Results 81 to 90 of about 4,252 (145)

A minimal transcription factor network is sufficient to drive paclitaxel biosynthesis. [PDF]

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Muscarinic thioligands with cyclopentane nucleus

Bioorganic & Medicinal Chemistry, 1996
Some thio- and the benzoyl-derivatives of deoxamuscarine were synthesized and tested as muscarinic agonists using radioligand binding assays and functional tests. In comparison with deoxamuscarine, used as reference compound, no dimension/distance modification is tolerated for correct lipophilic pocket recognition.
A. PIERGENTILI   +6 more
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A study of the fragmentation of cyclopentane‐1,3‐diols and of cyclopentane‐1,2,4‐triols

Organic Mass Spectrometry, 1975
AbstractThe mass spectra of the two cyclopentane‐1,3‐diol and of the three cyclopentane‐1,2,4‐triol stereoisomers have been studied. Extensive deuterium labelling allows the detection of complex processes, especially for the elimination of water from the [M – H2OO]+· and [M]+· ions.
Gérard A. Singy, A. Buchs
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Measurements of Cohesion Hysteresis between Cyclopentane Hydrates in Liquid Cyclopentane

Energy & Fuels, 2013
We measured cohesion hysteresis between cyclopentane hydrate particles in liquid cyclopentane in the temperature range from −8 to 6 °C.
Nobuo Maeda   +5 more
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Decomposition of cyclopentane on Ni(755): peculiar decomposition behavior of cyclopentane

Surface Science Letters, 1993
Abstract Decomposition of cyclopentane on Ni(755) and −(111) has been investigated by temperature-programmed desorption (TPD). Adsorption of cyclopentane occurs on both surfaces by a precursor-mediated mechanism. On the (755) surface cyclopentane decomposes almost completely into adsorbed carbon and gaseous hydrogen while heating up from 123 to 573 K.
H. Kuramochi   +5 more
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Equilibrium of Hydrogen + Cyclopentane and Carbon Dioxide + Cyclopentane Binary Hydrates

Journal of Chemical & Engineering Data, 2008
Cyclopentane (CP) forms sII hydrates, in which CP only occupies the large cavities. Small gas molecules such as hydrogen and carbon dioxide can be encaged in the small cavities. However, there are no reported data on the equilibrium conditions of CP + H2 and CP + CO2 binary hydrates, which are essential to developing CO2 capturing or H2 enriching ...
J. S. Zhang, Jae W. Lee
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The pure rotational Raman spectrum of cyclopentane-d0 and cyclopentane-d10

Journal of Molecular Spectroscopy, 1963
The pure rotational Raman spectra of C5H10 and C5D10 were photographed under high dispersion in the 13th order of a 300 grooves/mm plane grating using the line Hg 4358 A for excitation. The spectra are quite weak and diffuse and resemble that of a symmetric top rotator.
Kurt Tanner, Alfons Weber
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Hydrate Equilibrium Conditions for Cyclopentane and a Quaternary Cyclopentane-Rich Mixture

Journal of Chemical & Engineering Data, 2001
Experimental data on hydrate formation of cyclopentane and a 98.40 mass % purity cyclopentane mixture containing three impurities (0.48 mass % pentane, 0.48 mass % 2-methyl butane, and 0.72 mass % 2-methyl propane) in water were measured. The measurements were carried out in a transparent sapphire cell (100-cm3 effective volume) by applying a pressure ...
Fan, SS, Liang, DQ, Guo, KH
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Infrared Spectra of Crystalline Cyclopentane and Cyclopentane-d10

The Journal of Chemical Physics, 1969
Infrared spectra of crystalline cyclopentane and cyclopentane-d10 have been measured at different temperatures between 4000 and 200 cm−1. Spectroscopic evidence shows that form I (− 120°C) and form II (− 140°C) have the same degree of disorder as the liquid. In the ordered crystal form III (− 180°C) the molecule has a rigid bent conformation.
V. Schettino   +2 more
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Cyclopentanes

2021
Jie Jack Li, Minmin Yang
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