Name Reactions and Reagents in Organic Synthesis Bradford P. Mundy, Frank G. Favaloro, Michael G. Ellerd
Publisher: Wiley-Interscience

Silas Cook of our own IU Chemistry Department. The app has a flash-card type design. To date these reactions are of great importance At high temperatures, in the reaction mixture, migration of the acyl group from 1- to 6-position which is named as transacylation and protiodeacylation of the acyl group at the 1-position of 1-acyl-2-methoxy naphthalene are possible. This app was created by undergraduates at Indiana University under the guidance of Prof. In this monograph approximately 500 name reactions are included, of which over 200 represent newer name reactions and modern reagents. It now contains 15 name reactions which will hopefully be expanding in the future. A recent American Chemical Society award winner for creative work in organic chemistry2, Ei-ichi Negishi produced a highly efficient coupling reaction in 19773 that has varied applications in pharmaceuticals today. Highly General Stereo-, Regio-, and Chemo-Selective Synthesis of Terminal and Internal Conjugated Enynes by the Pd-Catalysed Reaction of Alkynylzinc Reagents with Alkenyl Halides. One can explore reactions by name (reaction to name, name to reaction), by mechanism, or by missing reagents or products. (a) Name Reactions and Reagents in Organic Synthesis.Mundy, B. The Friedel-Crafts reaction has a long history in organic synthesis for electrophilic aromatic substitution reactions such as alkylations and acylations.