Most syntheses in the chemical research laboratory fail and usually require several attempts before proceeding satisfactorily. Failed syntheses are not only discouraging and frustrating, but also cost a lot of time and money. Many failures may, however, be avoided by understanding the structure-reac
Side Reactions in Organic Synthesis (A Guide to Successful Synthesis Design) || The Stability of Organic Compounds
✍ Scribed by Zaragoza Dörwald, Florencio
- Publisher
- Wiley-VCH Verlag GmbH & Co. KGaA
- Year
- 2005
- Tongue
- German
- Weight
- 360 KB
- Edition
- 1
- Category
- Article
- ISBN
- 3527310215
No coin nor oath required. For personal study only.
✦ Synopsis
Most syntheses in the chemical research laboratory fail and usually require several attempts before proceeding satisfactorily. Failed syntheses are not only discouraging and frustrating, but also cost a lot of time and money. Many failures may, however, be avoided by understanding the structure-reactivity relationship of organic compounds.
This advanced textbook highlights the competing processes and limitations of the most important reactions used in organic synthesis. By allowing chemists to quickly recognize potential problems this book will help to improve their efficiency and success-rate. A must for every student but also for every chemist in industry and academia.
From The Contents:
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Organic Synthesis: General Remarks
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Stereoelectronic Effects and Reactivity
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The Stability of Organic Compounds
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Aliphatic Nucleophilic Substitutions: Problematic Electrophiles
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The Alkylation of Carbanions
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The Alkylation of Heteroatoms
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The Acylation of Heteroatoms
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Palladium-Catalyzed C-C Bond Formation
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Cyclizations
- Monofunctionalization of Symmetric Difunctional Substrates
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📜 SIMILAR VOLUMES
Scheme 9.1. Unfavorable processes according to Baldwin's rules. Scheme 9.2. Methylation of a metalated sulfone [6].
Most syntheses in the chemical research laboratory fail and usually require several attempts before proceeding satisfactorily. Failed syntheses are not only discouraging and frustrating, but also cost a lot of time and money. Many failures may, however, be avoided by understanding the structure-reac
Most syntheses in the chemical research laboratory fail and usually require several attempts before proceeding satisfactorily. Failed syntheses are not only discouraging and frustrating, but also cost a lot of time and money. Many failures may, however, be avoided by understanding the structure-reac
Most syntheses in the chemical research laboratory fail and usually require several attempts before proceeding satisfactorily. Failed syntheses are not only discouraging and frustrating, but also cost a lot of time and money. Many failures may, however, be avoided by understanding the structure-reac
Scheme 7.1. Acylations with sterically hindered carboxylic acids [5-8]. Scheme 7.12. Acylation of unprotected amino acids [42, 43]. Scheme 7.13. Regioselective acylation of a 2,6-diaminopurine [44].