01074cam0 2200265 450 E60020006035120201123140412.020100223d1972 |||||ita|0103 baitaITCoscienza ed autocoscienza in HegelMario OlivieriPadovaCEDAM1972112 p.25 cmPubblicazioni della Scuola di perfezionamento in filosofia dell'Università di PadovaQuaderni di storia della filosofia4001LAEC000282052001 *Pubblicazioni della Scuola di perfezionamento in filosofia dell'Università di Padova. Quaderni di storia della filosofia4Olivieri, MarioA60020005994307023410ITUNISOB20201123RICAUNISOBUNISOB10070536E600200060351M 102 Monografia moderna SBNM100007669Si70536acquistopregresso3UNISOBUNISOB20100223092833.020201123140400.0AlfanoCoscienza ed autocoscienza in Hegel1704037UNISOB01566oam 2200445Ka 450 991069646630332120080304115734.0(CKB)5470000002378177(OCoLC)212746972(OCoLC)995470000002378177(EXLCZ)99547000000237817720080304d1999 ua 0engtxtrdacontentcrdamediacrrdacarrierReal-time monitoring of active landslides[electronic resource] /Mark E. Reid, Richard G. LaHusen, William L. Ellis[Reston, Va.] :U.S. Dept. of the Interior, U.S. Geological Survey,[1999]2 unnumbered pages digital, PDF fileU.S. Geological Survey fact sheet ;091-99Title from title screen (viewed on Mar. 4, 2008).Real time monitoring of active landslidesReducing landslide hazards in the United StatesLandslide hazard analysisCaliforniaLandslidesResearchCaliforniaDebris avalanchesCaliforniaLandslide hazard analysisLandslidesResearchDebris avalanchesReid Mark E1381376LaHusen Richard G1385062Ellis William L1385399Geological Survey (U.S.)GPOGPOGPOBOOK9910696466303321Real-time monitoring of active landslides3543592UNINA05574nam 2200697 450 991083057120332120221231053559.03-527-68172-83-527-68780-73-527-68174-4(CKB)3710000000121872(EBL)1701417(SSID)ssj0001322276(PQKBManifestationID)11862279(PQKBTitleCode)TC0001322276(PQKBWorkID)11424953(PQKB)10428054(MiAaPQ)EBC1701417(MiAaPQ)EBC4044587(MiAaPQ)EBC7041985(Au-PeEL)EBL7041985(PPN)220885028(EXLCZ)99371000000012187220221231d2014 uy 0engur|n|---|||||txtccrSide reactions in organic synthesis II aromatic substitutions /Florencio Zaragoza DörwaldSecond edition.Weinheim, Germany :Wiley-VCH Verlag GmbH & Co. KGaA,[2014]©20141 online resource (311 p.)Description based upon print version of record.3-527-33721-0 Includes bibliographical references and index.Side 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 α-Haloketones and Related Electrophiles; 1.3.6 Nitroalkanes; 1.3.7 Ketones; 1.3.8 Alcohols; ReferencesChapter 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; ReferencesChapter 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 Regioselectivity5.4 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 Arenes6.1.5.1 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 Regioselectivity8.1.3 Acid-/Base-CatalysisFollowing 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 forSide reactions in organic synthesis 2Side reactions in organic synthesis twoAromatic compoundsSynthesisOrganic compoundsSynthesisAromatic compoundsAromatic compoundsSynthesis.Organic compoundsSynthesis.Aromatic compounds.547.6Dörwald Florencio Zaragoza875082MiAaPQMiAaPQMiAaPQBOOK9910830571203321Side reactions in organic synthesis II4085328UNINA