Results 241 to 250 of about 19,048 (288)
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Inorganic Chemistry, 2013
A one-pot, multicomponent, coordination-driven self-assembly approach was used to synthesize the first examples of neutral bridging phosphine oxide donor-based supramolecular coordination complexes. The complexes were self-assembled from a fac-Re(CO)3 acceptor, an anionic bridging O donor, and a neutral soft phosphine or hard phosphine oxide donor.
Bhaskaran, Shankar +5 more
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A one-pot, multicomponent, coordination-driven self-assembly approach was used to synthesize the first examples of neutral bridging phosphine oxide donor-based supramolecular coordination complexes. The complexes were self-assembled from a fac-Re(CO)3 acceptor, an anionic bridging O donor, and a neutral soft phosphine or hard phosphine oxide donor.
Bhaskaran, Shankar +5 more
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Highly Chemoselective Metal-Free Reduction of Phosphine Oxides to Phosphines
Journal of the American Chemical Society, 2012Unprecedented chemoselective reductions of phosphine oxides to phosphines proceed smoothly in the presence of catalytic amounts of specific Brønsted acids. By utilizing inexpensive silanes, e.g., PMHS or (EtO)(2)MeSiH, other reducible functional groups such as ketones, aldehydes, olefins, nitriles, and esters are well-tolerated under optimized ...
Yuehui, Li +5 more
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P-Arylation: Arynes to Aryl-Phosphonates, -Phosphinates, and -Phosphine Oxides
Organic Letters, 2013Synthesis of organo-phosphorus compounds and their application in organic synthesis and life sciences has been a topic of contemporary interest. Michaelis-Arbuzov reaction is the most extensively utilized method for their preparation, which works well only with aliphatic halides.
Ranjeet A, Dhokale, Santosh B, Mhaske
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Oxidation of Phosphines by Supercritical Nitrous Oxide
Organic Letters, 1999Despite its reputation for lack of reactivity at moderate temperatures, nitrous oxide is capable of oxidizing at least one class of organic compounds, the phosphines, at temperatures at or below 100 °C. The use of supercritical N2O as both the solvent and the reactant simplifies the isolation of the products and allows one to avoid the use of flammable
Scott Poh +3 more
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Phosphorylation of Furfural by Secondary Phosphine Oxides.
ChemInform, 2004AbstractFor Abstract see ChemInform Abstract in Full Text.
N. I. Ivanova +5 more
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New Dimethyl(Methylenoxyaryl)Phosphine Oxides
Phosphorus, Sulfur, and Silicon and the Related Elements, 1990Abstract From dimethyl-chloromethyl-phosphine oxides and sodium phenolates of the corresponding mono-, di-and triphenols are prepared by the Williamson reaction new dimethyl(methyleneoxyaryl)phosphine oxides containing one, two or three phosphoryl groups.
S. Varbanov, T. Tosheva, G. Borisov
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Selective reduction of allenyl(diphenyl)phosphine oxides to allyl(diphenyl)phosphine oxides
Russian Journal of Organic Chemistry, 2017The reduction of allenyl(diphenyl)phosphine oxides with HSiCl3 or LiAlH4 selectively afforded the corresponding allyl(diphenyl)phosphine oxides. 3-Methylbut-2-en-1-yl(diphenyl)phosphine oxide reacted with AlCl3 to give a mixture of 4,4-dimethyl-1-phenyl-1,2,3,4-tetrahydro-λ5-phosphinoline 1-oxide and 4,4-dimethyl-1-phenyl-1,4-dihydro-λ5-phosphinoline 1-
S. V. Lozovskiy +2 more
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New trigonal tris(phosphine oxides)
Russian Chemical Bulletin, 2004AbstractFor Abstract see ChemInform Abstract in Full Text.
S. A. Pisareva +4 more
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Preparation of functionalized phosphine oxides and phosphine sulfides
2014(±)-tert-Butylphenylphosphinothioic acid was resolved into (Rp)-(+) tert-butylphenylphosphinothioic acids 129 according to a standard procedure. The (±)- and (Rp)-phosphinothioic acids were converted into (±)- and (Rp)-tert-butylphenylthionophosphinochloridates 139 respectively by treatment with either thionyl chloride or oxalyl chloride in ...
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On The Interactions Of Allylic Phosphines And Phosphine Oxides With n-Butyllithium
2023The thesis explores the reactivity of allylic diphenyl phosphines and phosphine oxides with the basic reagent n-butyllithium. The lithiated intermediates were explored and characterised to understand their structure. They were then reacted with aldehydes and ketones to explore the utility of such reactions.
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