{"product_id":"methods-and-applications-of-cycloaddition-reactions-in-organic-syntheses-isbn-9781118299883","title":"Methods and Applications of Cycloaddition Reactions in Organic Syntheses","description":"\u003cp\u003e\u003cb\u003eAdvanced tools for developing new functional materials and applications in chemical research, pharmaceuticals, and materials science\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eCycloadditions are among the most useful tools for organic chemists, enabling them to build carbocyclic and heterocyclic structures. These structures can then be used to develop a broad range of functional materials, including pharmaceuticals, agrochemicals, dyes, and optics. With contributions from an international team of leading experts and pioneers in cycloaddition chemistry, this book brings together and reviews recent advances, trends, and emerging research in the field.\u003c\/p\u003e \u003cp\u003e\u003ci\u003eMethods and Applications of Cycloaddition Reactions in Organic Syntheses\u003c\/i\u003e focuses on two component cycloadditions, with chapters covering such topics as:\u003c\/p\u003e \u003cul\u003e \u003cli\u003eN1 unit transfer reaction to C–C double bonds\u003c\/li\u003e \u003cli\u003e[3+2] Cycloaddition of \u003ci\u003eα, β\u003c\/i\u003e-unsaturated metal-carbene complexes\u003c\/li\u003e \u003cli\u003eFormal [3+3] cycloaddition approach to natural product synthesis\u003c\/li\u003e \u003cli\u003eDevelopment of new methods for the construction of heterocycles based on cycloaddition reaction of 1,3-dipoles\u003c\/li\u003e \u003cli\u003eCycloreversion approach for preparation of large \u003ci\u003eπ\u003c\/i\u003e-conjugated compounds\u003c\/li\u003e \u003cli\u003eTransition metal-catalyzed or mediated [5+1] cycloadditions\u003c\/li\u003e \u003c\/ul\u003e \u003cp\u003eReaders will learn methods for seamlessly executing important reactions such as Diels-Alder and stereoselective dipolar reactions in order to fabricate heterocyclic compounds, natural products, and functional molecules. The book not only features cutting-edge topics, but also important background information, such as the contributors’ process for developing new methodologies, to help novices become fully adept in the field. References at the end of each chapter lead to original research papers and reviews for facilitating further investigation of individual topics.\u003c\/p\u003e \u003cp\u003eCovering the state of the science and technology, \u003ci\u003eMethods and Applications of Cycloaddition Reactions in Organic Syntheses\u003c\/i\u003e enables synthetic organic chemists to advance their research and develop new functional materials and applications in chemical research, pharmaceuticals, and materials science.\u003c\/p\u003e  \u003cp\u003e\u003ci\u003ePREFACE ix\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003ci\u003eCONTRIBUTORS xi\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003ePART I [2+1] CYCLOADDITION\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e1 [2+1]-TYPE CYCLOPROPANATION REACTIONS 1\u003cbr\u003e \u003ci\u003eAkio Kamimura\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e2 N1 UNIT TRANSFER REACTION TO C__C DOUBLE BONDS 67\u003cbr\u003e \u003ci\u003eSatoshi Minakata, Youhei Takeda, and Kensuke Kiyokawa\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003ePART II [2+2] CYCLOADDITION\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e3 LEWIS BASE CATALYZED ASYMMETRIC FORMAL [2þ2] CYCLOADDITIONS 89\u003cbr\u003e \u003ci\u003eAndrew D. Smith, James Douglas, Louis C. Morrill, and Edward Richmond\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003ePART III [2+2] AND [4+2]\/[2+2] CYCLOADDITION\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e4 CATALYTIC [2þ2] CYCLOADDITION