March's Advanced Organic Chemistry: Reactions, Mechanisms, and StructureJohn Wiley & Sons, 29 ian. 2007 - 2250 pagini The Sixth Edition of a classic in organic chemistry continues its tradition of excellence Now in its sixth edition, March's Advanced Organic Chemistry remains the gold standard in organic chemistry. Throughout its six editions, students and chemists from around the world have relied on it as an essential resource for planning and executing synthetic reactions. The Sixth Edition brings the text completely current with the most recent organic reactions. In addition, the references have been updated to enable readers to find the latest primary and review literature with ease. New features include:
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Cuprins
PART 1 | 1 |
PART 2 | 417 |
Appendix A The Literature of Organic Chemistry | 1870 |
Appendix B Classification of Reactions by Type of Compounds Synthesized | 1911 |
Indexes | 1937 |
Alte ediții - Afișează-le pe toate
March's Advanced Organic Chemistry: Reactions, Mechanisms, and Structure Michael B. Smith,Jerry March Nu există previzualizare disponibilă - 2007 |
March's Advanced Organic Chemistry: Reactions, Mechanisms, and Structure Michael B. Smith,Jerry March Nu există previzualizare disponibilă - 2007 |
Termeni și expresii frecvente
Academic Press acetic acid Acta acyl alcohols aldehydes alkenes alkyl halides allylic amines Angew anion aromatic aromatic rings aryl atom attack base benzene benzylic bromide Bull carbanions carbon carboxylic cation Chem Chim chiral chloride cleaved Commun compounds conjugate converted coupling cyclopropane discussion double bond effect electrons electrophilic enantiomers energy enol epoxides esters ethers example free radicals Friedel–Crafts give Grignard reagents halogen heterocyclic hydrogen bonding intermediate iodides isomer ketones kinetic leaving group method methyl molecule nitrogen nucleophilic substitution Olah orbitals Organic Chemistry Organic Synthesis Organomet organometallic ortho pair palladium catalyst Patai Perkin Trans phenols Phys position prepared presence primary proton Pure Appl react reaction reactivity rearrangement resonance Russ salts Schleyer SN2 mechanism SN2 reactions solvent stable steric structure substrate sulfonic Synlett Synth tertiary Tetrahedron Lett treatment vinyl Wiley