Disclosed herein is a method for selectively reducing, using electrical energy, CO.sub.2 to formic acid, a catalyst for use in the method, and an electrochemical reduction system. The method for producing formic acid by electrochemically reducing carbon dioxide of the present invention includes (a) reacting carbon dioxide with a metal complex represented by formula (1), and (b) applying a voltage to a reaction product of the carbon dioxide and the metal complex represented by formula (1): ##STR00001##

Disclosed herein is a method for selectively reducing, using electrical energy, CO.sub.2 to formic acid, a catalyst for use in the method, and an electrochemical reduction system. The method for producing formic acid by electrochemically reducing carbon dioxide of the present invention includes (a) reacting carbon dioxide with a metal complex represented by formula (1), and (b) applying a voltage to a reaction product of the carbon dioxide and the metal complex represented by formula (1): ##STR00001##

An electrophotographic photosensitive member (1) includes a conductive substrate (2) and a photosensitive layer (3). The photosensitive layer (3) is a single-layer photosensitive layer containing at least a charge generating material, an electron transport material, a hole transport material, and a binder resin. The electron transport material includes a naphthoquinone derivative represented by general formula (1). An amount of triboelectric charge of calcium carbonate as measured by charging the calcium carbonate through friction with the photosensitive layer (3) is at least +7 C/g. In general formula (1), R.sup.11 and R.sup.12 are respectively the same as R.sup.11 and R.sup.12 described in the description. ##STR00001##

An electrophotographic photosensitive member (1) includes a conductive substrate (2) and a photosensitive layer (3). The photosensitive layer (3) is a single-layer photosensitive layer containing at least a charge generating material, an electron transport material, a hole transport material, and a binder resin. The electron transport material includes a naphthoquinone derivative represented by general formula (1). An amount of triboelectric charge of calcium carbonate as measured by charging the calcium carbonate through friction with the photosensitive layer (3) is at least +7 C/g. In general formula (1), R.sup.11 and R.sup.12 are respectively the same as R.sup.11 and R.sup.12 described in the description. ##STR00001##

This method for producing a fullerene derivative is a method for producing a fullerene derivative having a partial structure shown by formula (1) by reacting a predetermined halogenated compound and two carbon atoms adjacent to each other for forming a fullerene skeleton in a mixed solvent of an aromatic solvent and an aprotic polar solvent having a CO or SO bond in the presence of at least one metal selected from the group comprising manganese, iron, and zinc; ##STR00001## (in formula (1), C* are each carbon atoms adjacent to each other for forming a fullerene skeleton, A is a linking group having 1-4 carbon atoms for forming a ring structure with two C*, in which a portion thereof may be a substituted or condensed group).

This method for producing a fullerene derivative is a method for producing a fullerene derivative having a partial structure shown by formula (1) by reacting a predetermined halogenated compound and two carbon atoms adjacent to each other for forming a fullerene skeleton in a mixed solvent of an aromatic solvent and an aprotic polar solvent having a CO or SO bond in the presence of at least one metal selected from the group comprising manganese, iron, and zinc; ##STR00001## (in formula (1), C* are each carbon atoms adjacent to each other for forming a fullerene skeleton, A is a linking group having 1-4 carbon atoms for forming a ring structure with two C*, in which a portion thereof may be a substituted or condensed group).

Methods of selectively forming substituted pyrazines are provided. Methods of the present invention can include receiving a reaction solution including at least one carbon source and at least one nitrogen source, and heating the reaction solution to a reaction temperature and holding the reaction solution at the reaction temperature for a time sufficient to produce a reaction product comprising at least one substituted pyrazine. The carbon source can be selected from the group consisting of hydroxy ketone(s), sugar(s) treated with at least one buffer, and combinations thereof. Tobacco products incorporating substituted pyrazines are also provided.

Compounds of Formula I are disclosed

##STR00001##

As well as pharmaceutically acceptable salts thereof. Methods of using said compounds and pharmaceutical compositions containing said compounds are also disclosed.

Compounds of Formula I are disclosed

##STR00001##

As well as pharmaceutically acceptable salts thereof. Methods of using said compounds and pharmaceutical compositions containing said compounds are also disclosed.

Described herein are compounds that activate pyruvate kinase R, pharmaceutical compositions and methods of use thereof. These compounds are represented by Formula (I): wherein R.sup.1, R.sup.2, L.sup.1, and L.sup.2 are as defined herein. ##STR00001##