Abstract:
The present invention relates to method for treating mycobacterial infection/disease by administration of a therapeutically effective amount of compound of formula I.
Abstract:
The present invention provides a process for the regioselective acylation of nucleosides, said process comprising preparing solution of a nucleoside, an acylating agent and a lipase; subjecting said solution to incubation at a predetermined temperature and filtering off the enzyme to obtain the product
Abstract:
The present invention relates to compounds of Formula (I): wherein- X and Y represent O, S, NR'; R n represents alkyl, aryl, OR 1 , NH 2 , SR 1 , NR 1 R 2 . wherein R 1 , R 2 = H, alkyl, phenyl, aryl, OCOR 3 , SCOR 3 , NHCOR 3 , NR 1 COR 3 , etc. (wherein R 3 represents alkyl, phenyl, aryl, heteroaryl); R' and R" represent H, alkyl, phenyl, substituted phenyl, phenyloxy, substituted phenyloxy, amino, monosubstitutedamino, disubstitutedamino, aryl, heteroaryl, aryloxy, heteroaryloxy, alkoxy, thioalkyl, thioalkyloxy, halo and a process for preparing the same.
Abstract:
The present invention relates to a dihydropyrimidinone compound of formula (I) wherein X represents O, S, etc. and R' represents alkyl, alkoxy, thioalkyl, thioalkyloxy, phenyl, substituted phenyl, phenyloxy, substituted phenyloxy, amino, monosubstitutedamino, disubstitutedamino, aryl, heteroaryl, aryloxy, heteroaryloxy, halo; R'' represents alkoxy, phenyloxy, substituted phenyloxy, aryloxy, heteroaryloxy, halo, NR 1 R 2 and R n represents OR 1 , NH 2 , SR 1 , NR 1 R 2 ; R 1 , R 2 = H, alkyl, phenyl, aryl, OCOR 3 , SCOR 3 , NHCOR 3 , NR 1 COR 3 ; R 3 represents alkyl, phenyl, aryl, heteroaryl.
Abstract:
The present invention provides a process for the regioselective acylation of nucleosides, said process comprising preparing solution of a nucleoside, an acylating agent and a lipase; subjecting said solution to incubation at a predetermined temperature and filtering off the enzyme to obtain the product