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Intramolecular Phosphine−Phosphine Donor−Acceptor Complexes

Inorganic Chemistry, 2009
The reaction of 5-diphenoxyphosphanyl-6-diisopropylphosphinoacenaphthene 12 with chlorotrimethylsilane unexpectedly gave a phosphonium-phosphine compound 13, containing the structural motif of four phosphorus atoms connected in a chain. To explain the mechanism of this complex transformation, a proposed intermediate 5-dichlorophosphino-6 ...
Piotr, Wawrzyniak   +3 more
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ChemInform Abstract: Phosphine—Phosphine Oxides, Phosphine—Carboxylic Acids and Phosphines Bearing Olefinic Groups

ChemInform, 2009
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
Benjamin Schaeffner, Armin Boerner
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Organoplumbyl Phosphines and Phosphine Oxides

ChemInform, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
P. J. Guiry, P. J. McCormack
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Mixed Phosphine—Phosphine Oxide Ligands

ChemInform, 2004
AbstractFor Abstract see ChemInform Abstract in Full Text.
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Dioxaphosphabicyclooctanes: small caged phosphines from tris(hydroxymethyl)phosphine

Dalton Transactions, 2023
The synthesis and coordination chemistry of sterically small caged phosphines, and their applications as ligands in homogeneous catalysis.
James D. Nobbs   +8 more
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Tertiary Amine-Mediated Reductions of Phosphine Oxides to Phosphines

Organic Letters, 2023
The reduction of phosphine oxides without the use of highly reactive reductants represents a safer and more sustainable solution for recycling of organophosphorus compounds. Herein, we disclose an N,N,N',N'-tetramethylethylenediamine (TMEDA)-mediated reduction via an unusual intermolecular hydride transfer. Mechanistic studies suggest that TMEDA serves
Keshu Yin   +4 more
openaire   +2 more sources

Enantioselective Phosphine Organocatalysis

Synlett, 2009
The broad potential synthetic usefulness of phosphine-promoted reactions has stimulated many recent investigations on enantioselective variants of known reactions of this family, as well as the search for new, specifically designed, chiral phosphorus catalysts.
Marinetti, A., Voituriez, A.
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Reduction of phosphine oxides to phosphines

Tetrahedron Letters, 2019
Abstract The digest is devoted to the most widespread reducing agents which are used for the reduction of tertiary and secondary phosphine oxides, phospholene oxides, phospholane oxides, phosphonates, phosphinates, α- and β-hydroxy and thiomethyl phosphine oxides, α-aminophosphine oxides. Stereoselectivity of reactions is described.
Evgeniya Podyacheva   +2 more
openaire   +1 more source

Phosphine-Stabilized Digermavinylidene

Journal of the American Chemical Society, 2019
An intramolecular germylene-phosphine Lewis pair (1) was reacted with germanium dichloride to give in 92% yield a phosphine adduct of a chloro substituted germyl-germylene (2). After reduction of this dichloride with strong reductants like the Mg(I) reagent {(MesNacnac)Mg}2 (72% yield) or Na (52% yield) a phosphine stabilized digermavinylidene (3) was ...
Kilian M. Krebs   +5 more
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Phosphine oxide-based tricarbonylrhenium(i) complexes from phosphine/phosphine oxide and dihydroxybenzoquinones

Dalton Transactions, 2018
Visible light absorbing PO donor-based organometallic complexes were assembled from PR3/OPR3, dihydroxybenzoquinone and Re2(CO)10.
Ramar Arumugam   +4 more
openaire   +2 more sources

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