Strategies and tactics in organic synthesis. Vol. 6 /
A classic in the area of organic synthesis, Strategies and Tactics in Organic Synthesis provides a forum for investigators to discuss their approach to the science and art of organic synthesis. Rather than a simple presentation of data or a second-hand analysis, we are given stories that vividly dem...
Clasificación: | Libro Electrónico |
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Otros Autores: | |
Formato: | Electrónico eBook |
Idioma: | Inglés |
Publicado: |
Amsterdam ; San Diego, CA ; Oxford :
Elsevier,
2005.
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Edición: | 1st ed. |
Temas: | |
Acceso en línea: | Texto completo Texto completo |
Tabla de Contenidos:
- Chapter 1. The Total Synthesis Of
- Luzopeptins.
- Chapter 2. Synthesis of Geldanamycin
- Using Glycolate Aldol Reactions.
- Chapter 3. From Methylene Bridged Glycoluril
- Dimers To Cucurbit[N]Uril Analogs With Some Detours Along The Way.
- Chapter 4. Application Of Silicon-Assisted
- Intramolecular Cross-Coupling In
- Total Synthesis Of (+)-Brasilenyne.
- Chapter 5. Samarium(II) Promoted Ketyl Olefin
- Cyclizations Applied To The Total
- Syntheses Of (
- )-Steganone And
- (+)-Isoschizandrin.
- Chapter 6. The Synthesis Of Polycavernoside A.
- An Example Of Conformationally Guided
- Macrolactonization.
- Chapter 7. First Total Synthesis Of Several Natural
- Products Based On Alkyne-Co<INF>2</INF>(Co)<INF>6</INF> Complexes.
- Chapter 8. Total Synthesis Of Myriaporones 1, 3, and 4.
- Chapter 9. Adventures In Natural Product Synthesis:
- From Deep Sea Sponge To Pilot Plant. The Large Scale Total Synthesis Of The Marine
- Natural Product (+)-Discodermolide.
- Chapter 10. Synthesis Of Aprepitant.
- Chapter 11. Total Synthesis And Mechanism Of Action Studies On The Antitumor Alkaloid, (
- )-Agelastatin A.
- Chapter 12. Design And Synthesis of Cooperative "Pinwheel" Fluorescent Sensors.
- Chapter 13. Functionalization Of Pyridines And
- Thiazoles Via The Halogen-Dance Reaction,
- Application To The Total Synthesis Of
- Caerulomycin C And WS75624 B.
- Chapter 14. Diastereoselective Intramolecular
- 4+3 Cycloaddition And An Enantioselective
- Total Synthesis Of (+)-Dactylol.