In the method, a trione compound represented by the following formula (1) is (i) reduced by NaAlH.sub.2(OCH.sub.2CH.sub.2OCH.sub.3).sub.2 and subsequently further reduced by a metal borohydride salt, or (ii) reduced by calcium borohydride, thereby producing an amide alcohol compound represented by the following formula (3) (wherein, R.sup.1 and R.sup.2 may be the same or different and each represents a hydrogen atom or a protecting group of an ureylene group; R.sup.4 represents an alkyl group, an aralkyl group, or an aryl group; and each of R.sup.5, R.sup.6, and R.sup.7 represents a hydrogen atom, an alkyl group, an alkoxy group, or a halogen atom).

##STR00001##

According to a nonaqueous electrolytic solution containing: a compound represented by General Formula (1); a solute; and a nonaqueous organic solvent, a nonaqueous electrolytic solution battery, and a compound represented by the General Formula (1), a nonaqueous electrolytic solution and a nonaqueous electrolytic solution battery having a low initial resistance value, and a compound that can be suitably used for the above nonaqueous electrolytic solution are provided.

##STR00001##

According to a nonaqueous electrolytic solution containing: a compound represented by General Formula (1); a solute; and a nonaqueous organic solvent, a nonaqueous electrolytic solution battery, and a compound represented by the General Formula (1), a nonaqueous electrolytic solution and a nonaqueous electrolytic solution battery having a low initial resistance value, and a compound that can be suitably used for the above nonaqueous electrolytic solution are provided.

##STR00001##

A process for producing a cyclic alkylene urea product of Formula I: ##STR00001## in which a compound of Formula II and/or Formula III is contacted in a reaction zone with a compound of Formula IV and/or Formula V and in the presence of one or more carbonyl delivering compounds; ##STR00002## wherein the compound of Formula II and/or the compound of Formula III are added to a reaction zone comprising compound of Formula IV and/or compound of Formula (V) continuously or semi-continuously over a period of time, or in two or more batches.

A process for producing a cyclic alkylene urea product of Formula I: ##STR00001## in which a compound of Formula II and/or Formula III is contacted in a reaction zone with a compound of Formula IV and/or Formula V and in the presence of one or more carbonyl delivering compounds; ##STR00002## wherein the compound of Formula II and/or the compound of Formula III are added to a reaction zone comprising compound of Formula IV and/or compound of Formula (V) continuously or semi-continuously over a period of time, or in two or more batches.

The invention relates to a compound of formula (I), wherein: A1 and A.sub.2 represent, independently of one another, a binding group comprising at least one nitrogen atom; Q.sub.1 and Q.sub.2 represent, independently of one another, a linkage group; and x is an integer between 2 and 6, preferably between 3 and 6. The invention also relates to a rubber composition comprising said compound.

The applicaton discloses pharmaceutical compounds of formula I useful for treating CNS diseases wherein m, s, R.sup.1R.sup.5, R.sup.6 and R.sup.7 are as defined herein.

##STR00001##

The applicaton discloses pharmaceutical compounds of formula I useful for treating CNS diseases wherein m, s, R.sup.1R.sup.5, R.sup.6 and R.sup.7 are as defined herein.

##STR00001##

Provided is a method for catalytically activating carbon dioxide as a carbonylation reagent with inorganic sulfur. In the method, carbon dioxide can be used to replace a toxic and harmful carbonylation reagent in the presence of H.sub.2S and an alkali for the synthesis of a carbonyl-containing fine chemical product. The method has a relatively high atomic economy and can reduce the generation of by-products.

The present invention relates to aryl sulfoxide derivatives, to the use thereof as acaricides and insecticides for controlling animal pests and to processes and intermediates for preparation thereof. The aryl sulfide and aryl sulfoxide derivatives have the general structure (I) ##STR00001##
in which the respective radicals are as defined in the description.