Cargando…
Organic Synthesis : State of the Art 2007-2009.
Organic synthesis is a vibrant and rapidly evolving field; we can now cyclize amines directly onto alkenes. Like the first two books in this series, Organic Synthesis: State of the Art 2003-2005 and Organic Synthesis: State of the Art 2005-2007, this reference leads readers quickly to the most impor...
| Clasificación: | Libro Electrónico |
|---|---|
| Autor principal: | |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Oxford :
Oxford University Press, USA,
2011.
|
| Temas: | |
| Acceso en línea: | Texto completo |
MARC
| LEADER | 00000cam a2200000Mi 4500 | ||
|---|---|---|---|
| 001 | EBOOKCENTRAL_ocn747410632 | ||
| 003 | OCoLC | ||
| 005 | 20240329122006.0 | ||
| 006 | m o d | ||
| 007 | cr |n|---||||| | ||
| 008 | 110822s2011 enk o 000 0 eng d | ||
| 040 | |a EBLCP |b eng |e pn |c EBLCP |d OCLCQ |d MERUC |d ZCU |d ICG |d OCLCO |d OCLCF |d INT |d OCLCQ |d U3W |d OCLCO |d AU@ |d OCLCQ |d TKN |d OCLCQ |d DKC |d OCLCQ |d OCLCO |d OCLCQ |d OCLCO |d OCLCL | ||
| 066 | |c (S | ||
| 020 | |a 9780199842391 | ||
| 020 | |a 0199842396 | ||
| 020 | |z 9780199764549 |q (hardcover ; |q alk. paper) | ||
| 035 | |a (OCoLC)747410632 | ||
| 050 | 4 | |a QD262 .T284 2011 | |
| 082 | 0 | 4 | |a 547.2 |
| 049 | |a UAMI | ||
| 100 | 1 | |a Taber, Douglass. | |
| 245 | 1 | 0 | |a Organic Synthesis : |b State of the Art 2007-2009. |
| 260 | |a Oxford : |b Oxford University Press, USA, |c 2011. | ||
| 300 | |a 1 online resource (253 pages) | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
| 338 | |a online resource |b cr |2 rdacarrier | ||
| 520 | |a Organic synthesis is a vibrant and rapidly evolving field; we can now cyclize amines directly onto alkenes. Like the first two books in this series, Organic Synthesis: State of the Art 2003-2005 and Organic Synthesis: State of the Art 2005-2007, this reference leads readers quickly to the most important recent developments. Two years of 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 three volumes in this series. Important topics that are covered range from po | ||
| 588 | 0 | |a Print version record. | |
| 505 | 0 | |6 880-01 |a Cover; Contents; Preface; Organic Functional Group Interconversion and Protection; 1. Best Synthetic Methods: Oxidation and Reduction; 2. Functional Group Transformations; 3. Best Synthetic Methods: Oxidation; 4. Best Synthetic Methods: Reduction; 5. Best Synthetic Methods: Functional Group Transformation; 6. New Methods for Functional Group Conversion; 7. Organic Functional Group Interconversion: ( -- )-Ý-Conhydrine (Barua) and (+)-6'-Hydroxyarenarol (Anderson); 8. New Methods for Functional Group Conversion; 9. Protection of Organic Functional Groups. | |
| 505 | 8 | |a 10. Best Synthetic Methods: Functional Group Protection11. Functional Group Protection; C-H Functionalization; 12. Intermolecular and Intramolecular C-H Functionalization; 13. C-H Functionalization to Form C-O, C-N, and C-C Bonds; 14. Functionalization of C-H Bonds: The Baran Synthesis of Dihydroxyeudesmane; Carbon-Carbon Bond Construction; 15. New Methods for Carbon-Carbon Bond Construction; 16. Best Synthetic Methods: Carbon-Carbon Bond Construction; 17. C-C Single Bond Construction; 18. Construction of Alkenes, Alkynes and Allenes; Reactions of Alkenes. | |
