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Relevant bibliographies by topics / Decan

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Journal articles

Academic literature on the topic 'Decan'

Author: Grafiati

Published: 26 July 2024

Last updated: 27 July 2024

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Journal articles on the topic "Decan"

1

Aitken, R., Neil Keddie, and Alexandra Slawin. "3,5-Dithiatricyclo[5.2.1.02,6]decan-4-one." Molbank 2020, no. 2 (2020): M1126. http://dx.doi.org/10.3390/m1126.

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The X-ray structure of the title compound has been determined and the structure shows an exo-configured planar dithiolanone ring. This is in contrast to the few previous dithiolanones to be characterised crystallographically, which are all twisted.

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2

Graham, David B., Alexander L. Eastman, Kim N. Aldy, et al. "Outcomes and Long Term Follow-up after Emergent Cricothyroidotomy: Is Routine Conversion to Tracheostomy Necessary?" American Surgeon 77, no. 12 (2011): 1707–11. http://dx.doi.org/10.1177/000313481107701248.

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The purpose of this study is to identify factors associated with survival after cricothyroidotomy (CRIC), and to ascertain long-term outcomes in patients simply decannulated after CRIC versus those revised to tracheostomy. All CRICs between October 1, 1995 and June 20, 2010 were reviewed. Patients were contacted by phone, visited at their last known address, or queried in the Center for Disease Control's National Death Index. DECAN were those CRICs decannulated without revision. TRACH were those revised to a tracheostomy at any point. Ninety-five CRIC patients were identified. In 94 per cent o

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3

Polat, İlknur, Selçuk Eşsiz, Uğur Bozkaya, and Emine Salamci. "Efficient and regioselective synthesis of dihydroxy-substituted 2-aminocyclooctane-1-carboxylic acid and its bicyclic derivatives." Beilstein Journal of Organic Chemistry 18 (January 6, 2022): 77–85. http://dx.doi.org/10.3762/bjoc.18.7.

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The first synthesis of 2-amino-3,4-dihydroxycyclooctane-1-carboxylic acid, methyl 6-hydroxy-9-oxo-8-oxabicyclo[5.2.1]decan-10-yl)carbamate, and 10-amino-6-hydroxy-8-oxabicyclo[5.2.1]decan-9-one starting from cis-9-azabicyclo[6.2.0]dec-6-en-10-one is described. cis-9-Azabicyclo[6.2.0]dec-6-en-10-one was transformed into the corresponding amino ester and its protected amine. Oxidation of the double bond in the N-Boc-protected methyl 2-aminocyclooct-3-ene-1-carboxylate then delivered the targeted amino acid and its derivatives. Density-functional theory (DFT) computations were used to explain the

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4

Totchasov, E. D., M. Yu Nikiforov, and G. A. Al’per. "Heat capacity calculations for the decan-1-ol-n-decane system from viscosity data." Russian Journal of Physical Chemistry A 81, no. 8 (2007): 1346–48. http://dx.doi.org/10.1134/s0036024407080304.

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5

Polunkin, Ie V., V. S. Pilyavsky, T. M. Kamenieva, S. L. Melnykova, О. О. Gajdaj, and Yu I. Bogomolov. "Temperature inversion of the action of multilayer fullerenoid structures in the oxidation of N-decan by molecular oxygen." Catalysis and Petrochemistry, no. 32 (2021): 99–105. http://dx.doi.org/10.15407/kataliz2021.32.099.

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It was established that at low temperatures MFS inhibit the oxidation of n-decan, and at temperatures close to the boiling point of the hydrocarbon, on the contrary, accelerate the transformation of the original alkane molecules. The composition of alkane transformation products in the high-temperature two-phase (gas-liquid) oxidation regime was analyzed by gas-liquid chromatography. It is shown that the transformation of n-decan molecules occurs according to the same schemes both in the case of oxidation without the additive of MFS, and in the presence of these compounds in a liquid. The work

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6

Jänchen, Jochen, and Helmut Stoch. "Isostere Adsorptionsuntersuchungen von n-Decan an Silicalit." Zeitschrift für Chemie 24, no. 4 (2010): 158–59. http://dx.doi.org/10.1002/zfch.19840240435.

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7

Krech, F., K. Issleib, A. Zschunke, and H. Meyer. "Cis- und trans-1-Phosphabicyclo[4.4.0]decan." Zeitschrift f�r anorganische und allgemeine Chemie 553, no. 10 (1987): 136–46. http://dx.doi.org/10.1002/zaac.19875531016.

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8

Ha, Kwang. "Crystal structure of 2-(tricyclo[3.3.1.13,7]decan-1-yl)-3-(tricyclo[3.3.1.13,7]- decan-1-ylimino)isoindolin-1-one, C28H34N2O." Zeitschrift für Kristallographie - New Crystal Structures 228, no. 1 (2013): 107–8. http://dx.doi.org/10.1524/ncrs.2013.0070.

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Abstract C28H34N2O, triclinic, P1̄ (no. 2), a = 6.604(1) Å, b = 11.680(2) Å, c = 15.286(3) Å, α = 70.242(4)°, β = 87.390(4)°, γ = 81.377(4)°, V = 1097.1 Å3, Z = 2, Rgt(F) = 0.0546, wRref(F2) = 0.1604, T = 200 K.

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9

Ma, Yuguo, Emil B. Lobkovsky, and Geoffrey W. Coates. "Titanium(iv) catalysts with ancillary imino-spiroketonato ligands: synthesis, structure and olefin polymerization." Dalton Transactions 44, no. 27 (2015): 12265–72. http://dx.doi.org/10.1039/c5dt01104c.

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10

Hu, Gang, Chu Wang, Xin Xin, et al. "Design, synthesis and biological evaluation of novel 2,4-diaminopyrimidine derivatives as potent antitumor agents." New Journal of Chemistry 43, no. 25 (2019): 10190–202. http://dx.doi.org/10.1039/c9nj02154j.

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