Modern Methods of Organic SynthesisCambridge 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. |
Зміст
I | 1 |
II | 75 |
III | 105 |
V | 111 |
VI | 118 |
VII | 120 |
VIII | 123 |
IX | 125 |
XXI | 253 |
XXII | 259 |
XXIII | 268 |
XXIV | 299 |
XXV | 315 |
XXVI | 331 |
XXVII | 349 |
XXVIII | 360 |
X | 132 |
XI | 144 |
XII | 148 |
XIII | 151 |
XIV | 159 |
XVI | 211 |
XVII | 219 |
XVIII | 222 |
XIX | 231 |
XX | 238 |
XXIX | 365 |
XXX | 370 |
XXXI | 378 |
XXXII | 394 |
XXXIII | 405 |
XXXIV | 422 |
XXXV | 434 |
XXXVI | 454 |
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Modern Methods of Organic Synthesis South Asia Edition W Carruthers,Iain Coldham Обмежений попередній перегляд - 2015 |
Загальні терміни та фрази
a,ẞ-unsaturated acetate adduct aldehyde aldehydes or ketones aldol reaction alkene alkenyl alkyl alkynes allylic alcohol amine Angew anion anti aromatic asymmetric B. M. Trost borane boron carbon atom carbon-carbon carbonyl carbonyl compounds carbonyl group catalyst Chem chloride CO₂Et CO₂H CO₂Me Comprehensive Organic Synthesis conjugate addition cyclic cycloaddition cycloaddition reactions derivatives diastereomer Diels-Alder reaction diene dienophile dihydroxylation double bond electrophile elimination enantioselectivity enol ether epoxide ester example Fleming formation formed functional groups gave give Grignard reagent H₂O halides hydroboration hydrogen atom intermediate intramolecular isomer ketone less-hindered Lewis acid lithium aluminium hydride MeO2C metal method methyl mixture nucleophilic OH OH Organic Synthesis organolithium Oxford oxidation oxygen Pergamon Press Ph Ph presence proton radical react reactive readily rearrangement reduction regioselectivity ring salt selectivity SiMe3 sodium solvent species stereoselectivity substituents substrates sulfone takes place Tetrahedron Lett transition unsaturated ylide Z-alkene