Results 61 to 70 of about 237 (72)
High-dose rocuronium-induced paralysis of the adductor pollicis muscle facilitates detection of the timing for tracheal intubation in elderly patients: a randomized double-blind study. [PDF]
J Anesth, 2020 Takagi S +7 more
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Potentiation of Rocuronium Bromide by Lithium Carbonate: A Case Report. [PDF]
Anesth Prog, 2020 Kishimoto N, Yoshikawa H, Seo K.
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Effect of body mass index and rocuronium on serum tryptase concentration during volatile general anesthesia: an observational study. [PDF]
Clinics (Sao Paulo), 2020 Kosciuczuk U, Knapp P, Jakubow P.
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A Case of Rocuronium-Induced Anaphylactic Shock in an Asthmatic Child. [PDF]
Anesth Prog, 2018 Tanoue R +3 more
europepmc +1 more source
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Chemischer Informationsdienst. Organische Chemie, 1971
AbstractDas Epoxid (I) gibt bei der Umsetzung mit Na‐azid in Äthylenglykol das Hydroxyazid (IIa) (92% Ausbeute), dessen Tosylat (IIb) durch Reaktion mit Naboranat in das Androstandiol‐Derivat (III) (90%) übergeführt wird.
KURT PONSOLD, WOLFGANG PREIBSCH
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AbstractDas Epoxid (I) gibt bei der Umsetzung mit Na‐azid in Äthylenglykol das Hydroxyazid (IIa) (92% Ausbeute), dessen Tosylat (IIb) durch Reaktion mit Naboranat in das Androstandiol‐Derivat (III) (90%) übergeführt wird.
KURT PONSOLD, WOLFGANG PREIBSCH
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Chemische Berichte, 1971
Abstract2.3β‐Imino‐5α‐androstanol‐(17β) (2a) wurde aus 2.3α‐Epoxy‐5α‐androstanon‐(17) über den entsprechenden Azidoalkoholsulfonsäureester synthetisiert und zu 3α‐Chlor‐2β‐amino‐5α‐androstanol‐(17β) (3) umgesetzt. Aus diesen beiden Verbindungen wurden Oxazoline, Thioxothiazolidine, Aminoalkohole und Aminothiole dargestellt.
Kurt Ponsold, Wolfgang Preibsch
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Abstract2.3β‐Imino‐5α‐androstanol‐(17β) (2a) wurde aus 2.3α‐Epoxy‐5α‐androstanon‐(17) über den entsprechenden Azidoalkoholsulfonsäureester synthetisiert und zu 3α‐Chlor‐2β‐amino‐5α‐androstanol‐(17β) (3) umgesetzt. Aus diesen beiden Verbindungen wurden Oxazoline, Thioxothiazolidine, Aminoalkohole und Aminothiole dargestellt.
Kurt Ponsold, Wolfgang Preibsch
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Biochimica et Biophysica Acta (BBA) - Biomembranes, 1987
We have used ESR and NMR linewidth broadening by spin-labels to determine the overall orientation of spin-labeled analogues of cholesterol and androstanol in egg lecithin bilayers. While the cholesterol analogues were found to have a single orientation in each monolayer, with the acyl chain pointing towards the center of the bilayer, the androstanol ...
G, Morrot +5 more
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We have used ESR and NMR linewidth broadening by spin-labels to determine the overall orientation of spin-labeled analogues of cholesterol and androstanol in egg lecithin bilayers. While the cholesterol analogues were found to have a single orientation in each monolayer, with the acyl chain pointing towards the center of the bilayer, the androstanol ...
G, Morrot +5 more
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Tetrahedron, 2007
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Pierre Terech, Severine Friol
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AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Pierre Terech, Severine Friol
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Journal of the Chemical Society, Perkin Transactions 1, 1973
The mass spectra of the trimethylsilyl derivatives of some androstanes containing an 11-hydroxy-substituent exhibit several prominent and characteristic ions containing the trimethylsilyl group. The mechanisms of formation of these ions have been investigated with the aid of high-resolution mass spectrometry and deuterium, 18O, and ...
P, Vouros, D J, Harvey
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The mass spectra of the trimethylsilyl derivatives of some androstanes containing an 11-hydroxy-substituent exhibit several prominent and characteristic ions containing the trimethylsilyl group. The mechanisms of formation of these ions have been investigated with the aid of high-resolution mass spectrometry and deuterium, 18O, and ...
P, Vouros, D J, Harvey
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