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Strategies and tactics in organic synthesis. Vol. 10 /
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 secondhand analysis, we are given stories that vividly demo...
| Clasificación: | Libro Electrónico |
|---|---|
| Otros Autores: | |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Burlington :
Elsevier Science,
2014.
|
| Colección: | Strategies and Tactics in Organic Synthesis ;
v. 10. |
| Temas: | |
| Acceso en línea: | Texto completo Texto completo |
MARC
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| 082 | 0 | 4 | |a 547.2 |
| 245 | 0 | 0 | |a Strategies and tactics in organic synthesis. |n Vol. 10 / |c edited by Michael Harmata. |
| 260 | |a Burlington : |b Elsevier Science, |c 2014. | ||
| 300 | |a 1 online resource | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
| 338 | |a online resource |b cr |2 rdacarrier | ||
| 490 | 1 | |a Strategies and Tactics in Organic Synthesis ; |v v. 10 | |
| 588 | 0 | |a Print version record. | |
| 505 | 0 | |a Substrate-Directed Heck-Matsuda Arylations; ( -- )-Berkelic Acid: Lessons Learned From Our Investigations on a Scalable Total Synthesis; The Mysterious Case of the Kingianins; Total Synthesis of Chinensiolide B: An Exercise in Functional Group Selectivity with the Help of a Fortuitous Side Product and a Good Nose; Syntheses of the Bisindole Alkaloids of the Genera Borreria and Flindersia; Synthesis of (�)-Amathaspiramide F: Stereochemical Switch of a [2,3]-Stevens ; Oxabicyclic Building Blocks as Key Intermediates in the Synthesis of the Natural Products ( -- )-Platensimycin and (+)-Frondosin A; Structure Inspires a New Method That Delivers the Synthesis of Natural Products and Analogs in the Pederin Family; Gliocladin C: The Development and Application of a Pyrroloindoline-Indole Radical Coupling Reaction; Studies in the Synthesis of Biaryl Natural Products: The 6,6'-Binaphthopyranones; Sleepless Nights: The Total Synthesis of the Anticancer Australian Rainforest Polyketide EBC-23; Total Synthesis of the Crinipellins. | |
| 520 | |a 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 secondhand analysis, we are given stories that vividly demonstrate the power of the human endeavor known as organic synthesis and the creativity and tenacity of its practitioners. | ||
| 650 | 0 | |a Organic compounds |x Synthesis. | |
| 650 | 6 | |a Compos�es organiques |x Synth�ese. |0 (CaQQLa)201-0020323 | |
| 650 | 7 | |a SCIENCE |x Chemistry |x Organic. |2 bisacsh | |
| 650 | 7 | |a Organic compounds |x Synthesis |2 fast |0 (OCoLC)fst01047668 | |
| 700 | 1 | |a Harmata, Michael. | |
| 776 | 0 | 8 | |i Print version: |a Harmata, Michael. |t Strategies and Tactics in Organic Synthesis. |d Burlington : Elsevier Science, �2014 |z 9780124171855 |
| 830 | 0 | |a Strategies and Tactics in Organic Synthesis ; |v v. 10. | |
| 856 | 4 | 0 | |u https://sciencedirect.uam.elogim.com/science/book/9780124171855 |z Texto completo |
| 856 | 4 | 0 | |u https://sciencedirect.uam.elogim.com/science/bookseries/18746004/10 |z Texto completo |
| 880 | 8 | |6 505-00/(S |a 1.2. Traditional Methods for the Synthesis of α-Methylene γ-Lactones1.3. Use of 2-Alkoxycarbonyl Allylboronates to Access α-Methylene γ-Lactones; 2. Model Studies and Retrosynthetic Analysis; 2.1. Retrosynthetic Analysis; 2.2. Model Studies; 3. Design and Synthesis of the Key Allylboronate; 3.1. Selection of the Protecting Group; 3.2. Synthesis of Disubstituted Allylboronate 7; 4. Synthesis of the Cyclopentyl Aldehyde Substrate; 4.1. Literature Precedent; 4.2. Preparation of Aldehyde 6; 5. Critical Moment-The Key Aldehyde Allylboration Step | |
| 880 | 8 | |6 505-00/(S |a 7. Synthesis of Kingianin A8. ``Go Fish� � -Pursuit of the Intermolecular RCDA Approach; 9. Formal Synthesis of Kingianin A and Synthesis of Kingianins D, F, H, and J; 10. NCI 60 Test Results for Kingianins A (NSC#D-768505/1) and H (NSC#D-768506/1); 11. Reconsidering the Biosynthesis; 12. Conclusions; Acknowledgments; References; Chapter 4: Total Synthesis of Chinensiolide B: An Exercise in Functional Group Selectivity with the Help of a Fortuitous Side product and a good nose; 1. Introduction; 1.1. Chinensiolide and Other α-Methylene γ-Lactones in Nature | |