Reconstruction of simultaneous multislice imaging magnetic resonance data (example) v1 (protocols.io.pmndk5e)

protocols.io ◽  
2018 ◽  
Author(s):  
Klaus Eickel
Keyword(s):  
Magnetic Resonance ◽  
Magnetic Resonance Data ◽  
Resonance Data ◽  
Simultaneous Multislice ◽  
Multislice Imaging

Methods to Determine Phytopharmaceuticals in Tobacco and Tobacco Products. 4th Report: A Procedure to Determine Vamidothion and its Metabolites/Methoden zur Bestimmung von Phytopharmaka in Tabak und Tabakerzeugnissen: IV. Mitteilung: Ein Bestimmungsverfahren fuer Vamidothion und seine Metaboliten

1977 ◽  
Vol 9 (2) ◽  
Author(s):  
A.N. Sagredos ◽  
R. Moser
Keyword(s):  
Mass Spectrometry ◽  
Nuclear Magnetic Resonance ◽  
Acetic Acid ◽  
Magnetic Resonance ◽  
Aluminium Oxide ◽  
Nuclear Magnetic Resonance Data ◽  
Gas Chromatograph ◽  
Tobacco Products ◽  
Magnetic Resonance Data ◽  
Resonance Data

AbstractBased on previous work (7) a method to simultaneously determine vamidothion [I], vamidothion-sulfoxide [II] and vamidothion sulfone [III] in tobacco has been developed. The compounds are extracted with water/acetone/acetic acid from the tobacco, cleansed over an aluminium oxide column and then determined on the gas chromatograph with the specific sulphur detector. Rates of recovery are 70 % - 92 %, the determination level is 0.1 ppm. Mass spectrometry and nuclear magnetic resonance data of vamidothion [I], vamidothion-sulfoxide [ II ] and vamidothion-sulfone [III] are given.

2-Epi- and 15-dihydro-2-epilubimin: new stress compounds from the potato

1980 ◽  
Vol 58 (19) ◽  
pp. 2069-2072 ◽  
Author(s):  
A. Stoessl ◽  
J. B. Stothers
Keyword(s):  
Magnetic Resonance ◽  
Pathogenic Fungus ◽  
Reduction Product ◽  
Magnetic Resonance Data ◽  
Resonance Data

The complement of sesquiterpenoidal stress compounds produced in the interaction of potato with the pathogenic fungus, Alternariasolani, includes representatives of a new stereochemical series, 2-epilubimin (1) and its reduction product, 15-dihydro-2-epilubimin (3). Their structures were deduced from 13C and 1H magnetic resonance data.

Lignans of western red cedar (Thuja plicata Donn). VI. Dihydroxythujaplicatin methyl ether

1967 ◽  
Vol 45 (3) ◽  
pp. 305-309 ◽  
Author(s):  
Harold MacLean ◽  
Koji Murakami
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Methyl Ether ◽  
Degradation Products ◽  
Parent Compound ◽  
Thuja Plicata ◽  
Red Cedar ◽  
Magnetic Resonance Data ◽  
Resonance Data ◽  
Thuja Plicata Donn

Proof of structure is presented for another lignan of the thujaplicatin series, 2,3-dihydroxy-2-(4″-hydroxy-3″,5″-dimethoxybenzyl)-3-(4′-hydroxy-3′-methoxybenzyl)-butyrolactone (I) (dihydroxythujaplicatin methyl ether). Analytical and spectral (ultraviolet, infrared, and nuclear magnetic resonance) data on derivatives and degradation products, in addition to the parent compound, are presented.

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