LEADER 01006nac--2200325---450- 001 990005827930203316 005 20130411112342.0 035 $a000582793 035 $aUSA01000582793 035 $a(ALEPH)000582793USA01 035 $a000582793 100 $a20130411d1961----km-y0itay50------ba 101 0 $aita 102 $aIT 105 $ay|||z|||001yy 200 1 $aNote critiche al testo del De nuncio sagaci$fAgostino Pastorino 210 $aSiracusa$cIstituto nazionale del dramma antico$d1961 215 $a14 p.$d24 cm 300 $aGià pubblicato in: Dioniso, anno 35, fasc. 3-4 (lug.-dic. 1961) 676 $a872.03 700 1$aPASTORINO,$bAgostino$0162529 801 0$aIT$bsalbc$gISBD 912 $a990005827930203316 951 $aXV.8. 1615$b226276 L.M.$cXV.8. 959 $aBK 969 $aFSO 979 $aANNAMARIA$b90$c20130411$lUSA01$h1010 979 $aANNAMARIA$b90$c20130411$lUSA01$h1123 996 $aNote critiche al testo del De nuncio sagaci$91514124 997 $aUNISA LEADER 01303nam0 22003133i 450 001 UFI0317503 005 20231121125907.0 020 $aIT$b1931 5286 100 $a20210412d1931 ||||0itac50 ba 101 | $aita 102 $ait 181 1$6z01$ai $bxxxe 182 1$6z01$an 200 1 $a˜Le œforme poetiche dei greci e dei romani$ecompendio di metrica classica con riferimenti alla versificazione italiana per le scuole e per gli studiosi$fCesare Bione 210 $aFirenze$cLa Nuova Italia$dstampa 1931 215 $aVIII, 191 p.$d20 cm. 606 $aPoesia classica$xMetrica$2FIR$3RMLC463222$9N 676 $a808.1$9Retorica della poesia.$v22 676 $a871.01$9Poesia latina. 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Periodo antico, fino al 499 ca.$v22 700 1$aBione$b, Cesare$3RAVV079221$4070$0185766 801 3$aIT$bIT-01$c20210412 850 $aIT-FR0017 899 $aBiblioteca umanistica Giorgio Aprea$bFR0017 $eN 912 $aUFI0317503 950 0$aBiblioteca umanistica Giorgio Aprea$d 52DLM N /32 /$e 52DUP0009053315 VMC RS $fC $h20210506$i20210506 977 $a 52 996 $aForme poetiche dei Greci e dei Romani$93365581 997 $aUNICAS LEADER 03114nam 22005655 450 001 9910781518303321 005 20200706234447.0 010 $a1-283-45159-X 010 $a9786613451590 010 $a3-642-23294-9 024 7 $a10.1007/978-3-642-23294-7 035 $a(CKB)2550000000075197 035 $a(EBL)885237 035 $a(OCoLC)769756129 035 $a(SSID)ssj0000610579 035 $a(PQKBManifestationID)11434903 035 $a(PQKBTitleCode)TC0000610579 035 $a(PQKBWorkID)10639421 035 $a(PQKB)10500187 035 $a(DE-He213)978-3-642-23294-7 035 $a(MiAaPQ)EBC885237 035 $a(PPN)15750705X 035 $a(EXLCZ)992550000000075197 100 $a20111206d2012 u| 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aPractical Handbook for Small-Gauge Vitrectomy$b[electronic resource] $eA Step-By-Step Introduction to Surgical Techniques /$fby Ulrich Spandau, Heinrich Heimann 205 $a1st ed. 2012. 210 1$aBerlin, Heidelberg :$cSpringer Berlin Heidelberg :$cImprint: Springer,$d2012. 215 $a1 online resource (197 p.) 300 $aAuthorized translation of the 1st German language edition copyright 2009 by Kaden-Verlag, Heidelberg. 311 $a3-642-23293-0 320 $aIncludes bibliographical references and index. 327 $aIntroduction to small-gauge vitrectomy -- Equipment -- General considerations and techniques of pars plana vitrectomy -- Special techniques for pars plana vitrectomy -- Conventional vitrectomy with 3-port trocar system -- Bimanual vitrectomy with 4-port trocar system -- Diabetic retinopathy -- Dislocated IOL and dropped nucleus -- Endophthalmitis -- Detachment -- Trauma -- Surgical pearls -- Appendix. 