- Fluorous tagging compounds and methods of use thereof
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A method of increasing the fluorous nature of a compound includes the step of reacting the compound with at least one second compound having the formula: wherein Rf is a fluorous group and m is 0, 1 or 2.
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- Morpholinyl silanes and use for control of plant diseases caused by fungi
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Aryl substituted morpholinyl silanes, their preparation, compositions containing said compounds and their use as agricultural fungicides are disclosed.
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- REDISTRIBUTION OF PRIMARY SILYL- AND GERMYLPHOSPHINES: SYNTHESIS OF TRISILYL- AND TRIGERMYLPHOSPHINES
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Redistribution reactions of SiH3PH2, Si2H5PH2, SiH3PH2/Si2H5PH2, and GeH3PH2 promoted by BX3(X=F, Cl, Br), B2H6, and B5H9 as routes to the trisilyl- and trigermylphosphines (SiH3)3P, (Si2H5)3P, (SiH3)2PSi2H5, and (GeH3)3P have been examined.Reaction of the silyl- or germylphosphine borane complex (e.g.SiH3PH2*BF3) with the uncomplexed silyl- or germylphosphine (e.g.SiH3PH2) appears essential to the redistribution process.Trisilylphosphines and (GeH3)3P are best obtained in RPH2(R=SiH3, Si2H5) - BF3 and GeH3PH2 - B5H9 reaction systems, respectively.
- Wingeleth, Dale E.,Norman, Arlan D.
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p. 123 - 130
(2007/10/02)
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- Arachidonic acid analogs
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Analogs of arachidonic acid are provided having the structure STR1 wherein R is CH2 OH or CO2 H and m is 1 or 2. These compounds are useful as inhibitors of leukotriene and prostaglandin biosynthesis and as such are useful an antiall
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