A new application about 1034-39-5

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In an article, published in an article, once mentioned the application of 1034-39-5, Name is Dibromotriphenylphosphorane,molecular formula is C18H15Br2P, is a conventional compound. this article was the specific content is as follows.Formula: C18H15Br2P

Efficient synthesis of benzylic bromides under neutral conditions on solid support

A method of benzylic alcohol bromination on solid phase in neutral conditions was developed. Its application to the preparation of brominated linkers is described. (C) 2000 Elsevier Science Ltd.

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Reference£º
Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate

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Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.name: Dibromotriphenylphosphorane. In my other articles, you can also check out more blogs about 1034-39-5

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 1034-39-5, Name is Dibromotriphenylphosphorane, name: Dibromotriphenylphosphorane.

Role of N-donor groups on the stability of hydrazide based hypercoordinate silicon(IV) complexes: Theoretical and experimental perceptions

A triphenylphosphinimino donor group is illustrated as a ligand in pentacoordinate siliconium halide dichelates, [YSiL2]+X-, where L is the bidentate ligand -OC(R)=NN=PPh3)- (R = t-Bu-Ph or Ph), Y = Me, Ph, CH2Cl, CHCl2, Cl or Br, and X = Cl or Br. All the new complexes were characterized by NMR spectroscopy and elemental analysis. The remote substituent, the t-Bu-phenyl or phenyl group, imparts more pentacoordinate character, i.e. more ionization to the complexes, compared to the PhCH2 group. DFT calculations indicate that the central silicon atom, due to the more positive charge, demands greater electron density. As a result of this, shorter Si-O, Si-N and Si-Cl bonds were observed. Both theoretical and experimental analysis indicate that the phosphinimino ligand is a stronger donor than the previously studied dimethylamino and isopropylidenimino ligands, causing all of the complexes to be pentacoordinate siliconium-halide salts in solution. The hypercoordinate silicon dichelates undergo unique intermolecular chelate exchange reactions: (i) complete ligand transfer from the dichelates to PhSiCl3 by a ligand priority order and (ii) bidentate ligand interchange between the dichelates and a trimethylsilyl-hydrazide precursor. Thermolysis of some selected hypercoordinated silicon(IV) complexes containing a silicon-carbon sigma-bond significantly undergo a two step decomposition, while other complexes with silicon-halogen sigma-bonds follow three steps. The thermal decomposition strongly depends on the nature of the substituents directly attached to the central silicon atom.

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Reference£º
Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate

Extracurricular laboratory:new discovery of 1034-39-5

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Synthetic Route of 1034-39-5. Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 1034-39-5, Name is Dibromotriphenylphosphorane

Activation of [99(m)TcO4]- by phosphonium cations

Phosphonium salts in solution or bound to solid phase supports interact with the robust [99(m)TcO4]- anion in neutral water. This activated form of [99(m)TcO4]- represents a source for complexes with the fac-{99mTc VIIO3}+ core, which can be synthesized in high yields and purity. This journal is the Partner Organisations 2014.

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Reference£º
Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate

Properties and Exciting Facts About Dibromotriphenylphosphorane

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 1034-39-5, 1034-39-5

1034-39-5, Name is Dibromotriphenylphosphorane, molecular formula is C18H15Br2P, belongs to chiral-phosphine-ligands compound, is a common compound. In a patnet, assignee is Gray, Nancy M.1034-39-5, once mentioned the new application about 1034-39-5

Dihetero nitrogen-containing cycloheteroethanoanthracene derivatives as antipsychotic agents

A class of ethanoanthracene derivatives is described having use in treatment of CNS disorders such as psychotic, convulsive and dystonic disorders. Compounds of particular interest are those of the formula wherein each of R5 and R6 is independently selected from hydrido, loweralkyl, benzyl and phenyl; wherein each of R7 through R?? is independently selected from hydrido, loweralkyl, hydroxy, benzyl, phenyl, loweralkoxy, phenoxy, benzyloxy, halo and haloloweralkyl; wherein R?? may be selected from hydrido, loweralkyl, cycloalkyl of five or six carbon atoms, cycloalkylalkyl of six or seven carbon atoms, phenyl, hydroxyloweralkyl, and heteroaryl selected from saturated or fully unsaturated heterocyclic rings containing five to seven ring members of which one or two ring members are nitrogen atom; wherein each Y is independently one or more groups selected from hydrido, hydroxy, loweralkyl, benzyl, phenyl, loweralkoxy, phenoxy, haloloweralkyl, halo, and loweralkanoyl; and wherein each of R?? through R?0 is independently selected from hydrido, lower alkyl, benzyl, phenyl and halo; wherein R?? together with one of R??, R?4, R?9 or R?0 may form a fused heterocyclic ring containing five or six ring members; or a pharmaceutically-acceptable salt thereof.

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Reference£º
Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate