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Organic synthesis : state of the art 2009-2011 /
Organic synthesis is a vibrant and rapidly evolving field; we can now cyclize amines directly onto alkenes. Like its predecessors, this reference leads readers quickly to the field's more important recent developments. Two years of Douglass F. Taber's popular weekly online column, "&q...
| Clasificación: | Libro Electrónico |
|---|---|
| Autor principal: | |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Oxford :
Oxford University Press,
[2013]
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| Temas: | |
| Acceso en línea: | Texto completo |
MARC
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| 100 | 1 | |a Taber, D. F. |q (Douglass F.), |d 1948- |e author. | |
| 245 | 1 | 0 | |a Organic synthesis : |b state of the art 2009-2011 / |c Douglass F. Taber. |
| 264 | 1 | |a Oxford : |b Oxford University Press, |c [2013] | |
| 300 | |a 1 online resource (xi, 250 pages) : |b illustrations | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
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| 500 | |a "This volume is made up of the Organic highlights, published online each week (http://www.organic-chemistry.org) in 2010 and 2011, arranged by topic"--Preface. | ||
| 504 | |a Includes bibliographical references and indexes. | ||
| 588 | 0 | |a Print version record. | |
| 505 | 0 | |a Cover; Contents; Preface; Organic Functional Group Interconversion and Protection; 1. Best Synthetic Methods: Functional Group Transformations; 2. Functional Group Transformation: The Castle Synthesis of Celogentin C; 3. Organic Functional Group Conversion; 4. Advances in Organic Functional Group Transformation; 5. Organic Functional Group Transformation; 6. Best Synthetic Methods: Reduction; 7. Best Synthetic Methods: Oxidation; 8. Best Synthetic Methods: Oxidation and Reduction; 9. Oxidation and Reduction; 10. Organic Functional Group Protection. | |
| 505 | 8 | |a 11. Functional Group Protection: The Kraus Synthesis of Bauhinoxepin J12. Functional Group Protection; 13. Organic Functional Group Protection; 14. Organic Functional Group Protection and Deprotection; Flow Methods; 15. Flow Methods for Organic Synthesis; C-H Functionalization; 16. C-H Functionalization: The White Synthesis of 6-Deoxyerythronolide B; 17. C-H Functionalization: The Chen Synthesis of Celogentin C; 18. Functionalization and Homologation of C-H Bonds; Carbon-Carbon Bond Construction; 19. New Methods for Carbon-Carbon Bond Construction. | |
| 505 | 8 | |a 20. Best Synthetic Methods: C-C Bond Construction21. New Methods for C-C Bond Construction; 22. New Methods for C-C Bond Construction: The Burke Synthesis of ( -- )-Peridinin; 23. Carbon-Carbon Bond Formation; Reactions of Alkenes; 24. Best Synthetic Methods: Reactions of Alkenes; 25. Alkene Reactions: The Dabdoub/Baroni Synthesis of ()-Dihydroactinidiolide; 26. Reactions of Alkenes; 27. Functionalization and Homologation of Alkenes; Alkene and Alkyne Metathesis; 28. Advances in Alkene Metathesis: The Hoveyda Synthesis of (+)-Quebrachamine. | |
| 505 | 8 | |a 29. Alkene and Alkyne Metathesis: Navenone B (Cossy), (+)-Asperpentyn (Daesung Lee), ( -- )-Amphidinolide K (Eun Lee), Norhalichondrin B (Phillips)30. Progress in Alkene and Alkyne Metathesis: (+)-5-epi-Citreoviral (Funk) and ()-Poitediol (Vanderwal); 31. Alkene and Alkyne Metathesis: Grandisol (Goess), 8-Epihalosilane (Kouklovsky/Vincent), (+)-Chinensiolide B (Hall); 32. Alkene and Alkyne Metathesis: (+)-Anamarine (Sabitha), ()-Pseudotabersonine (Martin), Lactimidomycin (Fürstner); Enantioselective Construction of Acyclic Stereogenic Centers. | |
| 505 | 8 | |a 33. Enantioselective Preparation of Alcohols and Amines: The Suh Synthesis of ( -- )-Macrosphelide J34. Enantioselective Preparation of Alcohols and Amines; 35. Construction of Oxygenated and Aminated Stereogenic Centers; 36. Enantioselective Preparation of Alcohols and Amines: The Lam Synthesis of (+)-Tanikolide; 37. Enantioselective Construction of Alkylated Centers: The Maier Synthesis of Platencin; 38. Enantioselective Construction of Alkylated Stereogenic Centers; 39. Construction of Alkylated Stereogenic Centers; 40. Enantioselective Preparation of Alkylated Stereogenic Centers. | |
| 520 | |a Organic synthesis is a vibrant and rapidly evolving field; we can now cyclize amines directly onto alkenes. Like its predecessors, this reference leads readers quickly to the field's more important recent developments. Two years of Douglass F. Taber's popular weekly online column, ""Organic Chemistry Highlights"", as featured on the organic-chemistry.org website, are consolidated here, with cumulative indices of all four volumes in this series. Important topics that are covered range from powerful new methods for C-C bond construction to asymmetric organocatalysis and direct C-H functionalizat. | ||
| 546 | |a English. | ||
| 590 | |a eBooks on EBSCOhost |b EBSCO eBook Subscription Academic Collection - Worldwide | ||
| 650 | 0 | |a Organic compounds |x Synthesis |x Research. | |
| 650 | 0 | |a Carbon compounds |x Research. | |
| 650 | 6 | |a Composés organiques |x Synthèse |x Recherche. | |
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| 650 | 7 | |a SCIENCE |x Chemistry |x Organic. |2 bisacsh | |
| 650 | 7 | |a Organic compounds |x Synthesis |x Research |2 fast | |
| 730 | 0 | |i Based on (expression): |a Organic chemistry highlights. |x 1660-7155 | |
| 776 | 0 | 8 | |i Print version: |a Taber, D.F. (Douglass F.), 1948- |t Organic synthesis. |d Oxford : Oxford University Press, [2013] |z 9780199965724 |w (DLC) 2012540925 |w (OCoLC)819519283 |
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