{"product_id":"methods-and-applications-of-cycloaddition-reactions-in-organic-syntheses-9781118299883","title":"Methods and Applications of Cycloaddition","description":"\u003cb\u003eBook Synopsis\u003c\/b\u003e\u003cbr\u003eAlthough 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.\u003cbr\u003e\u003cbr\u003e\u003cb\u003eTable of Contents\u003c\/b\u003e\u003cbr\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","brand":"John Wiley \u0026 Sons Inc","offers":[{"title":"Default Title","offer_id":49406848041303,"sku":"9781118299883","price":170.95,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0817\/1739\/5799\/files\/9781118299883.jpg?v=1730497328","url":"https:\/\/bookcurl.com\/products\/methods-and-applications-of-cycloaddition-reactions-in-organic-syntheses-9781118299883","provider":"Book Curl","version":"1.0","type":"link"}