Paper
Synthesis of 1,2-diacyloxypropyl-3-(1′,2′-diacyl-sn-glycero)-phosphonate
Published 1985 · M. C. Moschidis
Chemistry and Physics of Lipids
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12
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0
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Abstract
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Study Snapshot
The study presents a total synthesis of 1,2-diacyloxypropyl-3-(1′,2′-diacyl-sn-glycero)phosphonate, using 1,2-dipalmitoyloxypropyl phosphonic acid and 1,2-dipalmitoy
PopulationOlder adults (50-71 years)
Sample size24
MethodsObservational
OutcomesBody Mass Index projections
ResultsSocial networks mitigate obesity in older groups.
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Citations
From Symmetric Glycerol Derivatives to Dissymmetric Chlorohydrins
The study demonstrates the synthesis of dissymmetric chlorohydrin esters from symmetric 1,3-dichloro-2-propyl esters using 1,4-dioxane and sodium carbonate, with the highest yield achieved using this solvent and base combination.
2011·7citations·Carmen E. Solarte et al.·Molecules
Molecules
O-Silylated C3-halohydrins as a novel class of protected building blocks for total, regio- and stereocontrolled synthesis of glycerolipid frameworks.
O-silylated C3-halohydrins offer a flexible, regio- and stereospecific method for the total synthesis of glycerolipid constructs, offering flexible access to key intermediates.
2010·9citations·S. D. Stamatov et al.·Organic & biomolecular chemistry
Organic & biomolecular chemistry
Regioselective and Stereospecific Halosilylating Cleavage of the Oxirane System of Glycidol Derivatives as an Efficient Strategy to C2‐O‐Functionalized C3‐Vicinal Halohydrins
Regioselective and stereospecific halosilylating of glycidyl esters and ethers with trimethylsilyl halides leads to efficient production of C2-O-functionalized C3-Vicinal Halohydrins in high yields.
2008·13citations·S. D. Stamatov et al.·European Journal of Organic Chemistry
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Regioselective and stereospecific opening of an oxirane system mediated by trifluoroacetic acid and halide anions. A new direct approach to C3-vicinal halohydrins
Trifluoroacetic acid and halide anions effectively produce C3-vicinal haloalkanols in quantitative yields from glycidol derivatives with ester, ether, or silyl functionality.
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Regioselective and stereospecific cleavage of a terminal oxirane system: a novel synthetic approach to lipid mediator congeners--1,2(2,3)-diacyl-3(1)-halo-sn-glycerols.
This novel synthetic approach allows for the rapid and efficient synthesis of 1,2(2,3)-diacyl-3(1)-halo-sn-glycerols, which are important lipid mediator congeners.
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Efficient, highly regioselective, and stereospecific conversion of glycidol systems into C2-O-acylated vicinal halohydrins
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Synthesis of a phosphono analogue of cardiolipin and study of its silicic acid column chromatographic behaviour.
The phosphono analogue of cardiolipin, 1,2-dipalmitoyloxypropyl-3-(2′-hydroxy propyl-3′- (1′′,2′′-dipalmitoyl glycerol)) biphosphonate, was synthesized and studied for its
1988·2citations·M. C. Moschidis·Chemistry and physics of lipids
Chemistry and physics of lipids
Synthesis of bis(diacyloxypropyl) phosphinate
Bis(diacyloxypropyl) phosphinate can be synthesized by heating 1,2-dipalmitoyloxypropyl phosphonic acid dimethyl ester with 1,2-diacylglycerol bromohydrin at 175°C for 72 hours, followed by
1986·2citations·M. C. Moschidis·Chemistry and Physics of Lipids
Chemistry and Physics of Lipids