Zobrazeno 1 - 10
of 35
pro vyhledávání: '"M. G. Prabhudeva"'
Autor:
M. G. Prabhudeva, S. Naveen, K. R. Raghavendra, A. Dileep Kumar, Karthik Kumara, N. K. Lokanath, K. Ajay Kumar
Publikováno v:
IUCrData, Vol 2, Iss 1, p x162048 (2017)
In the title compound, C19H13Cl3N2S, the central dihydropyrazole ring adopts an envelope conformation with the chiral C atom as the flap. In the crystal, molecules are linked by weak C—H...Cl hydrogen bonds into supramolecular chains propagating al
Externí odkaz:
https://doaj.org/article/54a7489539ee4e98a5986564571018c2
Publikováno v:
IUCrData, Vol 2, Iss 1, p x170113 (2017)
The title compound, C38H40O8, possess an inversion centre at the centroid of the four-membered ring. The dihedral angle between the methylbenzene and trimethoxybenzene rings is 46.19 (8)°. In the crystal, molecules are linked via weak C—H...π int
Externí odkaz:
https://doaj.org/article/fbde21441c2642dca64779799b1f7009
Autor:
D. M. Lokeshwari, S. Naveen, M. G. Prabhudeva, K. R. Raghavendra, A. Dileep Kumar, N. K. Lokanath, K. Ajay Kumar
Publikováno v:
IUCrData, Vol 2, Iss 1, p x162013 (2017)
In the racemic title compound, C22H18Cl2N2O, the dihedral angles between the central dihydropyrazole ring (r.m.s. deviation = 0.018 Å) and the pendant methoxyphenyl, phenyl and dichlorophenyl rings are 3.96 (9), 15.90 (9) and 66.65 (9)° respectivel
Externí odkaz:
https://doaj.org/article/da63429d19e04db5b4ea1d1b6985de07
Publikováno v:
IUCrData, Vol 2, Iss 1, p x170038 (2017)
In the title compound, C14H11ClOS, the trans conformation of the C=C double bond in the central enone group is confirmed by the C—C=C—C torsion angle of 178.3 (4)°. The molecule is non-planar as seen by the dihedral angle of 22.6 (2)° between t
Externí odkaz:
https://doaj.org/article/a60596a3c2d14cc18f92de1899cf0169
Publikováno v:
IUCrData, Vol 1, Iss 12, p x161974 (2016)
In the title compound, C15H13ClOS, the olefinic double bond adopts an E configuration. The molecule is nearly planar, as seen by the dihedral angle of 9.07 (8)° between the thiophene and phenyl rings. The trans configuration of the C=C double bond i
Externí odkaz:
https://doaj.org/article/66ef291fbda1483fa57f3f55e76fc92d
Publikováno v:
Asian Journal of Chemistry. 32:2997-3001
This study demonstrates the efficient eco-friendly synthesis of a series of isoxazole derivatives 5a-h through (3+2) annulation of chalcones 3a-h and hydroxylamine (4) in citrus juice medium. The synthesized compounds were characterized by spectrosco
Autor:
Karthik Kumara, Achutha Dileep Kumar, Srinivasan Bharath, M. G. Prabhudeva, Neratur Krishnappagowda Lokanath, Kariyappa Ajay Kumar
Publikováno v:
Bioorganic Chemistry. 80:444-452
Inflammation-mediated disorders are on the rise and hence, there is an urgent need for the design and synthesis of new anti-inflammatory drugs with higher affinity and specificity for their potential targets. The current study presents an effective a
Autor:
Kariyappa Ajay Kumar, Mylarappa Ningappa, Neratur Krishnappagowda Lokanath, Karthik Kumara, Achutha Dileep Kumar, M. G. Prabhudeva
Publikováno v:
Research on Chemical Intermediates. 44:6453-6468
Increasing instances of antimicrobial drug resistance and Inflammation-mediated disorders requires the design and synthesis of new small-molecules with higher affinity and specificity for their potential targets to serve as antibiotics or anti-inflam
Publikováno v:
Current Chemistry Letters, Vol 7, Iss 3, Pp 73-80 (2018)
The current study presents the synthesis of thiophene-appended pyrazoles through 3+2 annulations of chalcones 3(a-g)with aryl hydrazine hydrochlorides 4(a-d) in acetic acid (30%) under reflux conditions produced the thiophene-pyrazole hybrids 5(a-g)
Autor:
Neratur Krishnappagowda Lokanath, M. G. Prabhudeva, K. M. L. Rai, H. K. Vivek, Kariyappa Ajay Kumar, C.B. Vagish, Karthik Kumara
Publikováno v:
Heliyon, Vol 7, Iss 7, Pp e07592-(2021)
Heliyon
Heliyon
In a sustained search for novel and effective antioxidants, a potential therapeutic leads against renal, and neurological disorders. Amongst the heterocycles, pyrazole and their derivatives have been extensively studied for their biological potencies