| 505 | 8 | |a 19. Reduction, Oxidation and Homologation of Alkenes20. Reactions of Alkenes; 21. Selective Reactions of Alkenes; Alkene and Alkyne Metathesis; 22. Developments in Alkene Metathesis; 23. Developments in Alkene and Alkyne Metathesis; 24. Advances in Alkene and Alkyne Metathesis; 25. Developments in Alkene Metathesis; 26. Alkene Metathesis: Synthesis of Kainic Acid, Pladienolide B and Amphidinolide Y; 27. Alkene and Alkyne Metathesis: Phaseolinic Acid (Selvakumar), Methyl 7-Dihydro-trioxacarcinoside B (Koert), Arglabin (Reiser) and Amphidinolide V (Fürstner). | |
| 505 | 8 | |a 28. Alkene Metathesis: Synthesis of Panaxytriol (Lee), Isofagomine (Imahori and Takahata), Elatol (Stoltz), 5-F[Sub(2t)]-Isoprostane (Snapper), and Ottelione B (Clive)29. Total Synthesis by Alkene Metathesis: Amphidinolide X (Urpí/Vilarrasa), Dactylolide (Jennings), Cytotrienin A (Hayashi), Lepadin B (Charette), Blumiolide C (Altmann); Enantioselective Construction of Acyclic Stereogenic Centers; 30. Enantioselective Assembly of Oxygenated Stereogenic Centers; 31. Enantioselective Assembly of Aminated Stereogenic Centers; 32. Enantioselective Preparation of Secondary Alcohols and Amines. | |
| 505 | 8 | |a 33. Enantioselective Preparation of Alcohols and Amines34. Enantioselective Synthesis of Alcohols and Amines; 35. Enantioselective Assembly of Alkylated Stereogenic Centers; 36. Enantioselective Construction of Alkylated Stereogenic Centers; 37. Enantioselective Construction of Alkylated Centers; 38. Enantioselective Construction of Alkylated Stereogenic Centers; 39. Stereocontrolled Construction of Arrays of Stereogenic Centers; 40. Enantioselective Construction of Arrays of Stereogenic Centers; 41. Stereocontrolled Construction of Arrays of Stereogenic Centers. | |
| 590 | |a ProQuest Ebook Central |b Ebook Central Academic Complete | ||
| 650 | 0 | |a Organic compounds |x Synthesis |x Research. | |
| 650 | 4 | |a Organic compounds |x Synthesis |x Research. | |
| 650 | 4 | |a Organic compounds |x Synthesis. | |
| 650 | 4 | |a Organic compounds. | |
| 650 | 6 | |a Composés organiques |x Synthèse |x Recherche. | |
| 650 | 7 | |a Organic compounds |x Synthesis |x Research |2 fast | |
| 758 | |i has work: |a Organic synthesis (Text) |1 https://id.oclc.org/worldcat/entity/E39PCGjJKkDyyJMPhgTpDH7Jpd |4 https://id.oclc.org/worldcat/ontology/hasWork | ||
| 776 | 0 | 8 | |i Print version: |a Taber, Douglass. |t Organic Synthesis : State of the Art 2007 - 2009. |d Oxford : Oxford University Press, USA, ©2011 |z 9780199764549 |
| 856 | 4 | 0 | |u https://ebookcentral.uam.elogim.com/lib/uam-ebooks/detail.action?docID=760039 |z Texto completo |
| 880 | 0 | |6 505-00/(S |a Title Page -- Copyright Page -- Contents -- Preface -- 1. Best Synthetic Methods: Oxidation and Reduction -- 2. Functional Group Transformations -- 3. Best Synthetic Methods: Oxidation -- 4. Best Synthetic Methods: Reduction -- 5. Best Synthetic Methods: Functional Group Transformation -- 6. New Methods for Functional Group Conversion -- 7. Organic Functional Group Interconversion: ( -- )-β-Conhydrine (Barua) and (+)-6'-Hydroxyarenarol (Anderson) -- 8. New Methods for Functional Group Conversion -- 9. Protection of Organic Functional