Modern Methods of Organic Synthesis
Cambridge University Press, 14 жовт. 2004 р. - 493 стор.
The fourth edition of this well-known textbook discusses the key methods used in organic synthesis, showing the value and scope of these methods and how they are used in the synthesis of complex molecules. All the text from the third edition has been revised, to produce a modern account of traditional methods and an up-to-date description of recent advancements in synthetic chemistry since the previous edition. A new chapter on the functionalisation of alkenes has been included and greater emphasis on highly stereoselective reactions and radical chemistry has been placed. Reference style has been improved to include footnotes on each page, allowing easy and rapid access to the primary literature. The book will be of significant interest to chemistry and biochemistry students at advanced undergraduate and graduate level, as well as researchers in academia and industry who wish to familiarise themselves with modern synthetic methods.
Відгуки відвідувачів - Написати рецензію
Не знайдено жодних рецензій.
Інші видання - Показати все
a,ß-unsaturated acetate acid active addition addition reactions adduct agent alcohol aldehyde aldol alkene alkenyl alkyl alkynes allows allylic allylic alcohol alternative amine Angew anion asymmetric atom B. M. Trost base carbon carbon-carbon carbonyl carbonyl compounds carbonyl group catalyst Chem chiral chloride CO2Et CO2Me complex compounds conjugate converted corresponding cyclic deprotonation derivatives Diels-Alder reaction diene dienophile double bond effective elimination enolate epoxidation ester ether example Fleming followed formation formed functional gave give halides heat hydride hydrogen intermediate intramolecular involves ketone leads ligand lithium metal method methyl mixture normally obtained occurs OH OH Oxford oxidation Pergamon Press Ph Ph possible prepared presence promote provides radical reactive readily reagents rearrangement reduction ring salt Scheme selectivity sodium solution species stable stereoisomer stereoselectivity substituents substrate takes place temperature Tetrahedron trans transition unsaturated yield ylide