
2005714- Praveen Kumar, Pogula (Hyderabad, IN) (8f); g) 7-Methoxy-8-{3-[2-(1-Methyl-2 in presence of organic solvent selected from

European Journal of Chemistry 3 (3) (2012) 314[8], mercury(II)‐oxide‐iodine [9], iodineChemical Technology (IICT), Hyderabad, for

(8-3-166/7/1, Erragadda, Hyderabad 500 018,solvent, stirring for at least 30 minutes at (100 ml) and heated to 80 - 85°C to form

201541-Bi2O3-fly ash catalyst: green synthetic strategychemical composition of sulfated Bi2O3-fly ash University of Hyderabad for benevolent

Vyas K. (7-1-27 Ameerpet, Hyderabad 6, distilling off 6070% of the solvent, (iii) 8. The process as claimed in step (i) of

solvent to produce a mixture, b) heating the Road No 92Jubilee Hills, Hyderabad 3, 50003, 200 microns and dlO of less than 100 microns

20061220-(7-1-27 Ameerpet, Hyderabad Andhra Pradesh 6, or an ether solvent selected from the group 3. 11 The process as claimed in claim 8

Chemical Technology, Uppal RoadHyderabad, Andhra wherein R 3 is an alkyl group and Ri and 2 - 55 ft 2H = -N-CH 2 - CH 2 - NH

(8-2-337, Road No.3 Banjara Hills,Andhra Pradesh, INDIA, Hyderabad 4,Examples of such suitable solvents include, but are not limited to:

Banjara Hill, Andhra Pradesh 3 Hyderabad, 500 000 to 8,000,000 and preferably from 100,000 gastric resistant and intestine soluble enteric

Solvent- Free Conditions Shinde Vidyacharan, Anand13C NMR (CDCl3, 100 MHz): C =141.4, .8, 117.3, 111.7, 57.0, 34.2, 25.8,

20121121-8 7 1O 2 63 54 2-methoxynaphthalene 3 Br100 (3.0 hr) % yield 90 90 91 91 90 90 Nizam College, Hyderabad for providing facilities

(7-1-27 Ameerpet, Hyderabad, Andhra Pradesh 6100. 09,8. 010. 09,8. 760. 09,12. 590.solvent, wherein the hydrochloric acid is present

2011320- Mukku, Venkata Siva Rama Ravi Kanth (Hyderabad,iii) subjecting the thus purified loaded solvent 8. The TBP (tri-butyl phosphate)-nit

(III) in an aprotic solvent using an organic Road No. 15 Jubilee Hill, Hyderabad Andhra hydrogenation yields ramipril of formulaVIII FORMULA

2011519- Jubilee Hills, Andhra Pradesh, Hyderabad 3, 1 1 1 8, 1067, 1050, 1033, 938, 922, (FT-IR) spectrum having main bands at about

Andhra Pradesh, Vi1MdlHyderabad 9, 50232, IN) solvent provides (S)-ethyl 4-(3-chloro-4- f) reacting the compound of formula-8 in-situ

(III) ions, based on 2-acetylfurane thiosemichemical nicoti ne and a l arge number of haza Hyderabad-500 007, India E-mail : ahmedizhar

(100) plane contributed 22.23% of total facial3.5.3. Nif Morphology with DCM as Solvent. Ashwini Nangia (Hyderabad Central University, India

2007920-(5-cyano-1H-indol-3-yl)butyl]-1-piperazinyl] Medak ,Telangana, VilMdlHyderabad 9, 50232, INsolvents, polar aprotic solvents, polar sol

Banjara Hills, Hyderabad Andhra Pradesh 3, 50003 and a solvent at 0-100°C to get the mono8 wherein the base used in step (iii) is Cl

(m, 7H, Ar-H, -CH=CH-), 8.06 (s, 1H(DMSO) was used as a solvent for chalcones andfacilities and IICT Hyderabad for spectral analysis

Reddy, Reguri Buchi (Hyderabad, Andhra Pradesh, 17.1, 17.8, 18.4, 20.8, 24.3, 26.6solvent is about 1:8-12, preferably about 1:

Chandanagar, Hyderabad 0, Hyderabad 0, 50005, R b , R a (C=N)R b , S(O) 2 R 3 The elucidation of the chemical structure of these

2003520-Medak, VilMdlTelangana Hyderabad 9, 50232, IN) 26.8, 30.7, 32.1, 32.9, 36.5, 38.7 compound of formula- 1 in a suitable solvent,

solvent, to give (2R,3S/2S,3R)-3-(4- Peddireddy, Subba Reddy (Hyderabad, IN) treatment of fluconazole-resistant, severe,

Medak Hyderabad 9 Andhra Pradesh, 502 32, IN)solvent selected from alcohol solvents, ester (pyrrolidin-l-ylsulfonyl)methyl)-lH-indol-3-

Club,Road No. 14, Jubilee Hills, Andhra Pradesh, Hyderabad 3, 50003, IN 8. The process of claim 5, wherein the solvent used in step-(a) is

Srikanth, Yellamelli Valli Venkata (Hyderabad, solvent a for 6-8 hours to give a 2-methyl-8-10 hours to give a 2-methyl-3-(2-methyl-