OF SILYL ENOL ETHERS 115\u003cbr\u003e \u003ci\u003eYosuke Yamaoka and Kiyosei Takasu\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003ePART IV [3+2] CYCLOADDITION\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e5 [3þ2] CYCLOADDITION OF a,b-UNSATURATED METAL–CARBENE COMPLEXES 135\u003cbr\u003e \u003ci\u003eRyukichi Takagi and Manabu Abe\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e6 GEOMETRY-CONTROLLED CYCLOADDITION OF C-ALKOXYCARBONYL NITRONES: SYNTHETIC STUDIES ON NONPROTEINOGENIC AMINO ACIDS 151\u003cbr\u003e \u003ci\u003eOsamu Tamura\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e7 RECENT ADVANCES IN CATALYTIC ASYMMETRIC 1,3-DIPOLAR CYCLOADDITIONS OF AZOMETHINE IMINES, NITRILE OXIDES, DIAZOALKANES, AND CARBONYL YLIDES 175\u003cbr\u003e \u003ci\u003eHiroyuki Suga and Kennosuke Itoh\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e8 CONDENSATION OF PRIMARY NITRO COMPOUNDS TO ISOXAZOLE DERIVATIVES: STOICHIOMETRIC TO CATALYTIC 205\u003cbr\u003e \u003ci\u003eFrancesco De Sarlo and Fabrizio Machetti\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e9 CARBAMOYLNITRILE OXIDE AND INVERSE ELECTRON-DEMAND 1,3-DIPOLAR CYCLOADDITION 223\u003cbr\u003e \u003ci\u003eNagatoshi Nishiwaki and Haruyasu Asahara\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003ePART V [3+2], [3+3], AND [4+2] CYCLOADDITION\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e10 CYCLOADDITION REACTIONS OF SMALL RINGS 241\u003cbr\u003e \u003ci\u003eSteven D. R. Christie and Hayley T. A. Watson\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003ePART VI [3+2] AND [5+1] CYCLOADDITION\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e11 DEVELOPMENT OF NEW METHODS FOR THE CONSTRUCTION OF HETEROCYCLES BASED ON CYCLOADDITION REACTION OF 1,3-DIPOLES 263\u003cbr\u003e \u003ci\u003eYutaka Ukaji and Takahiro Soeta\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003ePART VII [3+3] CYCLOADDITION\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e12 A FORMAL [3þ3] CYCLOADDITION APPROACH TO NATURAL PRODUCT SYNTHESIS 283\u003cbr\u003e \u003ci\u003eJun Deng, Xiao-Na Wang, and Richard P. Hsung\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003ePART VIII [4+2] CYCLOADDITION\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e13 [4þ2] CYCLOADDITION CHEMISTRY OF SUBSTITUTED FURANS 355\u003cbr\u003e \u003ci\u003eScott Bur and Albert Padwa\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e14 SYNTHESIS OF SUBSTITUTED OLIGOACENES VIA DIELS–ALDER REACTIONS AND SUBSTITUENT EFFECTS ON MOLECULAR STRUCTURE, PACKING ARRANGEMENT, AND SOLID-STATE OPTICAL PROPERTIES 407\u003cbr\u003e \u003ci\u003eChitoshi Kitamura\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e15 CYCLOREVERSION APPROACH FOR PREPARATION OF LARGE p-CONJUGATED COMPOUNDS 429\u003cbr\u003e \u003ci\u003eHidemitsu Uno\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003ePART IX [4+2]\/[3+2] CYCLOADDITION\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e16 TANDEM [4þ2]\/[3þ2] CYCLOADDITIONS 471\u003cbr\u003e \u003ci\u003eRamil Y. Baiazitov and Scott E. Denmark\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003ePART X [5+1] CYCLOADDITION\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e17 TRANSITION METAL-CATALYZED OR -MEDIATED [5þ1] CYCLOADDITIONS 551\u003cbr\u003e \u003ci\u003eXu-Fei Fu and Zhi-Xiang Yu\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003ePART XI [4+3] CYCLOADDITION\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e18 [4þ3] CYCLOADDITIONS OF ENOLSILANE DERIVATIVES 565\u003cbr\u003e \u003ci\u003eSarah Y. Y. Lam and Pauline Chiu\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e19 APPLICATION OF THE [4þ3] CYCLOADDITION REACTION TO THE SYNTHESIS OF NATURAL PRODUCTS 599\u003cbr\u003e \u003ci\u003eDarin E. Jones and Michael Harmata\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003cb\u003ePART XII [5+2] CYCLOADDITION\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003e20 RECENT DEVELOPMENTS IN THE [5þ2] CYCLOADDITION 631\u003cbr\u003e \u003ci\u003eHervé Clavier and Hélène Pellissier\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e\u003ci\u003eINDEX 655\u003c\/i\u003e\u003c\/p\u003e  \u003cp\u003e\u003cb\u003eNAGATOSHI NISHIWAKI, PhD,\u003c\/b\u003e is Professor of Chemistry at Kochi University of Technology, Japan. Dr. Nishiwaki has published over ninety scientific papers, twenty reviews and book chapters, and ten papers in chemical education. In addition, he has presented his research results at many scientific conferences.\u003c\/p\u003e \u003cp\u003e\u003cb\u003eAdvanced tools for developing new functional materials and applications in chemical research, pharmaceuticals, and materials science\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eCycloadditions are among the most useful tools for organic chemists, enabling them to build carbocyclic and heterocyclic structures. These structures can then be used to develop a broad range of functional materials, including pharmaceuticals, agrochemicals, dyes, and optics. With contributions from an international team of leading experts and pioneers in cycloaddition chemistry, this book brings together and reviews recent advances, trends, and emerging research in the field.\u003c\/p\u003e \u003cp\u003e\u003ci\u003eMethods and Applications of Cycloaddition Reactions in Organic Syntheses\u003c\/i\u003e focuses on two component cycloadditions, with chapters covering such topics as:\u003c\/p\u003e \u003cul\u003e \u003cli\u003eN1 unit transfer reaction to C–C double bonds\u003c\/li\u003e \u003cli\u003e[3+2] Cycloaddition of \u003ci\u003eα, β\u003c\/i\u003e-unsaturated metal-carbene complexes\u003c\/li\u003e \u003cli\u003eFormal [3+3] cycloaddition approach to natural product synthesis\u003c\/li\u003e \u003cli\u003eDevelopment of new methods for the construction of heterocycles based on cycloaddition reaction of 1,3-dipoles\u003c\/li\u003e \u003cli\u003eCycloreversion approach for preparation of large \u003ci\u003eπ\u003c\/i\u003e-conjugated compounds\u003c\/li\u003e \u003cli\u003eTransition metal-catalyzed or mediated [5+1] cycloadditions\u003c\/li\u003e \u003c\/ul\u003e \u003cp\u003eReaders will learn methods for seamlessly executing important reactions such as Diels-Alder and stereoselective dipolar reactions in order to fabricate heterocyclic compounds, natural products, and functional molecules. The book not only features cutting-edge topics, but also important background information, such as the contributors’ process for developing new methodologies, to help novices become fully adept in the field. References at the end of each chapter lead to original research papers and reviews for facilitating further investigation of individual topics.\u003c\/p\u003e \u003cp\u003eCovering the state of the science and technology, \u003ci\u003eMethods and Applications of Cycloaddition Reactions in Organic Syntheses\u003c\/i\u003e enables synthetic organic chemists to advance their research and develop new functional materials and applications in chemical research, pharmaceuticals, and materials science.\u003c\/p\u003e","brand":"Wiley","offers":[{"title":"Default Title","offer_id":47989614903525,"sku":"NP9781118299883","price":231.95,"currency_code":"USD","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1842\/7735\/files\/9781118299883.jpg?v=1761784818","url":"https:\/\/k12savings.com\/products\/methods-and-applications-of-cycloaddition-reactions-in-organic-syntheses-isbn-9781118299883","provider":"K12savings","version":"1.0","type":"link"}