LEADER 03943nam 2200601 a 450 001 9910830062003321 005 20230721025936.0 010 $a1-280-93539-1 010 $a9786610935390 010 $a0-470-17651-2 010 $a0-470-17650-4 035 $a(CKB)1000000000354922 035 $a(EBL)309776 035 $a(OCoLC)250720136 035 $a(SSID)ssj0000207811 035 $a(PQKBManifestationID)11199011 035 $a(PQKBTitleCode)TC0000207811 035 $a(PQKBWorkID)10254510 035 $a(PQKB)10437462 035 $a(MiAaPQ)EBC309776 035 $a(EXLCZ)991000000000354922 100 $a20070309d2007 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 00$aName reactions for functional group transformations$b[electronic resource] /$fedited by Jie Jack Li, E.J. Corey 210 $aHoboken, N.J. $cWiley-Interscience$dc2007 215 $a1 online resource (769 p.) 225 1 $aComprehensive Name Reactions ;$vv.1 300 $aDescription based upon print version of record. 311 $a0-471-74868-4 320 $aIncludes bibliographical references and index. 327 $aAsymmetric synthesis. CBS reduction ; Davis chiral oxaziridine reagents ; Midland reduction ; Noyori catalytic asymmetric hydrogenation ; Sharpless asymmetric hydroxylation reactions -- Reduction. Eschweiler-Clark reductive alkylation of amines ; Gribble reduction of diaryl ketones ; Luche reduction ; Meerwein-Ponndorf-Verley reduction ; Staudinger reaction ; Wharton reaction -- Oxidation. Baeyer-Villiger oxidation ; Brown hydroboration reaction ; Burgess dehydrating reagent ; Corey-Kim oxidation ; Dess-Martin periodinane oxidation ; Tamao-Kumada-Fleming oxidation ; Martin's sulfurane dehydrating reagent ; Oppenauer oxidation ; Prilezhaev reaction ; Rubottom oxidation ; Swern oxidation ; Wacker-Tsuji oxidation ; Woodward cis-dihydroxylation -- 327 $aOlefination. Chugaev elimination ; Cope elimination reaction ; Corey-Winter olefin synthesis ; Perkin reaction (cinnamic acid synthesis) ; Perkow vinyl phosphate synthesis ; Ramberg-Ba?cklund olefin synthesis ; Shapiro reaction ; Zaitsev elimination -- Amine synthesis. Fukuyama amine synthesis ; Gabriel synthesis ; Leuckart-Wallach reaction -- Carboxylic acid derivatives synthesis. Fischer-Speier esterification ; Mukaiyama esterification ; Ritter reaction ; Strecker amino acid synthesis ; Yamada coupling reagent ; Yamaguchi esterification -- Miscellaneous functional group manipulations. Balz-Schiemann reaction ; Buchwald-Hartwig reactions ; Haloform reaction ; Hunsdiecker reaction ; Japp-Klingemann hydrazone synthesis ; Krapcho decarboxylation ; Nef reaction ; Prins reaction ; Regitz diazo synthesis ; Sommelet reaction. 330 $aThis practical, well-organized reference delves deeply into functional group transformations, to provide all the detailed information that researchers need. Topics are organized into the following sections: oxidation, reduction, asymmetric synthesis, and functional group manipulations Each section includes a description of the functional group transformation, the historical perspective, mechanisms, variations and improvements on the reaction, synthetic utilities and applications for the reaction, experimental details, and references to the primary literature Contributors are 410 0$aComprehensive Name Reactions 606 $aOrganic compounds$xSynthesis 606 $aChemical reactions 615 0$aOrganic compounds$xSynthesis. 615 0$aChemical reactions. 676 $a547 676 $a547/.2 701 $aLi$b Jie Jack$0440094 701 $aCorey$b E. J$020674 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910830062003321 996 $aName reactions for functional group transformations$94116993 997 $aUNINA