Zobrazeno 1 - 10
of 171
pro vyhledávání: '"Ratnasamy Somanathan"'
Publikováno v:
ARKIVOC, Vol 2017, Iss 4, Pp 194-209 (2017)
Externí odkaz:
https://doaj.org/article/8714d522b8d440c7b9f0a47e1dda3f6b
Autor:
Norma Aidé Cortez, Celia Z. Flores-López, Ramón Rodríguez-Apodaca, Lucía Z. Flores-López, Miguel Parra-Hake, Ratnasamy Somanathan
Publikováno v:
ARKIVOC, Vol 2005, Iss 6, Pp 162-171 (2005)
Externí odkaz:
https://doaj.org/article/280399e74d2644de9f7dc957025f19df
Autor:
Ángeles Gama, Lucía Z. Flores-López, Gerardo Aguirre, Miguel Parra-Hake, Lars H. Hellberg, Ratnasamy Somanathan
Publikováno v:
ARKIVOC, Vol 2003, Iss 11, Pp 4-15 (2003)
Externí odkaz:
https://doaj.org/article/0e446aa1ef93477fb329b6d1d41c28db
Publikováno v:
Acta Crystallographica Section E, Vol 70, Iss 8, Pp o878-o878 (2014)
The title compound, C21H24N4O2, is a potent serotonin 5-HT2 and α1-adrenoceptor antagonist. The n-propyl chain links the quinazolinedione heterocycle and the phenylpiperazine group in which the benzene ring is equatorially located and the piperazine
Externí odkaz:
https://doaj.org/article/54fc930c470049f4ba617709618828d0
Publikováno v:
Acta Crystallographica Section E, Vol 69, Iss 10, Pp o1519-o1519 (2013)
The title compound, C9H3F5O2, crystallizes as O—H...O hydrogen-bonded carboxylic acid dimers that, together with C—H...F interactions and O...F [2.8065 (13) and 2.9628 (13) Å] and F...F [2.6665 (11), 2.7049 (12) and 2.7314 (12) Å] contacts, for
Externí odkaz:
https://doaj.org/article/7c51bdaa167d4a2baf287e4b23711288
Autor:
Harold, Cruz, Felipe A, Servín, Gerardo, Aguirre, Sergio, Pérez, Domingo, Madrigal, Daniel, Chávez, Andrew L, Cooksy, Ratnasamy, Somanathan
Publikováno v:
ChiralityREFERENCES. 34(6)
We report herein the synthesis and application of enantiopure C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::63c950b8be70a7fcddfe7f9e40d5bcaf
https://pubmed.ncbi.nlm.nih.gov/35303374
https://pubmed.ncbi.nlm.nih.gov/35303374
Autor:
Ratnasamy Somanathan, Maximiliano de la Higuera Macías, Haydee Rojas Cabrera, Gabriela Huelgas, Cecilia Anaya de Parrodi, Rocío Sabala, Alejandra Domínguez-Huerta, Julio M. Hernández Pérez
Publikováno v:
ChiralityREFERENCES. 33(1)
In this study, the novel bifunctional homochiral thiourea-L-prolinamides 1-4, tertiary amino-L-prolinamide 5, and bis-L-prolinamides 6 and 7 were prepared from enantiomerically pure (11R,12R)-11,12-diamino-9,10-dihydro-9,10-ethanoanthracene 8 and (11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99f7c237c185317ff11e16e3d55772b7
https://pubmed.ncbi.nlm.nih.gov/33232537
https://pubmed.ncbi.nlm.nih.gov/33232537
Autor:
I. R. Jack, Salaheddine Boukhssas, Younas Aouine, Hassane Faraj, O. P. Chimankar, S. A. Osemeahon, Oumaima Karai, Peter Kovacic, K. O. Orubite, J. J. Lagowski, Khadim Dioukhane, Ratnasamy Somanathan, A. F. M. Fahmy, Anouar Alami, A. J. Hotton, Saïd Achamlale, Sara Hajib, A. Gandhe, Abdelilah El Hallaoui, J. T. Barminas, A. R. Bansod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a54c86824c9820843986746c8f7e5376
https://doi.org/10.9734/bpi/tac/v4
https://doi.org/10.9734/bpi/tac/v4
Publikováno v:
Journal of Applied Toxicology. 39:16-26
The industry of nanotechnology has had a rapid development in the last decades. In particular, silver nanoparticles (AgNPs) have unique properties so they can be used in different industrial applications, mainly in areas such as electronics, environm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70d1304e210a472ea46a6a52f965db2e
https://doi.org/10.1002/jat.3654
https://doi.org/10.1002/jat.3654
Autor:
Daniel Chávez, Domingo Madrigal, Ratnasamy Somanathan, Andrew L. Cooksy, Sergio Perez-Sicairos, Harold Cruz, Gerardo Aguirre, Felipe A. Servín
Publikováno v:
Chirality. 30:1036-1044
Herein, we report the synthesis of C2 -symmetric sulfonamides as homogeneous and heterogeneous organocatalysts and their application in the enantioselective conjugate 1,4-Michael addition of carbonylic nucleophiles to β-nitrostyrene. Organocatalysts
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4db951480ba7b86784ad718c984d781b
https://doi.org/10.1002/chir.22984
https://doi.org/10.1002/chir.22984