Methods and applications of cycloaddition reactions in organic syntheses

Although these reactions have been studied for a long time, cycloaddition chemistry makes frequent and considerable advances that requires chemists to keep constantly up–to–date with the practices and state–of–the–art. Bringing together the contributions from leading worldwide researchers, Methods and Applications of Cycloaddition Reactions in Organic Syntheses provides a valuable guidebook for synthetic organic chemists involved in chemical research, pharmaceuticals, and materials science to keep organic chemists updated and current in the practices of cycloadditions, a leading class of synthetic reaction. INDICE: Part 1. [2+1] Cycloaddition Chapter 1. [2+1]–type cyclopropanation reactions Akio Kamimura Chapter 2. N1 Unit Transfer Reaction to C–C Double Bonds Satoshi Minakata, Youhei Takada, and Kensuke Kiyokawa Part 2. [2+2] Cycloaddition Chapter 3. Lewis Base Catalysed Asymmetric Formal [2+2] Cycloadditions Andrew Smith, James Douglas, Louis Morrill, and Edward Richmond Part 3. [2+2] and [4+2]/[2+2] Cycloaddition Chapter 4. Catalytic [2+2] Cycloaddition of Silyl Enol Ethers Yosuke Yamaoka and Kiyosei Takasu Part 4. [3+2] Cycloaddition Chapter 5. [3+2] Cycloaddition of α,β–Unsaturated Metal–Carbene Complexes Ryukichi Takagi and Manabu Abe   Chapter 6. Geometry–Controlled Cycloaddition of C–Alkoxycarbonyl Nitrones: Synthetic Studies on Non–Proteinogenic Amino Acids Osamu Tamura Chapter 7. Recent Advances in Catalytic Asymmetric 1,3–Dipolar Cycloadditions of Azomethine Imines, Nitrile Oxides, Diazoalkanes, and Carbonyl Ylides Hiroyuki Suga and Kennosuke Itoh Chapter 8. Condensation of Primary Nitro Compounds to Isoxazole Derivatives: Stoichiometric to Catalytic Francesco De Sarlo and Fabrizio Machetti   Chapter 9. Carbamoylnitrile Oxide and Inverse Electron–Demand 1,3–Dipolar Cycloaddition Nagatoshi Nishiwaki and Haruyasu Asahara Part 5. [3+2], [3+3] and [4+2] Cycloaddition Chapter 10. Cycloaddition Reactions of Small Rings Steven D. R. Christie and Hayley T. A. Watson Part 6. [3+2] and [5+1] Cycloaddition Chapter 11. Development of New Methods for the Construction of Heterocycles Based on Cycloaddition Reaction of 1,3–Dipoles Yutaka Ukaji and Takahiro Soeda Part 7. [3+3] Cycloaddition Chapter 12. A Formal [3+3] Cycloaddition Approach to Natural Product Synthesis Jun Deng, Xiao–Na Wang, and Richard P. Hsung Part 8. [4+2] Cycloaddition Chapter 13. [4+2]–Cycloaddition Chemistry of Substituted Furans Scott Bur and Albert Padwa Chapter 14. Synthesis of Substituted Oligoacenes via Diels?Alder Reactions and Substituent Effects on Molecular Structure, Packing Arrangement, and Solid–state Optical Properties Chitoshi Kitamura Chapter 15. Cycloreversion Approach for Preparation of Large π–Conjugated Compounds Hidemitsu Uno Part 9. [4+2]/[3+2] Cycloaddition Chapter 16. Tandem [4+2]/[3+2] cycloadditions Ramil Y. Baiazitov and Scott E. Denmark Part 10. [5+1] Cycloaddition Chapter 17. Transition Metal–Catalyzed or Mediated [5+1] Cycloadditions Xu–Fei Fu and Zhi–Xiang Yu Part 11. [4+3] Cycloaddition Chapter 18. [4+3] Cycloadditions of Enolsilane Derivatives Sarah Y. Y. Lam and Pauline Chiu Chapter 19. Application of the [4+3]–Cycloaddition Reaction to the Synthesis of Natural Products Darin E. Jones and Michael Harmata Part 12. [5+2] Cycloaddition Chapter 20. Recent Developments in the [5+2] Cycloaddition Hervé Clavier and Hélène Pellissier

• ISBN: 978-1-118-29988-3
• Editorial: Wiley–Blackwell
• Encuadernacion: Rústica
• Páginas: 672
• Fecha Publicación: 14/02/2014
• Nº Volúmenes: 1
• Idioma: Inglés