LEADER 04960nam 2200757Ia 450 001 9910815201303321 005 20200520144314.0 010 $a9786613400932 010 $a9781283400930 010 $a1283400936 010 $a9781118140338 010 $a1118140338 010 $a9781118140345 010 $a1118140346 010 $a9781118140314 010 $a1118140311 035 $a(CKB)2670000000133596 035 $a(EBL)818463 035 $a(OCoLC)769342419 035 $a(SSID)ssj0000581060 035 $a(PQKBManifestationID)11343473 035 $a(PQKBTitleCode)TC0000581060 035 $a(PQKBWorkID)10539990 035 $a(PQKB)10956190 035 $a(MiAaPQ)EBC818463 035 $a(Au-PeEL)EBL818463 035 $a(CaPaEBR)ebr10523257 035 $a(CaONFJC)MIL340093 035 $a(PPN)16198360X 035 $a(Perlego)1013067 035 $a(EXLCZ)992670000000133596 100 $a20110510d2012 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 00$aRadiochemical synthesis$hVolume I$iRadiopharmaceuticals for positron emission tomography /$fedited by Peter J.H. Scott, Brian G. Hockley 205 $a1st ed. 210 $aHoboken, N.J. $cWiley$d2012 215 $a1 online resource (371 p.) 225 1 $aWiley Series on Radiochemical Syntheses ;$vv.1 300 $aDescription based upon print version of record. 311 08$a9780470588956 311 08$a0470588950 320 $aIncludes bibliographical references and index. 327 $aRadiochemical Syntheses; CONTENTS; Contributors; Foreword; Preface; Abbreviations; PART I FLUORINE-18 LABELED RADIOPHARMACEUTICALS; 1. Synthesis of [18F]-Fluorodeoxyglucose ([18F]FDG); 2. Synthesis of Sodium [18F]Fluoride (Na[18F]F); 3. Radiosynthesis of 3'-Deoxy-3''-[18F]Fluorothymidine ([18F]FLT); 4. Synthesis of [18F]Fluoroazomycin Arabinoside ([18F]FAZA); 5. Synthesis of [18F]Fluoromisonidazole (1-(2-Hydroxy-3-[18F]Fluoropropyl)-2-Nitroimidazole, [18F]FMISO); 6. Synthesis of [18F]FPPRGD2; 7. Synthesis of [18F]Fluorocholine ([18F]FCH) 327 $a8. Clinical Manufacturing of [18F]-16-a-Fluoroestradiol ([18F]FES)9. Synthesis of N-Succinimidyl 4-[18F]Fluorobenzoate ([18F]SFB); 10. Synthesis of 4-(2'-Methoxyphenyl)-1-[2'-(N-2'Pyridinyl)-p-[18F]Fluorobenzamido]Ethylpiperazine [18F]MPPF; 11. Synthesis of [18F]-Fallypride; 12. Synthesis of [18F]Fluoroethyltyrosine (18F-FET); 13. Synthesis of [18F]Flumazenil ([18F]FZ); 14. Synthesis of 6-[18F]Fluorodopamine (6-[18F]FDA); 15. Synthesis of 2-([18F]Fluoro)-3-[(2S)-2-Azetidinylmethoxy]Pyridine ([18F]2FA); 16. Synthesis of [18F]-Substance-P Antagonist-Receptor Quantifier ([18F]SPA-RQ) 327 $aPART II CARBON-11 LABELED RADIOPHARMACEUTICALS17. Synthesis of [11C]Choline Chloride ([11C]CHL); 18. Synthesis of 2-(4-N-[11C]Methylaminophenyl)-6-Hydroxybenzothiazole ([11C]6-OH-BTA-1; [11C]PIB); 19. Synthesis of [11C]-meta-Hydroxyephedrine ([11C]MHED); 20. Synthesis of l-[methyl-11C]Methionine ([11C]MET); 21. Synthesis of (+)-a-[11C]Dihydrotetrabenazine ([11C]DTBZ); 22. Synthesis of [11C]Flumazenil([11C]FMZ); 23. Synthesis of [11C]Hexadecanoic Acid ([11C]Palmitic Acid); 24. Synthesis of O-methyl-11C]Metomidate ([11C]-MTO); 25. Synthesis of [11C]Carfentanil ([11C]CFN) 327 $a26. Synthesis of [carbonyl-11C]Way-10063527. Synthesis of [11C]Raclopride; 28. Synthesis of 3-Amino-4-[2-(N-Methyl-N-[11C]Methyl-Amino-Methyl)Phenylsulfanyl]-Benzonitrile ([11C]Dasb); 29. Synthesis of [11C]Acetate; 30. Synthesis of N-(2-[11C]Methoxybenzyl)-N-(4-Phenoxypyridin-3-yl)Acetamide ([11C]PBR28); PART III OTHER RADIOPHARMACEUTICALS; 31. Synthesis of [13N]Ammonia ([13N]NH3); 32. Synthesis of [68Ga]Gallium Dota-(Tyr3)-Octreotide Acetate ([68Ga]-Dotatoc); Appendix 1 Supplier Information; Index 330 $aThe ultimate reference guide to the synthesis of radiopharmaceuticals The Radiochemical Syntheses series provides scientists and professionals with a comprehensive reference to proven synthetic methods for radiochemical reactions, along with step-by-step guidance on how to replicate these syntheses in the laboratory. Volume 1 in the series focuses on the synthesis and purification of radiopharmaceuticals in clinical use today. It brings together in one complete, self-contained volume a collection of monographs containing a wealth of practical information from across the liter 410 0$aWiley Series on Radiochemical Syntheses 606 $aRadiopharmaceuticals$xSynthesis 606 $aTomography, Emission 615 0$aRadiopharmaceuticals$xSynthesis. 615 0$aTomography, Emission. 676 $a616.07575 701 $aScott$b Peter J. H$0934605 701 $aHockley$b Brian G$01701913 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910815201303321 996 $aRadiochemical synthesis$94086013 997 $aUNINA LEADER 01646nam2 2200325 450 001 996675482503316 005 20250917104424.0 010 $a978-88-93464-03-1 100 $a20250820d2020----km y0itay5003 ba 101 2 $aita$alat 102 $aIT 105 $ay 00 y 200 1 $aEpitalamio per Massimo$evir spectabilis$fMagno Felice Ennodio$ga cura di Marino Neri 210 $aMilano$cLa vita felice$d2020 215 $a185 p.$d17 cm 225 2 $aSaturnalia$v52 300 $aTesto originale a fronte 330 $aL?epitalamio è un canto nuziale, un sottogenere lirico greco imitato più tardi dai Romani, destinato a celebrare in versi un matrimonio, presso la camera degli sposi. Nelle poesie, benché una volta protesti contro le falsità degli antichi e invochi lo Spirito Santo, Ennodio non sdegna di rappresentare Apollo, Venere, le Muse: nell?epitalamio per Massimo, Amore si lamenta con Venere dell?ascetismo introdotto dal cristianesimo. Il poeta più imitato è Virgilio; i sette mediocri inni religiosi arieggiano quelli di sant?Ambrogio. Un epitalamio in chiave di conversione, quella di Massimo, dalla precedente vita ascetica a quella coniugale. (Fonte: editore) 410 0$1001996673680003316$12001$aSaturnalia$v, 52 500 10$aEpithalamium dictum Maximo$94435031 676 $a871.02 700 1$aENNODIUS,$bMagnus Felix$0220646 702 1$aNERI,$bMarino$f<1976- > 801 0$aIT$bcba$gREICAT 912 $a996675482503316 951 $aV.3. Coll. 29/ 52$b292258 L.M.$cV.3. Coll.$d573444 959 $aBK 969 $aUMA 996 $aEpithalamium dictum Maximo$94435031 997 $aUNISA