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目錄

1 Introduction
2 Functional group chemistry: the basics
2.1 Selectivity of organic reactions
2.2 Functionalization ofalkanes
2.3 Functionalization ofalkencs
2.4 Functionalization ofalkynes
2.5 Functionalization of aromatic hydrocarbons
2.6 Functionalization of substituted benzene derivatives
2.7 Functionalization of simple heterocyclic compounds
2.8 Interconversion of functional groups Summary
3 Formation of carbon-carbon bonds: the principles
3.1 General strategy
3.2 Disconnections and synthons
3.3 Electrophilic carbon species
3.4 Nucleophilic carbon species Summary
4 Formation of carbon-carbon bonds: reactions of organometallic
compounds
4.1 Grignard reagents and electrophiles
4.2 Other organometallic reagents and electrophiles
4.3 Reactions of nucleophiles derived from alk-l-ynes
4.4 Review
4.5 Worked examples Summary
5 Formation of carbon-carbon bonds: the use of stabilized carbanions
and related nucleophiles
5.1 Carbanions stabilized by two -M groups
5.2 Carbanions stabilized by one -M group
5.3 Carbanions stabilized by neighbouring phosphorus or sulfur
5.4 Nucleophilic acylation
5.5 Alkene, arene and heteroarene nucleophiles
5.6 Review
5.7 Worked examples Summary
6 Formation of carbon-heteroatom bonds: the principles
6.1 Carbon-halogen bonds
6.2 Carbon-oxygen, carbon-sulfur and carbon-selenium bonds
6.3 Carbon-nitrogen and carbon-phosphorus bonds
6.4 Carbon-silicon bonds Summary
7 Ring closure （and ring opening）
7.1 lntramolecular cyclization by electrophile-nucleophile interaction
7.2 Cycloaddition
7.3 Electrocyclic ring closure
7.4 Ring opening
7.5 Review
7.6 Worked examples Summary
8 Reduction
8.1 Catalytic hydrogenation
8.2 Metal hydride reductions
8.3 Electron-transfer reactions
8.4 Reduction of specific functional groups
8.5 Reductive cleavage of carbon-heteroatom bonds
8.6 Reductive ring opening of oxiranes
8.7 Reduction Of a/B-unsaturated carbonyl compounds
8.8 Reduction of conjugated dienes
8.9 Reduction of aromatic and heteroaromatic compounds Summary
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9 Oxidation
10 Protective groups
11 Boron reagents
12 Phosphorus reagents
13 Silicon reagents
14 Selenium reagents
15 Asymmetric synthesis
16 Selected synthese
Endnotes to the text
Further reading
Index

前言/序言

有機閤成指南（第3版） 下載 mobi epub pdf txt 電子書

評分☆☆☆☆☆

很好，很好，價格實惠

評分☆☆☆☆☆

好好學習

評分☆☆☆☆☆

使用方便。很有幫助，工具書

評分☆☆☆☆☆

很好，很好，價格實惠

評分☆☆☆☆☆

好很

評分☆☆☆☆☆

very goodvery goodvery good

評分☆☆☆☆☆

很有參考價值，溫故而知新

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閤成初學者的入門書，正好可以復習下英語，方便看文獻專利

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小冊子，字體有點小，不過我個人還能接受。裏麵的內容還是比較全的，條理也比較清楚，不過不太適閤初學者，適閤有一定有機閤成基礎的人作為提高，或者工作的人作參考書使用

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