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Umer Rashid

Researcher at Universiti Putra Malaysia

Publications -  410
Citations -  14133

Umer Rashid is an academic researcher from Universiti Putra Malaysia. The author has contributed to research in topics: Catalysis & Biodiesel. The author has an hindex of 51, co-authored 381 publications receiving 10081 citations. Previous affiliations of Umer Rashid include University of Gujrat & Universiti Teknologi Petronas.

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Optimization of polyol ester production by transesterification of Jatropha-based methyl ester with trimethylolpropane using Taguchi design of experiment

TL;DR: In this article, the effects of temperature, pressure, ratio of JOME:TMP and catalyst amount were studied in optimization experiment, using Taguchi L9 experimental layout, and the optimum reaction conditions were identified to be 483 K, 25 kPa; 1.0% w/w catalyst and JOME-TMP molar ratio of 4:1.
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Physicochemical composition of hydro-distilled essential oil from coriander ( Coriandrum sativum L.) seeds cultivated in Pakistan

TL;DR: In this article, the physicochemical properties of the essential oil derived from the seeds of coriander (Coriandrum sativum) cultivated in Pakistan were analyzed using GC-FID and GC-MS.
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Synthesis of Biodiesel through Catalytic Transesterification of Various Feedstocks using Fast Solvothermal Technology: A Critical Review

TL;DR: In this article, the authors proposed microwave irradiation to speed up the reaction time of chemical reactions of biodiesel, which results in high yields of product in a shorter chemical reaction time.
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Solid-phase synthesis and biological evaluation of a parallel library of 2,3-dihydro-1,5-benzothiazepines.

TL;DR: Solid-phase synthesis of a parallel library of 3'-hydroxy-2,3-dihydrobenzothiazepines has been carried out through [4+3] annulation of alpha,beta-unsaturated ketones with aminothiophenol, using Wang resin as solid support to reflect a strong exploratory potential in search of new benzothiazepine as source of anticancer agents.
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Synthesis, crystal structure determination, biological screening and docking studies of N 1 -substituted derivatives of 2,3-dihydroquinazolin-4(1 H )-one as inhibitors of cholinesterases

TL;DR: The synthesized compounds have established a structural foundation for the design of new inhibitors of cholinesterase and Computational predictions of ADMET studies reveal that all the compounds have good pharmacokinetic properties with no AMES toxicity and carcinogenicity.