Sphingomyelin multiple phase behavior as revealed by multinuclear magnetic resonance spectroscopy

Biochemistry ◽  
1978 ◽  
Vol 17 (26) ◽  
pp. 5745-5750 ◽  
Author(s):  
Philip L. Yeagle ◽  
William C. Hutton ◽  
R. Bruce Martin
2003 ◽  
Vol 58 (11) ◽  
pp. 1035-1040 ◽  
Author(s):  
Bernd Wrackmeyera ◽  
Sergej V. Gruener ◽  
Alla S. Zolotareva

Abstract Methoxyethynyl(trimethyl)silane (1a) reacts at 100°C very slowly with triethylborane (4) to give a mixture of alkenes, one of which is the 1,1-organoboration product (Z)-1-methoxy-1-trimethylsilyl- 2-diethylboryl-but-1-ene (7a). Methoxyethynyl(trimethyl)germane (2a) reacts within minutes at 60 - 70°C with 4, tripropylborane (5) and 9-ethyl-9-borabicyclo[3.3.1]nonane (6) by 1,1-organoboration in the usual regio- and stereospecific way to give the corresponding alkenes (9a - 11a). The analogous reactions of the ethoxyethynyl(trimethyl)germane (2b) require longer heating and are accompanied by decomposition of 2b. Ethoxyethynyl(trimethyl)stannane (3b) reacts with the trialkylboranes 4- 6 already below room temperature by 1,1-organoboration to give the alkenes (12b - 14b) in quantitative yield. The compound 3b also reacts with the alkenes, e.g. 9a, 13b, 14b, to give novel organometallicsubstituted dienes. All products were characterised by multinuclear magnetic resonance spectroscopy (1H, 11B, 13C, 29Si, and 119Sn NMR).


Stroke ◽  
2015 ◽  
Vol 46 (2) ◽  
pp. 441-446 ◽  
Author(s):  
Johann Philipp Zöllner ◽  
Elke Hattingen ◽  
Oliver C. Singer ◽  
Ulrich Pilatus

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