Zobrazeno 1 - 10
of 596
pro vyhledávání: '"S. Ravikanth"'
Autor:
Chapman, Edwin1 (AUTHOR) edwin.chapman@uzh.ch, West, Erin Ashley2 (AUTHOR) erin.west@kssg.ch, Kosnik, Mitja3,4 (AUTHOR) mitja.kosnik@klinika-golnik.si, Fischer, Nina Maria1 (AUTHOR) nfischer@vetclinics.uzh.ch, Favrot, Claude1 (AUTHOR) cfavrot@vetclinics.uzh.ch, Beeler, Leo5 (AUTHOR) leoserafino.beeler@uzh.ch, Rostaher, Ana1 (AUTHOR) arostaher@vetclinics.uzh.ch
Publikováno v:
Animals (2076-2615). Nov2024, Vol. 14 Issue 22, p3220. 12p.
Publikováno v:
Analytical Sciences. 22:1257-1260
A simple and rapid reversed-phase high-performance liquid-chromatographic method for the separation and determination of process-related impurities of celecoxib (CXB) in bulk drugs and pharmaceuticals was developed. The separation of impurities viz.,
Autor:
R. Yadla, S. Ravikanth, P. Shanthan Rao, V. V. V. N. S. RamaRao, Banda Narsaiah, D. Maitraie, G. Venkat Reddy
Publikováno v:
Tetrahedron. 60:12231-12237
Fluoro-substituted 3-cyano-2-methyl-benzo[b]furans and ethyl 2-methyl-benzo[b]furan-3-carboxylates are conveniently prepared in a single step in good yield by the microwave induced tandem intramolecular Wittig and Claisen rearrangement reactions of t
Autor:
R. Yadla, S. Ravikanth, G. Venkat Reddy, P. Shanthan Rao, V. V. V. N. S. Rama Rao, D. Maitraie
Publikováno v:
Synthetic Communications. 33:1523-1529
A rapid and efficient synthesis of acetylenic compounds by the microwave assisted intramolecular Wittig reaction of β-oxo-alkylidene-triphenylphosphoranes is reported. #IICT Communication No. 020106.
Autor:
Aravind, C. K.1,2,3 aravindck09@gmail.com, Priti, Hebbar1,3, Harikrishnan, S.4, Ravi, Chellam4, Afran, Parvez5, Padiyar, Ajith6, Thomas, Albin7, Sharma, Amatya8, Hegde, Amit9, Sayyed, Amit10, Krishnan, Aparna11, Arathy, S. Madhu12, Aithal, Aravinda13, Aravinda, H. R.14, Jain, Ayushi15, Banu, K. N. Prakash13, Bagali, Basanagoud16, Tapley, Benjamin17, Bhargavi, S. Shekar13, Phonde, Bhiku18
Publikováno v:
Scientific Reports. 8/15/2024, Vol. 14 Issue 1, p1-20. 20p.
Autor:
Muhmood, Azhar1,2,3 (AUTHOR) azharmuhmood@njau.edu.cn, Liu, Jianxin1,2,3 (AUTHOR) 20196307074@stu.njau.edu.cn, Liu, Dandan1,2,3 (AUTHOR) t2021062@njau.edu.cn, Liu, Shuiping1,2,3 (AUTHOR) liushuiping@hunau.edu.cn, Azzam, Mahmoud M.4 (AUTHOR) mazzam@ksu.edu.sa, Junaid, Muhammad Bilawal5 (AUTHOR) bilawallljunaid@gmail.com, Hou, Lili1,2,3 (AUTHOR) 2018207028@njau.edu.cn, Le, Guannan1,2,3 (AUTHOR) 2018107088@njau.edu.cn, Huang, Kehe1,2,3 (AUTHOR) khhuang@njau.edu.cn
Publikováno v:
Toxins. Aug2024, Vol. 16 Issue 8, p356. 14p.
Publikováno v:
2010 IEEE International Conference on Computational Intelligence and Computing Research.
The Human genome project raises the curtain to solve the Biological problems in much more sophisticated manner. The Biological data is huge and increasing at faster rate. The computational approach (Insilco) is much needed to analyze these huge biolo
Autor:
S. Ravikanth, D. Maitraie, Krishnan Ravikumar, Banda Narsaiah, G. Venkat Reddy, B. Sridhar, T. Yakaiah, K. V. N. S. Srinivas, P. Shanthan Rao
Publikováno v:
ChemInform. 37
Two strategies have been developed for the synthesis of novel quinazoline derivatives. 2,6-Dicyanoanilines were reacted with Grignard reagents followed by cyclization to give two quinazoline regioisomers 2 and 3. Alternately 2,6-dicyanoanilines on re
Autor:
P. Shanthan Rao, B. Sridhar, G. Venkat Reddy, S. Ravikanth, Krishnan Ravikumar, Banda Narsaiah, V. V. V. N. S. Rama Rao, D. Maitraie
Publikováno v:
ChemInform. 36
Synthesis of novel-2,3-bifunctionalised indole regioisomers ( 2 / 3 and 6 / 7 ) from unsymmetrical dicyanoanilines 1 by regioselective cyclization in two independent ways. Regioisomers 6 are further utilized in synthesis of novel 4,5-dihydro[1,3]oxaz
Autor:
P. Shanthan Rao, Banda Narsaiah, S. Ravikanth, G. Venkat Reddy, S. N. Reddy, D. Maitraie, R. Yadla, V. V. V. N. S. Rama Rao
Publikováno v:
ChemInform. 35
Unsymmetrical 1,2-phenylenediamine on reaction with various ketones resulted in a number of fluorinated heterocycles such as benzimidazoles, quinoxalines and spiro benzimidazoles in high yields. The role of substituents in diamine in its reaction wit