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PHOSPHOLE

Phosphole

Chemical compound

Phosphole is the organic compound with the chemical formula C 4H 4PH; it is the phosphorus analog of pyrrole. The term phosphole also refers to substituted

Phosphole

Arsole

Chemical compound

derivatives have similar structure and chemical properties to those of phosphole derivatives. When arsole is fused to a benzene ring, this molecule is

Arsole

Phosphorus porphyrin

Organophosphorus compound

their core or porphyrins with one of the four pyrroles substituted for a phosphole. Unmodified porphyrins are composed of pyrroles and linked by unsaturated

Phosphorus porphyrin

Phosphorus_porphyrin

Heterocyclic compound

Molecule with one or more rings composed of different elements

Furan (Oxole not used) Silicon Silolane Silole Phosphorus Phospholane Phosphole Sulfur Thiolane Thiophene (Thiole not used) Germanium Germolane Germole

Heterocyclic compound

Heterocyclic_compound

Metallole

an oxygen analog Gallole, a gallium analog Germole, a germanium analog Phosphole, a phosphorus analog Pyrrole (azole), a nitrogen analog Selenophene, a

Metallole

Pyrrole

Organic ring compound (C4H4NH)

sheet (SDS) Chemical Safety Data Related compounds Related compounds Phosphole, arsole, bismole, stibole Except where otherwise noted, data are given

Pyrrole

Stibole

Chemical compound

Molar mass 174.844 g·mol−1 Related compounds Related compounds Pyrrole, phosphole, arsole, bismole Except where otherwise noted, data are given for materials

Stibole

Phosphorine

Chemical compound

phosphorus tribromide. Ring-opening approaches have been developed from phospholes. Structural studies by electron diffraction reveal that phosphorine is

Phosphorine

Organophosphine

Class of chemical compounds

(unsaturated: phosphirenes), five-membered rings are phospholanes (unsaturated: phosphole), and six-membered rings are phosphinanes. Tertiary (3°) phosphines, with

Organophosphine

Phosphetane

Chemical compound

formula C3H7P, is one atom larger than phosphiranes, one smaller than phospholes, and is the heavy-atom analogue of azetidines. The first known phosphetane

Phosphetane

McCormack reaction

Chemical reaction

hydrolyzed to give the phosphine oxide. Dehydrohalogenation gives the phosphole. W. B. McCormack (1973). "3-Methyl-1-Phenylphospholene oxide". Organic

McCormack reaction

McCormack_reaction

Magnetic inequivalence

1-substituted or unsubstituted pyrrole and related aromatic heterocyclics (phospholes, furan, thiophene, etc.) as well as unsubstituted or 1-substituted cyclopentadienes

Magnetic inequivalence

Magnetic_inequivalence

Benzophosphole

Chemical compound

substituted derivatives of the parent heterocycle. Organophosphorus chemistry Phosphole Indole International Union of Pure and Applied Chemistry (2014). Nomenclature

Benzophosphole

Glutathione reductase

Enzyme

Becker K (May 2005). "Mechanistic studies on a novel, highly potent gold-phosphole inhibitor of human glutathione reductase". J. Biol. Chem. 280 (21): 20628–37

Glutathione reductase

Glutathione_reductase

Bismole

Chemical compound

Molar mass 262.064 g·mol−1 Related compounds Related compounds Pyrrole, phosphole, arsole, stibole Except where otherwise noted, data are given for materials

Bismole

Phosphetene

Chemical compound

phosphetene rings can be released by ring expansion to five-membered phosphole rings, studied for the incorporation of O, S, Se, and Pt and incorporation

Phosphetene