Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Yuvaraj Arun"'
Autor:
Chennakesava Rao Kella, Chandrasekar Balachandran, Yuvaraj Arun, Easwaramoorthi Kaliyappan, Sakkarapalayam M. Mahalingam, Savarimuthu Ignacimuthu, Natarajan Arumugam, Abdulrahman I. Almansour, Raju Suresh Kumar, Paramasivan T. Perumal
Publikováno v:
Arabian Journal of Chemistry, Vol 13, Iss 12, Pp 9047-9057 (2020)
A Novel class of 1,4-disubstituted 1,2,3-triazoles have been synthesized in good to excellent yields via Cu(I) accelerated azide-alkyne click chemistry reaction strategy. The newly synthesized compounds were assessed for their in vitro antimicrobial
Externí odkaz:
https://doaj.org/article/445115270305406a82ff724b210f4bab
Publikováno v:
Pharmaceutics, Vol 14, Iss 7, p 1403 (2022)
Polyanhydrides have been synthesized for decades by melt-polycondensation of diacid monomers and 5 to >10 times mole excess acetic anhydride to diacid monomers to form polymers with a polydispersity ranging from 2.5 to 6 and low reproducibility. Hydr
Externí odkaz:
https://doaj.org/article/64bf530969ce4215970299362ac75173
Autor:
Sivakalai Mayakrishnan, Yuvaraj Arun, Chandrasekar Balachandran, Suresh Awale, Narayanan Uma Maheswari, Paramasivan Thirumalai Perumal
Publikováno v:
ACS Omega, Vol 2, Iss 6, Pp 2694-2705 (2017)
Externí odkaz:
https://doaj.org/article/8886a948efff46a4ba9ef61b8a81b0b4
Autor:
Kaliyappan Easwaramoorthi, Jeya A. Rajendran, Kella Chennakesava Rao, Chandrasekar Balachandran, Yuvaraj Arun, Sakkarapalayam M. Mahalingam, Natarajan Arumugam, Abdulrahman I. Almansour, Raju Suresh Kumar, Dhaifallah M. Al-thamili, Shin Aoki
Publikováno v:
Molecules, Vol 24, Iss 19, p 3501 (2019)
New 1,4-disubstituted β-pyrrolidino-1,2,3-triazoles were synthesized using a reusable copper-iodide-doped neutral alumina catalyst. Synthesis of diversely substituted triazoles and recyclability of CuI catalyst explains the broad scope of this proto
Externí odkaz:
https://doaj.org/article/037805d8f0d24e159b43073ef92409a3
Publikováno v:
Acta Crystallographica Section E, Vol 69, Iss 10, Pp o1585-o1585 (2013)
In the title compound, C26H20N4O2S, the central pyrrolidine ring adopts a twist conformation on the C—C bond involving the spiro C atom. Its mean plane makes dihedral angles of 78.83 (14), 65.91 (15) and 44.49 (18)° with the mean planes of the adj
Externí odkaz:
https://doaj.org/article/3d17b24ea13243a6896d4ea06c005aa8
Publikováno v:
Acta Crystallographica Section E, Vol 69, Iss 9, Pp o1481-o1481 (2013)
In the title compound, C25H20N6O2·0.15H2O, the dihedral angles between the least-squares planes of the indole and pyrrolidine rings and between the oxindole and imidazole rings are 77.66 (7) and 45.31 (7)°, respectively. The pyrrolidine ring and th
Externí odkaz:
https://doaj.org/article/2ba1482a70884ed4887149b5fb18523a
Publikováno v:
Acta Crystallographica Section E, Vol 69, Iss 8, Pp o1328-o1329 (2013)
In the title compound, C31H25N5O3·C2H6OS, the three indole/indoline units are all essentially planar with maximum deviations of 0.0172 (3), 0.053 (2) and 0.07 (2) Å. The pyrrolidine ring adopts an envelope conformation with the C atoms bearing the
Externí odkaz:
https://doaj.org/article/7e6fc60671604d98844e218cafb75e88
Publikováno v:
Acta Crystallographica Section E, Vol 68, Iss 7, Pp o2177-o2177 (2012)
The title compound, C24H29NO7, is asymmetric with a chiral centre located in the pyran ring and crystallizes as a racemate. The coumarin ring system and the fused pyran ring make a dihedral angle of 10.46 (8)°. A short intramolecular N—H...O hydro
Externí odkaz:
https://doaj.org/article/d6c7c3ef52ac450895fde2267a2fb50d
Publikováno v:
Acta Crystallographica Section E, Vol 67, Iss 11, Pp o2955-o2955 (2011)
The title compound, C20H21NO7, is asymmetric with a chiral centre located in the pyran ring and crystallizes as a racemate. The molecular framework is somewhat bent; the coumarin moiety and the pyran ring are inclined by 7.85 (5)°. The molecular str
Externí odkaz:
https://doaj.org/article/05f036f463914b0c92ba9a53b52e5017
Publikováno v:
Biomacromolecules. 23:3417-3428
The alternating architecture and hydrophobic side chains hinder hydrolytic cleavage and anhydride interchange in poly(sebacic acid-ricinoleic acid) (P(SA-RA)), which provides stable polyanhydrides at room temperature. In this report, a series of poly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93770bd0692bfca1b1d171315ceecc36
https://doi.org/10.1021/acs.biomac.2c00542
https://doi.org/10.1021/acs.biomac.2c00542