Groups -- 10. Best Synthetic Methods: Functional Group Protection -- 11. Functional Group Protection -- 12. Intermolecular and Intramolecular C-H Functionalization -- 13. C-H Functionalization to Form C-O, C-N, and C-C Bonds -- 14. Functionalization of C-H Bonds: The Baran Synthesis of Dihydroxyeudesmane -- 15. New Methods for Carbon-Carbon Bond Construction -- 16. Best Synthetic Methods: Carbon-Carbon Bond Construction -- 17. C-C Single Bond Construction -- 18. Construction of Alkenes, Alkynes and Allenes -- 19. Reduction, Oxidation and Homologation of Alkenes -- 20. Reactions of Alkenes -- 21. Selective Reactions of Alkenes -- 22. Developments in Alkene Metathesis -- 23. Developments in Alkene and Alkyne Metathesis -- 24. Advances in Alkene and Alkyne Metathesis -- 25. Developments in Alkene Metathesis -- 26. Alkene Metathesis: Synthesis of Kainic Acid, Pladienolide B and Amphidinolide Y -- 27. Alkene and Alkyne Metathesis: Phaseolinic Acid (Selvakumar), Methyl 7-Dihydro-trioxacarcinoside B (Koert), Arglabin (Reiser) and Amphidinolide V (Fürstner) -- 28. Alkene Metathesis: Synthesis of Panaxytriol (Lee), Isofagomine (Imahori and Takahata), Elatol (Stoltz), 5-F2t-Isoprostane (Snapper), and Ottelione B (Clive). | |
| 880 | 8 | |6 505-01/(S |a 49. C-O Ring Natural Products: ( -- )-Serotobenine (Fukuyama-Kan), ( -- )-Aureonitol (Cox), Salmochelin SX (Gagné), Botcinin F (Shiina), ( -- )-Saliniketal B (Paterson), Haterumalide NA (Borhan) -- 50. Complex Cyclic Ethers: (+)-Conocarpan (Hashimoto), ( -- )-Brevisamide (Satake/Tachibana), (+)-Bruguierol A (Fañanás/Rodríguez), ( -- )-Berkelic Acid (Snider), and ( -- )-Aigialomycin D (Harvey) -- 51. New Methods for Stereoselective Construction of N-Containing Rings -- 52. Stereoselective C-N Ring Construction -- 53. New Methods for C-N Ring Construction -- 54. Stereocontrolled Construction of C-N Rings: The Vanderwal Synthesis of Norfluorocurarine -- 55. Alkaloid Synthesis: Paliurine F, Lepadiformine, and 7-Deoxypancratistatin -- 56. Adventures in Alkaloid Synthesis: (+)-α-Kainic Acid (Jung), 223AB (Ma), Pumiliotoxin 251F (Jamison), Spirotryprostatin B (Trost), ( -- )-Drupacine (Stoltz) -- 57. Stereocontrolled Alkaloid Construction: Rhazinicine (Gaunt), 9-epi-Pentazocine (Zhai and Li), Fawcettidine (Dake), Strychnine (Padwa), and Yohimbine (Jacobsen) -- 58. Alkaloid Synthesis: ( -- )-Aurantioclavine (Stoltz), ( -- )-Esermethole (Nakao/Hiyama/Ogoshi), ( -- )-Kainic Acid (Tomooka), Dasycarpidone (Bennasar), ( -- )-Cephalotaxine (Ishibashi) and Lysergic Acid (Fujii/Ohno) -- 59. Alkaloid Synthesis: Crispine A (Zhou), Cermizine C (Zhang), Tangutorine (Poupon), FR901483 (Kerr), Serratezomine A (Johnston) -- 60. Synthesis of Substituted Benzenes: The Carter Synthesis of Siamenol -- 61. Preparation of Benzene Derivatives -- 62. Preparation of Benzene Derivatives: The Barrett Syntheses of Dehydroaltenuene B and 15G256β -- 63. Substituted Benzenes: The Alvarez-Manzaneda Synthesis of ( -- )-Taiwaniquinone G -- 64. Synthesis of Heteroaromatics -- 65. Preparation of Heteroaromatic Derivatives -- 66. Preparation of Heteroaromatics -- 67. Heterocycle Construction: The Chang Synthesis of Louisianin C. | |
| 938 | |a ProQuest Ebook Central |b EBLB |n EBL760039 | ||
| 994 | |a 92 |b IZTAP | ||