Results 191 to 200 of about 7,119 (254)

Structure-reactivity based control of radical-mediated degradation in thiol-Michael hydrogels.

open access: yesJ Mater Chem B
Kirkpatrick BE   +7 more
europepmc   +1 more source
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Vinyl sulfones

Acta Crystallographica Section C Crystal Structure Communications, 2008
Four neutral vinyl sulfones, two of which are paired with phosphonate groups, are described. The compounds are diisopropyl (2-phenylethenylsulfonylmethyl)phosphonate, C(15)H(23)O(5)PS, (I), diisopropyl {[2-(7-methoxy-1,3-benzodioxol-5-yl)ethenylsulfonyl]methylsulfonylmethyl}phosphonate, C(18)H(27)O(10)PS(2), (II), bis(trans-2-phenylethenyl) sulfone, C ...
Jessica H, Wong   +3 more
openaire   +2 more sources

Synthesis of nucleoside sulfonates and sulfones

Tetrahedron Letters, 1991
Abstract Sulfonate analogues of adenine, cytidine and guanine monophosphates have been synthesized for the first time. The synthesis of ribose 3-sulfonate, a synthesis of sulfonyl disaccharides and dinucleotides and an improved synthesis of a ribose 3-sulfone is also reported.
Branislav Musicki, Theodore S. Widlanski
openaire   +1 more source

Synthesis of carbohydrate sulfonates and sulfonate esters

The Journal of Organic Chemistry, 1990
La reaction d'esters α-lithio sulfonates avec des hydrures de carbohydrates primaires est une voie simple de synthese de sulfonates-analogues de phosphates hydrocarbones importants comme le glucose 6-phosphate, le ribose 5-phosphate et l'uridine 5-phosphate.
Branislav Musicki, Theodore S. Widlanski
openaire   +1 more source

Amphiphilic perfluoroalkylated sulfones and sulfonate betaines

Journal of Fluorine Chemistry, 2007
Abstract Two types of perfluoro alkyl-containing amphiphilic sulfones 7 – 9 and 13 – 15 , respectively, and sulfonate betaines 23 – 32 were prepared using 2-[(perfluoroalkyl)methyl]oxiranes ( 1–3 , R F  = C 4 F 9 , C 6 F 13 , C 8 F 17 ) or 3-(perfluoroalkyl)propyl iodides ( 16 and 17 , R F  = C 6 F 13 , C 8 F 17 ) as the starting compounds ...
Robert Kaplánek, Oldřich Paleta
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Sulfonation and Sulfation

Industrial & Engineering Chemistry, 1951
E. E. Gilbert, E. P. Jones
openaire   +1 more source

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