PAAL–KNORR Pyrrole Synthesis to PURDIE Sugar OH Methylation

Abstract

This article contains brief overviews, mechanisms and practical details for organic synthesis named reactions and processes beginning with the letter ‘P’. Reactions included in this section are: PAAL–KNORR Pyrrole Synthesis; PADWA Pyrroline Synthesis; PARHAM Cyclization via Lithiation of Aryl Bromides; PARNES Methyl Transfer; PASSERINI Isonitrile C O Condensation; PASTO–MATTESON α-Bromoorganoborane Rearrangement; PATERNO–BUCHI [2 + 2] Cycloaddition; PAUSON–KHAND Cyclopentenone Annulation; PAYNE Epoxide Rearrangement; von PECHMAN–DUISBERG Coumarin Synthesis; von PECHMAN Diazo-olefin Cycloaddition; PEARLMAN Pd Hydrogenolysis Catalyst; PEDERSEN Crown Ethers; PEDERSEN Niobium Coupling Reagents; PERKIN Carboxylic Acids (Esters) from Malonates; PERKIN Coumarin Rearrangement; PERKOW Vinyl Phosphate Synthesis; PETASIS 3-Component Amine Synthesis; PETASIS Titanocene Carbene Olefination; PETERSON Olefination via β-Silyl Alcohol; PFALTZ—EVANS Chiral Bis-oxazolines; PFAU – PLATTNER Cyclopropane Synthesis; PFITZINGER Quinoline Synthesis; PFITZNER–MOFFAT Alcohol Oxidation; PICTET–HUBERT Phenanthridine Synthesis; PICTET–SPENGLER Isoquinoline Synthesis; PILLOTY–ROBINSON Indole Synthesis; PINHEY Arylation; PINNER lmino Ether Synthesis; PINNICK Aldehyde Oxidation; PIRKLE Alcohol Resolution; POLONOVSKY N -Oxide Rearrangement; POMERANZ–FRITSCH–SCHLITTER Isoquinoline Synthesis; POSNER Trioxane Synthesis; PRELOG–STOLL Acyloin Condensation; PREVOST–WOODWARD Olefin Hydroxylation; PRILEJAEV Epoxidation; PRINS Alkene Hydroxyalkylation; PSCHORR Arylation via Diazonium Salts; PUDOVIK Hydroxy Phosphonate Synthesis; PUMMERER Sulfoxide Rearrangement; PURDIE Sugar OH Methylation