and documents
S-alkyl chlorothioformates from xanthates
Gade, Alexandra M.,Abelt, Christopher J.
, p. 2097 - 2099 (2008/02/12)
Reaction of S-alkyl O-ethyl xanthates (S-alkyl O-ethyl dithiocarbonates) with catalytic Vilsmeier reagent generated in situ from N-formylmorpholine (morpholine-4-carbaldehyde) gives S-alkyl chlorothioformates in good yields. Georg Thieme Verlag Stuttgart.
Antipicornaviral compounds compositions containing them and methods for their use
-
, (2008/06/13)
Picornaviral 3C protease inhibitors, obtainable by chemical synthesis, inhibit or block the biological activity of the picornaviral 3C protease. These compounds, as well as pharmaceutical compositions that contain these compounds, are suitable for treatin
Antipicornaviral compounds and methods for their use and preparation
-
, (2008/06/13)
Picornaviral 3C protease inhibitors, obtainable by chemical synthesis, inhibit or block the biological activity of picornaviral 3C proteases. These compounds, as well as pharmaceutical compositions that contain these compounds, are suitable for treating patients or hosts infected with one or more picornaviruses. Several novel methods and intermediates can be used to prepare the novel picornaviral 3C protease inhibitors of the present invention.
Method for preparation of benzyl mercaptan
-
, (2008/06/13)
A method for the preparation of benzyl mercaptan is disclosed which comprises reacting a benzyl halide of the formula STR1 wherein X is chlorine or bromine, with an alkali metal hydrosulfide salt, at a temperature and for a sufficient period of time to ca
1-(N-Octylthiocarbonyl)-2-(4-thiazolyl)benzimidazole
-
, (2008/06/13)
New benzimidazoles substituted at the 1-position with carbonyl substituents and at the 2-position with a 4-thiazolyl group are effective fungicides and anthelmintics. The compounds as well as processes for their preparation are described along with antifungal and anthelmintic compositions for their use. The 1-position substituent is a hydrocarbon group of from 5 to 12 carbon atoms connected to the carbonyl group through an oxygen or a sulfur atom. The compounds are generally prepared by contacting a 1-unsubstituted benzimidazole with a hydrocarbon radical substituted chloroformate or chlorothiol formate.