Zobrazeno 1 - 10
of 46
pro vyhledávání: '"M. Bairagi"'
Autor:
Keshab M. Bairagi, Priyanka Pal, Subhrajyoti Bhandary, Katharigatta N. Venugopala, Deepak Chopra, Susanta K. Nayak
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 75, Iss 11, Pp 1712-1718 (2019)
In the title 1:1 cocrystal, C7H4ClNO4·C6H6N2O, nicotinamide (NIC) and 2-chloro-5-nitrobenzoic acid (CNBA) cocrystallize with one molecule each of NIC and CNBA in the asymmetric unit. In this structure, CNBA and NIC form hydrogen bonds through O—H.
Externí odkaz:
https://doaj.org/article/93af24429e724df78ddcb8466fb40518
Autor:
Kapil S. Ingle, Keshab M. Bairagi, Jyoti Swarup Thakur, Ranganathan Sathishkumar, Ramanaiah Chennuru, Bikash Baishya, Susanta K. Nayak
Publikováno v:
Crystal Growth & Design. 23:1755-1767
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c7572af3cb13f409d68d84db1ca246f
https://doi.org/10.1021/acs.cgd.2c01290
https://doi.org/10.1021/acs.cgd.2c01290
Autor:
Sandeep Chandrashekharappa, Keshab M. Bairagi, Mahendra K. Mohan, Katharigatta N. Venugopala, Susanta K. Nayak
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 74, Iss 10, Pp 1388-1391 (2018)
The title compound, C18H23FO5, was synthesized by reacting diethyl malonate with 1-(4-fluorophenyl)-3-methylbut-2-en-1-one. The molecule adopts a loose conformation stabilized by weak C—H...O and C—H...π interactions. In the crystal, the molecul
Externí odkaz:
https://doaj.org/article/9ae89952834641e4ab90372dc24a9840
Autor:
Keshab M. Bairagi, Vipin B. S. Kumar, Subhrajyoti Bhandary, Katharigatta N. Venugopala, Susanta K. Nayak
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 74, Iss 8, Pp 1130-1133 (2018)
The title compounds, 2-iodobenzamide, C7H6INO (I), and 2-iodo-N-phenylbenzamide, C13H10INO (II), were both synthesized from 2-iodobenzoic acid. In the crystal structure of (I), N—H...O and hydrogen bonds form two sets of closed rings, generating di
Externí odkaz:
https://doaj.org/article/d8b5d01e40184ed9af8e5e35eea28bba
Autor:
Sandeep Chandrashekharappa, Keshab M. Bairagi, Mahendra K. Mohan, Viresh Mohanlall, Kabange Kasumbwe, Katharigatta N. Venugopala, Susanta K. Nayak
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 74, Iss 6, Pp 868-870 (2018)
The title compound, C10H5BrF6O, synthesized via continuous stirring of 3,5-bis(trifluoromethyl) acetophenone with bromine in an acidic medium and concentrated under reduced pressure, crystallizes with four molecules in the unit cell (Z = 4) and one f
Externí odkaz:
https://doaj.org/article/6d07af090572432cae680379bc210bfd
Autor:
V. K. Hinge, M. Bairagi, N. Yadav, S. K. Joshi, B. D. Shrivastava, S. N. Jha, D. Bhattacharya, A. Gaur
Publikováno v:
X-Ray Spectrometry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9521a4af7bee84a8bed7add34b7e539e
https://doi.org/10.1002/xrs.3369
https://doi.org/10.1002/xrs.3369
Autor:
Keshab M. Bairagi, Katharigatta N. Venugopala, Pradip Kumar Mondal, Bharti Odhav, Susanta K. Nayak
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 72, Iss 9, Pp 1335-1338 (2016)
The title hydrate, C13H14N2O4·H2O, crystallizes with two formula units in the asymmetric unit (Z′ = 2). The dihedral angles between the planes of the tetrahydropyrimidine ring and the 4-hydroxyphenyl ring and ester group are 86.78 (4) and 6.81 (6)
Externí odkaz:
https://doaj.org/article/87709eb57def48ad8ee51afbde9f26a3
Publikováno v:
Journal of Molecular Structure
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf4a62a86c4a3718c8ee2d9c5166b349
Autor:
Deepak Chopra, Rohit Bhowal, Keshab M. Bairagi, Avantika Hasija, Osama I. Alwassil, Smital A. Mohurle, Katharigatta N. Venugopala, Susanta K. Nayak, Kapil S. Ingle
Publikováno v:
ChemPlusChem. 86:1167-1176
A solvent-assisted grinding method has been used to prepare co-crystals in substituted dihydropyrimidines (DHPM) that constitutes pharmacologically active compounds. These were characterized using FT-IR, PXRD, and single-crystal X-ray diffraction. In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cc1b33c40654080e2d07c5c0ff2c152
https://doi.org/10.1002/cplu.202100259
https://doi.org/10.1002/cplu.202100259
Autor:
Nancy S. Younis, Katharigatta N. Venugopala, Ekta Sangtani, Susanta K. Nayak, Hany Ezzat Khalil, Keshab M. Bairagi, Rajesh G. Gonnade, Promise Madu Emeka, Osama I. Alwassil
Publikováno v:
Medicinal Chemistry. 16:996-1003
Background: This research project is designed to identify the anti-diabetic effects of the newly synthesized compounds to conclude the perspective of consuming one or more of these new synthetic compounds for diabetes management. Introduction: A seri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2bd8e5b6b9759e074968e837f2c3789
https://doi.org/10.2174/1573406416666191227123048
https://doi.org/10.2174/1573406416666191227123048