scholarly journals Synthesis of quaternary nano‐intermetallic LaTi 2 Ni 5 Al 4 with its hydrogen encapsulation and inspection using lithium‐hydride cell

2020 ◽  
Vol 15 (3) ◽  
pp. 201-205
Author(s):  
Hassen Jaafar ◽  
Arij Dhiab ◽  
Chiheb Slama ◽  
Ines Sahli ◽  
Mohieddine Abdellaoui
Keyword(s):  
Lithium Hydride

NMR and electron microscopy studies on irradiated lithium hydride

1970 ◽  
Vol 8 (3) ◽  
pp. ii
Author(s):  
P.C. Souers ◽  
T. Imai ◽  
T.S. Blake ◽  
R.M. Penpraze ◽  
H.R. Leider
Keyword(s):  
Electron Microscopy ◽  
Lithium Hydride

scholarly journals Role of lithium hydride in tuning morphology and porosity of nanocarbons derived from CO2

2021 ◽  
pp. 100134
Author(s):  
Chengfu Zeng ◽  
Kai Wang ◽  
Liangbin Pan ◽  
Bo Li ◽  
Jiahui Li ◽  
...  
Keyword(s):  
Lithium Hydride

Spin-coupled valence bond study of the lithium hydride anion

1989 ◽  
Vol 85 (11) ◽  
pp. 1713 ◽  
Author(s):  
Michael J. Ford ◽  
David L. Cooper ◽  
Joseph Gerratt ◽  
Mario Raimondi
Keyword(s):  
Valence Bond ◽  
Lithium Hydride

Measuring Spectral Indices in a Critical Cylindrical Uranium System with a Lithium Hydride End Reflector

2020 ◽  
Vol 83 (8) ◽  
pp. 1151-1156
Author(s):  
A. A. Vayvod ◽  
S. S. Besov ◽  
A. A. Yudov ◽  
M. A. Demidenko ◽  
V. I. Litvin ◽  
...  
Keyword(s):  
Lithium Hydride ◽  
Spectral Indices

Linear Synthesis of {4-[(2-Alkoxy/aralkyloxy-3,5-dichlorophenyl)sulfonyl]-1-piperazinyl}(2-furyl)methanones as Possible Therapeutic Agents

2019 ◽  
Vol 41 (4) ◽  
pp. 685-685
Author(s):  
Muhammad Athar Abbasi Muhammad Athar Abbasi ◽  
Wajiha Khan Wajiha Khan ◽  
Aziz ur Rehman Aziz ur Rehman ◽  
Sabahat Zahra Siddiqui Sabahat Zahra Siddiqui ◽  
Ghulam Hussain Ghulam Hussain ◽  
...  
Keyword(s):  
Alkaline Medium ◽  
Inhibitory Activity ◽  
Substitution Reaction ◽  
Parent Compound ◽  
Ph Control ◽  
Therapeutic Agents ◽  
Lithium Hydride ◽  
Aqueous Alkaline Medium

In the present work, a series of {4-[(2-alkyloxy/aralkyloxy-3,5-dichlorophenyl)sulfonyl]-1-piperazinyl}(2-furyl)methanones was synthesized through a linear bi-step approach. The synthesis was initiated by the coupling of 2-furyl(1-piperazinyl)methanone (1) with 3,5-dichloro-2-hydroxybenzenesulfonyl chloride (2) under dynamic pH control in aqueous alkaline medium to form parent compound, {4-[(3,5-dichloro-2-hydroxyphenyl)sulfonyl]-1-piperazinyl}(2-furyl)methanone (3). Then, the O-substitution reaction on nucleophile 3 was carried out by treating it with different alkyl/aralkyl halides (4a-l) in the presence of lithium hydride (LiH) and N,N-dimethylformamide (DMF) to obtained the designed {4-[(2-alkoxy/aralkyloxy-3,5-dichlorophenyl)sulfonyl]-1-piperazinyl}(2-furyl)methanones (5a-l). These synthesized compounds were screened against α-glucosidase enzyme and some of them exhibited considerable inhibitory activity. Additionally, compounds were also evaluated for hemolytic and cytotoxic profile.

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