LEADER 05575nam 2200709 450 001 9910797481303321 005 20230807221129.0 010 $a1-118-72657-X 010 $a1-118-72655-3 035 $a(CKB)3710000000449147 035 $a(EBL)2055786 035 $a(SSID)ssj0001517179 035 $a(PQKBManifestationID)12589714 035 $a(PQKBTitleCode)TC0001517179 035 $a(PQKBWorkID)11500324 035 $a(PQKB)10416820 035 $a(PQKBManifestationID)16226117 035 $a(PQKB)24142192 035 $a(MiAaPQ)EBC2055786 035 $a(MiAaPQ)EBC4180266 035 $a(DLC) 2015021541 035 $a(Au-PeEL)EBL4180266 035 $a(CaPaEBR)ebr11296241 035 $a(CaONFJC)MIL814363 035 $a(OCoLC)910475659 035 $a(EXLCZ)993710000000449147 100 $a20161118h20152015 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 00$aHandbook of reagents for organic synthesis $ereagents for heteroarene functionalization /$fedited by Andre? B. Charette 210 1$aWest Sussex, England :$cWiley,$d2015. 210 4$dİ2015 215 $a1 online resource (829 p.) 225 1 $aHdbk of Reagents for Organic Synthesis 300 $aIncludes indexes. 311 $a1-118-72659-6 327 $aHandbook of Reagents for Organic Synthesis: Reagents for Heteroarene Functionalization; Contents; Preface; Introduction; Recent Review Articles and Monographs; Short Note on InChIs and InChIKeys; Acetic Anhydride; Acetyl Chloride; Aluminum Chloride; Aluminum Trifluoromethanesulfonate; Antimony Trifluoromethanesulfonate; Bathophenanthroline; 1,2-Benzodiazine; Benzopyrazole; Benzotriazole; Bis(allyl)di-?-chlorodipalladium; Bis(benzonitrile)dichloropalladium(II); Bis(dibenzylideneacetone)palladium(0); Bis(1,10-phenanthroline)palladium Hexafluorophosphate 327 $aBis[tris(1,1-dimethylethyl)-phosphine]palladiumBromine; N-Bromosuccinimide; n-Butyllithium; sec-Butyllithium; tert-Butyllithium; Butyllithium-Potassium tert-Butoxide; Cesium Acetate; N-Chlorosuccinimide; Copper(II) Acetate; Copper(II) Bromide; Copper(I) Chloride; Copper(II) Chloride; Copper(I) Iodide; Copper(II) Trifluoroacetate; Copper(II) Trifluoromethanesulfonate; N-Cyano-4-methyl-N-phenylbenzenesulfonamide; Dibenzofuran; Dibenzothiophene; 1,1-Di-tert-butyl Peroxide; Di-tert-butyl(methyl)phosphine; Di-tert-butyl(methyl)phosphonium Tetrafluoroborate; Dichlorobis(acetonitrile) Palladium 327 $aDichlorobis(triphenylphosphine)-palladium(II)Di-?-chlorotetrakis[(1,2-?)-cyclooctene]diiridium; Di-?-methoxobis(1,5-cyclooctadiene)diiridium(I); Dimethyl Diazomalonate; (2S,5S)-2-(1,1-Dimethylethyl)-3-methyl-5-(phenylmethyl)-4-imidazolidinone; Diphenyliodonium Hexafluorophosphate; Diphenyliodonium Triflate; Dysprosium Trifluoromethanesulfonate; N-fluoro-N-(phenylsulfonyl)-benzenesulfonamide; 1-Fluoro-2,4,6-trimethylpyridinium Tetrafluoroborate; Furan; Gallium(III) Trifluoromethanesulfonate (Gallium Triflate); Hafnium(IV) Trifluoromethanesulfonate; Hypofluorous Acid-Acetonitrile Complex 327 $aIndium(III) TriflateIndolizine; Iron, Bis(pyridine)bis(2-pyridinecarboxylato-N1,O2); Isoindole; Isoquinoline; Lithium t-Butoxide; Lithium Dichloro(1-methylethyl)-magnesate; Lithium Dichloro(2,2,6,6-tetramethylpiperidinato)-zincate; Magnesium tert-butoxide; Manganese(III) Acetate; 4-Methoxypyridine N-oxide; 6-Methoxyquinoline-N-oxide; 2-Methylbenzothiazole; N-Methylimidazole; N-Methylindole; 1-[[(4-Methylphenyl)sulfonyl]amino]-pyridinium inner salt; Methyltrioxorhenium; Nitric Acid; 4,4,4,?4,?5,5,5,?5-?Octamethyl-2,2-?bi-1,3,2-dioxaborolane; 1,2,5-Oxadiazole; Oxalyl Chloride-Dimethylformamide 327 $aOxazolePalladium(II) Acetate; Palladium(II) Bromide; Palladium(II) Chloride; Palladium(?-cinnamyl) Chloride Dimer; Palladium Pivalate; Pentamethylcyclopentadienylrhodium(III) chloride dimer; 1,10-Phenanthroline; 1,10-Phenanthroline, 1-Oxide; (1,10-Phenanthroline)(trifluoromethyl) (triphenylphosphine)copper; Pinacolborane; Pivalic Acid; Potassium Acetate; Propanoic acid, 2-Diazo-, 2-Methyl-1-(1-methylethyl)propyl ester; Pyridazine; Pyridazine N-Oxide; Pyridine; Pyridine N-Oxide; Pyrrole; Quinoline; Ruthenium Dodecacarbonyltri Triangulo; Scandium Trifluoromethanesulfonate; Silver(I) Acetate 327 $aSilver(I) Carbonate 330 $a Heteroarenes are among the most prevalent structural units in natural products, pharmaceuticals, agrochemicals, and other compounds of scientific or commercial interest. In the last decade, a broad range of novel synthetic methods has been developed to not only facilitate construction of the heteroarene motif, but to enable its modification through direct C?H functionalization. This Handbook describes 117 key reagents for selective heteroarene functionalization reactions, including both traditional and transition metal-catalyzed C?H functionalization. Since these reactions typically involve o 410 0$aHdbk of Reagents for Organic Synthesis 606 $aOrganic compounds$xSynthesis 606 $aHeterocyclic chemistry 606 $aChemical tests and reagents 615 0$aOrganic compounds$xSynthesis. 615 0$aHeterocyclic chemistry. 615 0$aChemical tests and reagents. 676 $a547/.2 702 $aCharette$b Andre? B. 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910797481303321 996 $aHandbook of reagents for organic synthesis$984290 997 $aUNINA