330 $aSince the development of 23G vitrectomy in 2004, the technique has revolutionized retinal surgery by overcoming a number of the problems associated with 20G and 25G systems and offering significant improvements in surgical capability and fluidics. This important book first discusses the instruments and equipment employed in 23G vitrectomy and then explains, step by step, the various surgical techniques with the aid of informative diagrams and many high-quality photos. In addition, videos are included that document the different procedures, from the straightforward to the demanding. This book will serve as an immensely useful guide for all surgeons who are intending to make use of this exciting and increasingly used technique. 606 $aOphthalmology 606 $aOphthalmology$3https://scigraph.springernature.com/ontologies/product-market-codes/H44004 615 0$aOphthalmology. 615 14$aOphthalmology. 676 $a617.7/46 676 $a617.746 700 $aSpandau$b Ulrich$4aut$4http://id.loc.gov/vocabulary/relators/aut$0755418 702 $aHeimann$b Heinrich$4aut$4http://id.loc.gov/vocabulary/relators/aut 906 $aBOOK 912 $a9910781518303321 996 $aPractical Handbook for Small-Gauge Vitrectomy$91754594 997 $aUNINA LEADER 05574nam 2200697 450 001 9910830571203321 005 20221231053559.0 010 $a3-527-68172-8 010 $a3-527-68780-7 010 $a3-527-68174-4 035 $a(CKB)3710000000121872 035 $a(EBL)1701417 035 $a(SSID)ssj0001322276 035 $a(PQKBManifestationID)11862279 035 $a(PQKBTitleCode)TC0001322276 035 $a(PQKBWorkID)11424953 035 $a(PQKB)10428054 035 $a(MiAaPQ)EBC1701417 035 $a(MiAaPQ)EBC4044587 035 $a(MiAaPQ)EBC7041985 035 $a(Au-PeEL)EBL7041985 035 $a(PPN)220885028 035 $a(EXLCZ)993710000000121872 100 $a20221231d2014 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 10$aSide reactions in organic synthesis II $earomatic substitutions /$fFlorencio Zaragoza Do?rwald 205 $aSecond edition. 210 1$aWeinheim, Germany :$cWiley-VCH Verlag GmbH & Co. KGaA,$d[2014] 210 4$d©2014 215 $a1 online resource (311 p.) 300 $aDescription based upon print version of record. 311 $a3-527-33721-0 320 $aIncludes bibliographical references and index. 327 $aSide Reactions in Organic Synthesis II; Contents; Preface; Glossary and Abbreviations; Journal Abbreviation List; Chapter 1 Electrophilic Alkylation of Arenes; 1.1 General Aspects; 1.1.1 Catalysis by Transition-Metal Complexes; 1.1.2 Typical Side Reactions; 1.2 Problematic Arenes; 1.2.1 Electron-Deficient Arenes; 1.2.2 Phenols; 1.2.3 Anilines; 1.2.4 Azoles; 1.3 Problematic Electrophiles; 1.3.1 Methylations; 1.3.2 Olefins; 1.3.3 Allylic Electrophiles; 1.3.4 Epoxides; 1.3.5 ?