From Biosynthesis to Total Synthesis
| Autor: | Alexandros L. Zografos |
|---|---|
| EAN: | 9781118753637 |
| eBook Format: | ePUB |
| Sprache: | Englisch |
| Produktart: | eBook |
| Veröffentlichungsdatum: | 22.03.2016 |
| Untertitel: | Strategies and Tactics for Natural Products |
| Kategorie: | |
| Schlagworte: | Biosynthesis biosynthetic mechanisms biosynthetic pathways biosynthetic routes chemical transformations natural products synthesis organic synthesis total synthesis |
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Focusing on biosynthesis, this book provides readers with approaches and methodologies for modern organic synthesis. By discussing major biosynthetic pathways and their chemical reactions, transformations, and natural products applications; it links biosynthetic mechanisms and more efficient total synthesis.
• Describes four major biosynthetic pathways (acetate, mevalonate, shikimic acid, and mixed pathways and alkaloids) and their related mechanisms
• Covers reactions, tactics, and strategies for chemical transformations, linking biosynthetic processes and total synthesis
• Includes strategies for optimal synthetic plans and introduces a modern molecular approach to natural product synthesis and applications
• Acts as a key reference for industry and academic readers looking to advance knowledge in classical total synthesis, organic synthesis, and future directions in the field
Alexandros L. Zografos graduated as a chemist from National University of Athens, Greece. After earning his PhD in 2001 at National Technical University of Athens he pursued postdoctoral studies with Prof. Phil Baran at The Scripps Research Institute and Prof. Scott Snyder at Columbia University before he moved back to Greece to work as a senior researcher at National University of Athens and NCRS Demokritos Institute. In 2009 he began his independent career at Aristotle University of Thessaloniki where he is currently Assistant Professor of Organic Chemistry. His group is working on divergent total synthesis of complex natural products and in the development of novel CH-activations.
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