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Akbar Ali

Researcher at Government College University, Faisalabad

Publications -  129
Citations -  1915

Akbar Ali is an academic researcher from Government College University, Faisalabad. The author has contributed to research in topics: Natural bond orbital & Chemistry. The author has an hindex of 15, co-authored 109 publications receiving 925 citations. Previous affiliations of Akbar Ali include University of Sargodha & University of Vermont.

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First principles study of electronic and nonlinear optical properties of A–D–π–A and D–A–D–π–A configured compounds containing novel quinoline–carbazole derivatives

TL;DR: In this paper, a structural tailoring has been made at the donor and acceptor units of two recently synthesized quinoline-carbazole molecules (Q1, Q2) and two recently designed molecules Q1D1-Q1D3 and Q2D2-Q2D3 have been quantum chemically designed, respectively.
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An efficient one-pot strategy for the highly regioselective metal-free synthesis of 1,4-disubstituted-1,2,3-triazoles

TL;DR: A simple and efficient metal-free methodology for the regioselective synthesis of 1,4-disubstituted-1,2,3-triazoles has been developed by applying a novel inverse electron-demand-1-3-dipolar cycloaddition approach.
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Tris(trimethylsilyl)silane and visible-light irradiation: a new metal- and additive-free photochemical process for the synthesis of indoles and oxindoles

TL;DR: A combined tris(trimethylsilyl)silane and visible-light-promoted intramolecular reductive cyclization protocol for the synthesis of indoles and oxindoles has been developed and enables rapid and practical synthesis of functionalized nitrogen-based heterocycles in high yields under additive and metal-free, mild photochemical conditions.
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Efficient Synthesis, SC-XRD, and Theoretical Studies of O-Benzenesulfonylated Pyrimidines: Role of Noncovalent Interaction Influence in Their Supramolecular Network.

TL;DR: The theoretical-based study exhibited that both AMPBS and DAPBS compounds contain promising NLO features, and the Hirshfeld surface study showed that C–H···O, N–H·N, and especially C–h···C hydrogen bond interactions are the key contributors to the intermolecular stabilization in the crystal.