This invention is directed to compound of Formula I and methods of using these compounds in the treatment of conditions in which modulation of a cathepsin, particularly cathepsin K or cathepsin L, will be therapeutically useful. ##STR00001##

The present invention relates to novel compounds having anti-cancer activity, methods of making these compounds, and their use for treating cancer and drug-resistant tumors, e.g. melanoma, metastatic melanoma, drug resistant melanoma, prostate cancer and drug resistant prostate cancer.

The present invention relates to novel compounds having anti-cancer activity, methods of making these compounds, and their use for treating cancer and drug-resistant tumors, e.g. melanoma, metastatic melanoma, drug resistant melanoma, prostate cancer and drug resistant prostate cancer.

The present invention relates to a process for preparing aldehydes and ketones by carbon-carbon bond cleavage of alkenes, wherein the process is catalysed by first row transition metal nitro coordinated polyoxometalate catalyst. The catalyst can be prepared by pre-treatment of aqua coordinated polyoxometalates with NO.sub.2, or they are formed in situ when the reactions are carried in nitroalkanes under aerobic conditions, or they are formed in situ from nitrosyl (NO) compounds in the presence of O.sub.2.

The present invention relates to a process for preparing aldehydes and ketones by carbon-carbon bond cleavage of alkenes, wherein the process is catalysed by first row transition metal nitro coordinated polyoxometalate catalyst. The catalyst can be prepared by pre-treatment of aqua coordinated polyoxometalates with NO.sub.2, or they are formed in situ when the reactions are carried in nitroalkanes under aerobic conditions, or they are formed in situ from nitrosyl (NO) compounds in the presence of O.sub.2.

The present disclosure relates to preparation of liquid salt including but not limiting to ionic liquid and applications thereof. More particularly, the present disclosure provides a process for preparing ionic liquid which comprises reacting at least one electron-pair acceptor and at least one electron-pair donor to form an adduct, and reacting the adduct with at least one electron-pair acceptor to prepare said salt. The present disclosure also provides for applications of the ionic liquid prepared in the present disclosure.

The present disclosure relates to preparation of liquid salt including but not limiting to ionic liquid and applications thereof. More particularly, the present disclosure provides a process for preparing ionic liquid which comprises reacting at least one electron-pair acceptor and at least one electron-pair donor to form an adduct, and reacting the adduct with at least one electron-pair acceptor to prepare said salt. The present disclosure also provides for applications of the ionic liquid prepared in the present disclosure.

A preparation method of carboxylic acids or ketones using ozone, singlet state oxygen atom O(.sup.1D) or hydroxyl free radical is provided. The method includes: filling ozone, singlet state oxygen atom O(.sup.1D) and/or hydroxyl free radical to cycloalkanes or benzenes at a pre-determined temperature and a pre-determined pressure in the presence or absence of light irradiation to produce carboxylic acids or ketones. The reaction occurs at room temperature and atmospheric pressure without producing harmful side products. The preparation method is a simple, low energy consuming, and eco-friendly method.

A preparation method of carboxylic acids or ketones using ozone, singlet state oxygen atom O(.sup.1D) or hydroxyl free radical is provided. The method includes: filling ozone, singlet state oxygen atom O(.sup.1D) and/or hydroxyl free radical to cycloalkanes or benzenes at a pre-determined temperature and a pre-determined pressure in the presence or absence of light irradiation to produce carboxylic acids or ketones. The reaction occurs at room temperature and atmospheric pressure without producing harmful side products. The preparation method is a simple, low energy consuming, and eco-friendly method.

The present disclosure provides an ionic liquid compound of Formula (I) and its application in reactions such as alkylation, arylation, acylation, diels alder and oligomerization, ##STR00001## The present disclosure also provides a process for preparing the ionic liquid compound of Formula (I) which involves preparing an ionic salt complex represented by Formula [(NR.sub.1R.sub.2R.sub.3).sub.iM.sub.1].sup.n+[X.sub.j].sup.n by mixing an amine represented by Formula NR.sub.1R.sub.2R.sub.3 and a metal salt represented by formula M.sub.1X.sub.j; and mixing the ionic salt complex and a metal salt represented by formula M.sub.2Y.sub.k to obtain the ionic liquid compound.