Buch, Englisch, Band 4, 436 Seiten, Format (B × H): 229 mm x 152 mm
Buch, Englisch, Band 4, 436 Seiten, Format (B × H): 229 mm x 152 mm
Reihe: Strategies and Tactics in Organic Synthesis
ISBN: 978-0-12-450287-1
Verlag: William Andrew Publishing
In this book we learn how synthesis is really done and are educated, challenged and inspired by these stories, which portray the idea that triumphs do not come without challenges. We also learn that we can meet challenges to further advance the science and art of organic synthesis, driving it forward to meet the demands of society, in discovering new reactions, creating new designs and building molecules with atom and step economies that provide solutions through function to create a better world.
- Personal accounts of research in organic chemistry.
- Written by internationally renowned scientists.
- Details state of the art organic synthesis.
Zielgruppe
Organic chemists; libraries at all colleges and universities and chemical and pharmaceutical companies.
Autoren/Hrsg.
Weitere Infos & Material
1. Methodology Validation and Structure Correction by Total Synthesis: the Case of the Clerodane Diterpenoid, Sacacarin.
2. Total Synthesis of (±)Cylindrospermopsin.
3. The Total Synthesis of (-)-Arisugacin A.
4. Total Synthesis of Kainoids by Dearomatizing Anionic Cyclization.
5. Total Synthesis of Jatrophatrione, an Unprecedented [5.9.5] Tricyclic Antileukemic Diterpene.
6. Alkynyliodonium Salts in Organic Synthesis.
7. How to Thread a String Through the Eye of a Molecular Needle: Template Synthesis of Interlocked Molecules.
8. Total Synthesis of Spongistatin 1 (Altohyrtin A): a Tale of Ten Aldols.
9. The Ring-Closing Metathesis Approach to Fumagillol.
10. Devising an Especially Efficient Route to the 'Miracle' Nutrient Coenzyme Q10.
11. Total Synthesis of Lipid I and Lipid II: Late Stage Intermediates Utilized in Bacterial Cell Wall Biosynthesis.
12. Ring Rearrangement Metathesis (RRM) - A New Concept in Piperidine and Pyrrolidine Synthesis.
13. Catalytic Asymmetric Total Synthesis of (-) -Strychnine and Fostriecin.
14. The Synthesis of (±)-Strychnine via a Cobalt Mediated [2 + 2 + 2] Cycloaddition.