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Pyrrhotites from reactors

Pyrroie is a very weak acid.

Pyrroiizidine alkaloid-derived pheromones identified from the hairpencils

Pyrrole 2-carboxylate.

Pyrrole and imidazole are five-membered, nitrogen-containing heterocycles but have six -n electron arrangements, much like that of the cyclopentadienyl anion. Both have a lone pair of electrons on nitrogen in a p orbital perpendicular to the ring.

Pyrrole and imidazole are five-membered, nitrogen-containing heterocycles but have six it electron arrangements like that of the cyclopentadienyl anion. Both have a lone pair of electrons on nitrogen map orbital perpendicular to the ring.

Pyrrole and imidazole are five-membered, nitrogen-containing heterocycles but have six tt electron arrangements, much like that of the cyclopentadienyl anion. Both have a lone pair of electrons on nitrogen in a p orbital perpendicular to the ring.

Pyrrole and indole based anion receptors 1-3.

Pyrrole and indole intermolecular C-H C-X coupling

Pyrrole and thiophene-based receptors containing separate redox-active reporter groups.

Pyrrole and thiophene-based redox-active receptors.

Pyrrole borylation in the synthesis of rhazinicine by Gaunt

Pyrrole containing awsa-ferrocenes.

Pyrrole derivatives

Pyrrole derivatives from phenyl isocyanide and 2-isocyanopyridine.

Pyrrole dithiocarbamate in which the thioureide resonance is inaccessible.

Pyrrole esters .

Pyrrole formation217

Pyrrole is an electron-rich ring.

Pyrrole is aromatic but not basic. It does not have any unshared electron pairs. The electron pair on nitrogen is part of the aromatic system.

Pyrrole molecule, Clouds above and below plane of ring total of six n electrons, the aromatic sextet.

Pyrrole or 3,4-ethylenedioxythiophene CD complex formation in water and oxidative polymerization of CD complexes

Pyrrole reacts with strong bases such as sodamide.

Pyrrole thiourea derivatives evaluated for catalytic activity and selectivity in the asymmetric acetyl-Pictet-Spengler reaction.

Pyrrole- 2-Carboxyamide—crystal structure motif containing centrosymmetric dimers with double N-H- O H-bonds.



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