About the Book
Please note that the content of this book primarily consists of articles available from Wikipedia or other free sources online. Pages: 26. Chapters: Indole forming reactions, Quinoline forming reactions, Paal-Knorr synthesis, Nitrone-olefin 3+2 cycloaddition, Pictet-Spengler reaction, Chichibabin pyridine synthesis, Knorr pyrrole synthesis, Bucherer-Bergs reaction, Bischler-Napieralski reaction, Bartoli indole synthesis, Povarov reaction, Leimgruber-Batcho indole synthesis, Doebner-Miller reaction, Erlenmeyer-Plochl azlactone and amino acid synthesis, Fischer indole synthesis, Hantzsch pyridine synthesis, Friedlander synthesis, Skraup reaction, Pfitzinger reaction, Lectka enantioselective beta-lactam synthesis, Gassman indole synthesis, Feist-Benary synthesis, Knorr quinoline synthesis, Bischler-Mohlau indole synthesis, Fukuyama indole synthesis, Algar-Flynn-Oyamada reaction, Gewald reaction, Aza Diels-Alder reaction, Herz reaction, Lehmstedt-Tanasescu reaction, Einhorn-Brunner reaction, Camps quinoline synthesis, Diazoalkane 1,3-dipolar cycloaddition, Banert cascade, Allan-Robinson reaction, Niementowski quinoline synthesis, Reissert indole synthesis, Auwers synthesis, Stolle synthesis, Conrad-Limpach synthesis, Madelung synthesis, Wohl-Aue reaction, Hemetsberger indole synthesis, Gould-Jacobs reaction, Bamberger triazine synthesis, Barton Zard Synthesis, Martinet dioxindole synthesis, Gabriel-Colman rearrangement, Nenitzescu indole synthesis, Hantzsch pyrrole synthesis, Robinson-Gabriel synthesis, Combes quinoline synthesis, Bernthsen acridine synthesis, Niementowski quinazoline synthesis, Larock indole synthesis, Bucherer carbazole synthesis, Fischer oxazole synthesis, Urech hydantoin synthesis, Doebner reaction, Cook-Heilbron thiazole synthesis, Pellizzari reaction. Excerpt: The Paal-Knorr Synthesis in organic chemistry is a reaction that generates either furans, pyrroles, or thiophenes from 1,4-diketones. It is a synthetically valuable method for obtaining ...
