March's Advanced Organic Chemistry: Reactions, Mechanisms, and StructureJohn Wiley & Sons, 29 de gen. 2007 - 2250 pàgines 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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Continguts
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 |
Altres edicions - Mostra-ho tot
March's Advanced Organic Chemistry: Reactions, Mechanisms, and Structure Michael B. Smith,Jerry March Previsualització no disponible - 2007 |
March's Advanced Organic Chemistry: Reactions, Mechanisms, and Structure Michael B. Smith,Jerry March Previsualització no disponible - 2007 |
Frases i termes més freqüents
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 Commun complex compounds conjugate converted coupling discussion double bond effect electrons electrophilic enantiomers energy enol epoxides esters ethers example free radicals give Grignard reagents H H H halogen heterocyclic hydrogen bonding intermediate iodides isomer kcal ketones kinetic leaving group mechanism method methyl molÀ1 molecule nitrogen nucleophilic substitution Olah orbitals Organic Chemistry Organomet organometallic ortho pair palladium catalyst Patai Perkin Trans phenols Phys position prepared presence proton Pure Appl react reaction reactivity rearrangement resonance Russ salts Schleyer SN2 reactions solvent stable steric structure substrate sulfonic Synlett Synth Synthesis tertiary Tetrahedron Lett tion treatment vinylic Wiley