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Hugo E. Gottlieb

Researcher at Bar-Ilan University

Publications -  197
Citations -  11805

Hugo E. Gottlieb is an academic researcher from Bar-Ilan University. The author has contributed to research in topics: Cycloaddition & Pericyclic reaction. The author has an hindex of 37, co-authored 196 publications receiving 10495 citations. Previous affiliations of Hugo E. Gottlieb include Instituto Biológico & Keele University.

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NMR Chemical Shifts of Common Laboratory Solvents as Trace Impurities.

TL;DR: 1H and 13C chemical shifts of what are, in the authors' experience, the most popular “extra peaks” in a variety of commonly used NMR solvents are collected, in the hope that this will be of assistance to the practicing chemist.
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NMR Chemical Shifts of Trace Impurities: Common Laboratory Solvents, Organics, and Gases in Deuterated Solvents Relevant to the Organometallic Chemist

TL;DR: Tables of 1H and 13C NMR chemical shifts have been compiled for common organic compounds often used as reagents or found as products or contaminants in deuterated organic solvents as discussed by the authors.
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Antioxidant activities and anthocyanin content of fresh fruits of common fig (Ficus carica L.)

TL;DR: Fruits of the Mission variety contained the highest levels of polyphenols, flavonoids, and anthocyanins and exhibited the highest antioxidant capacity.
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Electrolyte Solutions with a Wide Electrochemical Window for Rechargeable Magnesium Batteries

TL;DR: In this article, an electrolyte solution for rechargeable Mg batteries was developed, based on reaction products of phenyl magnesium chloride (PhMgCl) 2 -Alcl 3 and Alcl 3 Lewis acid in ethers.
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Electrolyte Solutions for Rechargeable Magnesium Batteries Based on Organomagnesium Chloroaluminate Complexes

TL;DR: In this paper, a variety of Mg(AX 4n R n R n ) 2 complexes, where A = Al, B, Sb, P, As, Fe, and Ta; X = Cl, Br, and F; and R = butyl, ethyl, phenyl, and benzyl (Bu, Et, Ph, and Bz, respectively) in several solvents, including tetrahydrofuran (THF), 2Me-THF, 1-3 dioxolane, diethyl ether, and poly