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P-Chiral phosphine

Index P-Chiral phosphine

P-Chiral phosphines are organophosphorus compounds of the formula PRR'R", where R, R', R". [1]

12 relations: Amine, Asymmetric hydrogenation, BINAP, C2-Symmetric ligands, DIPAMP, Enantioselective synthesis, Homogeneous catalysis, Ligand, Organocatalysis, Organophosphorus compound, Pyramidal inversion, Racemization.

Amine

In organic chemistry, amines are compounds and functional groups that contain a basic nitrogen atom with a lone pair.

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Asymmetric hydrogenation

Asymmetric hydrogenation is a chemical reaction that adds two atoms of hydrogen preferentially to one of two faces of an unsaturated substrate molecule, such as an alkene or ketone.

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BINAP

BINAP (2,2'-bis(diphenylphosphino)-1,1'-binaphthyl) is an organophosphorus compound.

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C2-Symmetric ligands

In homogeneous catalysis, a C2-symmetric ligands usually describes bidentate ligands that are dyssymmetric but not asymmetric by virtue of their C2-symmetry.

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DIPAMP

DIPAMP is an organophosphorus compound that is used as a ligand in homogeneous catalysis.

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Enantioselective synthesis

Enantioselective synthesis, also called asymmetric synthesis, is a form of chemical synthesis.

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Homogeneous catalysis

In chemistry, homogeneous catalysis is catalysis in a solution by a soluble catalyst.

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Ligand

In coordination chemistry, a ligand is an ion or molecule (functional group) that binds to a central metal atom to form a coordination complex.

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Organocatalysis

In organic chemistry, the term organocatalysis (a portmanteau of the terms "organic" and "catalyst") refers to a form of catalysis, whereby the rate of a chemical reaction is increased by an organic catalyst referred to as an "organocatalyst" consisting of carbon, hydrogen, sulfur and other nonmetal elements found in organic compounds.

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Organophosphorus compound

Organophosphorus compounds are organic compounds containing phosphorus.

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Pyramidal inversion

In chemistry, pyramidal inversion is a fluxional process in compounds with a pyramidal molecule, such as ammonia (NH3) "turns inside out".

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Racemization

In chemistry, racemization is the conversion of an enantiomerically pure mixture (one where only one enantiomer is present) into a mixture where more than one of the enantiomers are present.

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Redirects here:

Chiral phosphine, Kwon phosphine, Phosphine inversion.

References

[1] https://en.wikipedia.org/wiki/P-Chiral_phosphine

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