有機閤成的現代方法 第4版 下載 mobi epub pdf 電子書 2024

基本信息

書名：有機閤成的現代方法 第4版

定價：99.00元

作者：(英)卡如薩

齣版社：世界圖書齣版公司

齣版日期：2008-10-01

ISBN：9787506292702

字數：

頁碼：

版次：1

裝幀：平裝

開本：16開

商品重量：0.822kg

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作者簡介：BILL CARRUTHERS was born in Glasgow. He won a bursary to Glasgow Uni-
versity, where he graduated with a first-class honours degree in 1946 and a Ph.D.
in 1949. He moved to Exeter in 1956, working first for the Medical Research
Council and then, from 1968, as a lecturer then senior lecturer at the Department
of Chemistry in the University of Exeter. He died in April 1990, just a few months
before he was due to retire.

內容提要

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 plex molecules. All the text from the third edition has
been revised, to produce a modem account of traditional methods and an up-to-date
de*ion of recent advancements in synthetic chemistry. The textbook maintains
a traditional and logical approach in detailing carbon--carbon bond formations,
followed by a new chapter on the functionalization of alkenes and concluding with
oxidation and reduction reactions. Reference style has been improved to include
footnotes, allowing easy and rapid access to the primary literature. In addition, a
selection of problems has been added at the end of each chapter, with answers
at the end of the book. The book will be of significant interest to chemistry and
biochemistry students at advanced undergraduate and graduate level, as well as
to researchers in academia and industry who wish to familiarize themselves with
modem synthetic methods.

目錄

Preface to the first edition
Preface to the fourth edition
1 Formation of carbon-carbon single bonds
1.1 Main-group chemistry
1.1.1 Alkylation of enolates and enamines
1.1.2 Conjugate addition reactions of enolates and enamines
1.1.3 The aldol reaction
1.1.4 Asymmetric methodology with enolates and enamines
1.1.5 Organolithium reagents
1.1.6 Organomagnesium reagents
1.1.7 Organozinc reagents
1.1.8 Allylic organometallics of boron, silicon and tin
1.2 Transition-metal chemistry
Problems
1.2.1 Organocopper reagents
1.2.2 Organochromium chemistry
1.2.3 Organocobalt chemistry
1.2.4 Organopalladium chemistry
2 Formation of carbon-carbon double bonds
2.1 B-Elimination reactions
2.2 Pyrolytic syn eliminations
2.3 Fragmentation reactions
2.4 Alkenes from hydrazones
2.5 Alkenes from 1,2-diols
2.6 Alkenes from alkynes
2.7 The Wittig and related reactions
2.8 Alkenes from sulfones
2.9 Alkenes using titanium or chromium reagents
2.10 Alkene metathesis reactions
Problems
3 Pericyclic reactions
3.1 The Diels-Alder cycloaddition reaction
3.1.1 The dienophile
3.1.2 The diene
3.1.3 Regiochemistry of the Diels-Alder reaction
3.1.4 Stereochemistry of the Diels-Alder reaction
3.1.5 Intramolecular Diels-Alder reactions
3.1.6 The retro Diels-Alder reaction
3.1.7 Asymmetric Diels-Alder reactions
3.2 Cycloaddition reactions
3.3 Cycloaddition reactions with allyl cations and allyl anions
3.4 1,3-Dipolar cycloaddition reactions
3.5 The ene reaction
3.6 -Sigmatropic rearrangements
3.6.1 The Cope rearrangement
3.6.2 The Claisen rearrangement
3.7 -Sigmatropic rearrangements
3.8 Electrocyclic reactions
Problems
4 Radical and carbene chemistry
4.1 Radicals
4.1.1 Radical abstraction reactions
4.1.2 Radical addition reactions
4.2 Carbenes
Problems
5 Functionalization of alkenes
5.1 Hydroboration
5.1.1 Reactions of organoboranes
5.2 Epoxidation and aziridination
5.2.1 Epoxidation
5.2.2 Asymmetric epoxidation
5.2.3 Aziridination
……
6 Oxidation
7 Reduction
Answers to problems
Index

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