Methods of making compounds of Formula I are disclosed: ##STR00001##

The present invention refers to a process for a catalytic aryl transfer to rearrange the backbone of aromatic C—X bonds.

The present invention refers to a process for a catalytic aryl transfer to rearrange the backbone of aromatic C—X bonds.

Provide are a liquid crystal compound represented by formula I, and a liquid crystal mixture comprising the compound ##STR00001## A lateral trifluoromethyl-containing liquid crystal compound having the structural characteristics of Formula I not only has a negative dielectric anisotropy (Δε), an appropriate optical anisotropy (Δn), a higher clearing point (CP), a prominent low-temperature miscibility with other liquid crystals, and a low rotary viscosity (γ1), but also has a good stability to UV and high temperatures, particularly, a negative dielectric anisotropy. Same can be applied to the formulation of liquid crystal compositions of positive and negative types, and it is particularly prominent that same has the advantages of a good solubility at low temperatures and a high transmittance.

Provide are a liquid crystal compound represented by formula I, and a liquid crystal mixture comprising the compound ##STR00001## A lateral trifluoromethyl-containing liquid crystal compound having the structural characteristics of Formula I not only has a negative dielectric anisotropy (Δε), an appropriate optical anisotropy (Δn), a higher clearing point (CP), a prominent low-temperature miscibility with other liquid crystals, and a low rotary viscosity (γ1), but also has a good stability to UV and high temperatures, particularly, a negative dielectric anisotropy. Same can be applied to the formulation of liquid crystal compositions of positive and negative types, and it is particularly prominent that same has the advantages of a good solubility at low temperatures and a high transmittance.

In one aspect, the invention relates to compounds having the formula:

##STR00001##

where R.sup.1-R.sup.6, a, b, and Z are as defined in the specification, or a pharmaceutically acceptable salt thereof. These compounds have neprilysin inhibition activity. In another aspect, the invention relates to pharmaceutical compositions comprising such compounds; methods of using such compounds; and processes and intermediates for preparing such compounds.

In one aspect, the invention relates to compounds having the formula:

##STR00001##

where R.sup.1-R.sup.6, a, b, and Z are as defined in the specification, or a pharmaceutically acceptable salt thereof. These compounds have neprilysin inhibition activity. In another aspect, the invention relates to pharmaceutical compositions comprising such compounds; methods of using such compounds; and processes and intermediates for preparing such compounds.

Methods for stabilizing one or more peroxide compounds in solution comprising adding to the solution an effective amount of at least one compound selected from the group comprising (i) cyclic carbonates; (ii) poly-phosphonic acid chelating agents and salts thereof, and alkaline pH adjusting agents with a pKb value of up to 3.0, wherein the w/w ratio of the poly-phosphonic acid chelating agent or salt thereof to alkali or alkaline earth metal hydroxide is from about 1:1 to about 50:1; and (iii) mixtures thereof. Also disclosed are solutions comprising the above compounds, uses of the above compounds to stabilize peroxide compounds in solutions, and compounds recited above for use as novel stabilizers.

Methods for stabilizing one or more peroxide compounds in solution comprising adding to the solution an effective amount of at least one compound selected from the group comprising (i) cyclic carbonates; (ii) poly-phosphonic acid chelating agents and salts thereof, and alkaline pH adjusting agents with a pKb value of up to 3.0, wherein the w/w ratio of the poly-phosphonic acid chelating agent or salt thereof to alkali or alkaline earth metal hydroxide is from about 1:1 to about 50:1; and (iii) mixtures thereof. Also disclosed are solutions comprising the above compounds, uses of the above compounds to stabilize peroxide compounds in solutions, and compounds recited above for use as novel stabilizers.

The spontaneous orientation aid for a liquid crystal composition provides storage stability and allows liquid crystal molecules to be vertically aligned without a PI layer when added to a liquid crystal composition. When used in a liquid crystal composition, the spontaneous orientation aid can adsorb to substrates sandwiching a liquid crystal composition (liquid crystal layer) and keep the liquid crystal molecules aligned in a vertical direction. The spontaneous orientation aid makes it possible to align liquid crystal molecules without a PI layer (to induce vertical alignment of liquid crystal molecules under no applied voltage and to achieve horizontal alignment of the liquid crystal molecules under an applied voltage).