-Haloketones and Related Electrophiles; 1.3.6 Nitroalkanes; 1.3.7 Ketones; 1.3.8 Alcohols; References 327 $aChapter 2 Electrophilic Olefination of Arenes2.1 General Aspects; 2.2 Olefinations with Leaving-Group-Substituted Olefins; 2.3 Olefinations with Unsubstituted Olefins; 2.4 Olefinations with Alkynes; References; Chapter 3 Electrophilic Arylation of Arenes; 3.1 General Aspects; 3.2 Arylations with Aryl Halides; 3.2.1 Via Cationic Intermediates; 3.2.2 Via Radicals; 3.2.3 Via Transition-Metal Chelates; 3.2.4 By Transition-Metal Catalysis; 3.3 Arylations with Diazonium Salts; 3.4 Arylations with Other Functionalized Arenes; 3.5 Arylations with Unsubstituted Arenes; References 327 $aChapter 4 Electrophilic Acylation of Arenes4.1 General Aspects; 4.2 Problematic Arenes; 4.2.1 Dealkylation/Isomerization of Arenes; 4.2.2 Styrenes; 4.2.3 Anilines, Phenols, and Thiophenols; 4.2.4 Electron-Deficient Arenes; 4.2.5 Azoles; 4.3 Problematic Electrophiles; 4.3.1 Problematic Acyl Halides; 4.3.2 Carboxylic Esters and Lactones; 4.3.3 Carbonic Acid Derivatives; 4.3.4 Formic Acid Derivatives; 4.3.5 Mixed Carboxylic Anhydrides and Other Polyelectrophiles; References; Chapter 5 Electrophilic Halogenation of Arenes; 5.1 General Aspects; 5.2 Typical Side Reactions; 5.3 Regioselectivity 327 $a5.4 Catalysis5.5 Fluorinations; 5.6 Electron-Deficient Arenes; 5.6.1 Pyridines; 5.6.2 Benzoic Acid Derivatives; 5.7 Electron-Rich Arenes; 5.7.1 Phenols and Arylethers; 5.7.2 Anilines; 5.7.3 Azoles; 5.8 Sensitive Functional Groups; 5.8.1 Alkenes; 5.8.2 Amines; 5.8.3 Ethers; 5.8.4 Thiols and Thioethers; 5.8.5 Aldehydes, Ketones, and Other C-H Acidic Compounds; 5.8.6 Amides; References; Chapter 6 Electrophilic Formation of Aromatic C-N Bonds; 6.1 Nitration of Arenes; 6.1.1 Mechanisms; 6.1.2 Regioselectivity; 6.1.3 Catalysis; 6.1.4 Electron-Deficient Arenes; 6.1.5 Electron-Rich Arenes 327 $a6.1.5.1 Anilines6.1.5.2 Indoles; 6.1.5.3 Phenols; 6.2 Electrophilic Aromatic Aminations; 6.2.1 Typical Side Reactions; 6.3 Electrophilic Aromatic Amidations; 6.3.1 Typical Side Reactions; References; Chapter 7 Electrophilic Formation of Aromatic C-S Bonds; 7.1 Sulfonylation; 7.1.1 General Aspects; 7.1.2 Typical Side Reactions; 7.2 Sulfinylation; 7.2.1 General Aspects; 7.2.2 Typical Side Reactions; 7.3 Sulfenylation; 7.3.1 General Aspects; 7.3.2 Typical Side Reactions; References; Chapter 8 Aromatic Nucleophilic Substitutions; 8.1 General Aspects; 8.1.1 Mechanisms; 8.1.2 Regioselectivity 327 $a8.1.3 Acid-/Base-Catalysis 330 $aFollowing in the footsteps of the successful ""Side Reactions in Organic Synthesis"" by the same, highly experienced author, this new textbook focuses on aromatic substitution reactions, both electrophilic and nucleophilic.The coverage is reader-friendly with each chapter dealing with a certain reaction class in terms of its scope and limitations in detail, and unique in its approach since unexpected and unwanted side reactions are hard to find in the literature.A valuable addition to the classical textbooks on organic chemistry, this is a must-have for graduate students as well as for 517 3 $aSide reactions in organic synthesis 2 517 3 $aSide reactions in organic synthesis two 606 $aAromatic compounds$xSynthesis 606 $aOrganic compounds$xSynthesis 606 $aAromatic compounds 615 0$aAromatic compounds$xSynthesis. 615 0$aOrganic compounds$xSynthesis. 615 0$aAromatic compounds. 676 $a547.6 700 $aDo?rwald$b Florencio Zaragoza$0875082 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910830571203321 996 $aSide reactions in organic synthesis II$94085328 997 $aUNINA