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[null,"1.","Record Nr.",null,"UNISA990001339870203316"]
[null,null,"Autore",null,"BALZAC, Honoré : de"]
[null,null,"Titolo",null,"Ursule Mirouet / Honoré de Balzac ; avec une introduction et des notes par Maurice Allem"]
[null,null,"Pubbl/distr/stampa",null,"Paris, : Garnier, 1952"]
[null,null,"Descrizione fisica",null,"IX, 325 p. ; in 16°, 19 cm"]
[null,null,"Collana",null,"Classiques Garnier"]
[null,null,"Collocazione",null,"VI.4.A. 275 (II f A 12)"]
[null,null,"Lingua di pubblicazione",null,"Francese"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,"2.","Record Nr.",null,"UNINA9910132195403321"]
[null,null,"Titolo",null,"Progress in inorganic chemistry . Volume 59 / / edited by Kenneth D. Karlin"]
[null,null,"Pubbl/distr/stampa",null,"Hoboken, New Jersey : , : John Wiley & Sons, Inc., , 2014"]
[{"$nulls":4},"©2014"]
[null,null,"ISBN",null,"1-118-87003-4"]
[{"$nulls":4},"1-118-86999-0"]
[{"$nulls":4},"1-118-86988-5"]
[null,null,"Descrizione fisica",null,"1 online resource (593 p.)"]
[null,null,"Collana",null,"Progress in Inorganic Chemistry"]
[null,null,"Disciplina",null,"546.851"]
[null,null,"Soggetti",null,"Chemistry, Inorganic - Experiments"]
[{"$nulls":4},"Chemistry, Inorganic"]
[{"$nulls":4},"Electronic books."]
[null,null,"Lingua di pubblicazione",null,"Inglese"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,null,null,"Note generali","Description based upon print version of record."]
[null,null,null,"Nota di bibliografia","Includes bibliographical references and indexes."]
[null,null,"Nota di contenuto",null,"Progress in Inorganic Chemistry; Contents; Chapter 1: Iron Catalysis in Synthetic Chemistry; I. INTRODUCTION; II. ADDITION REACTIONS; A. Cycloadditions; 1. The [2+2] Cycloaddition; 2. The [3+2] Cycloaddition; 3. The [2+2+2] Cycloaddition; 4. The [4+2] Cycloaddition; B. Cyclopropanation; C. Aziridination and Aziridine Ring-Opening Reactions; D. Carbometalation of C-C Unsaturated Bond; E. Michael Addition; F. Barbier-Type Reaction; G. Kharasch Reaction; III. THE C-C BOND FORMATIONS VIA C-H FUNCTIONALIZATION; A. The C-H Arylation; 1. Direct Arylation With Organometallic Reagents"]
[{"$nulls":4},"2. Direct Arylation With Aryl HalidesB. The C-C Bond Formation Via Cross-Dehydrogenative Coupling; 1. The CDC Between Two sp3 C-H Bonds; 2. The CDC Between sp3 and sp2 C-H Bonds; 3. The CDC Between sp3 and sp C-H Bonds; C. The C-C Bond Formation via Cross-Decarboxylative Coupling; D. The C-C Bond Formation via Alkene Insertion; E. Oxidative Coupling of Two C-H Bonds; IV. THE C-H BOND OXIDATION; A. Hydroxylation; B. Epoxidation; C. cis-Dihydroxylation; V. CROSS-COUPLING REACTIONS; A. Alkenyl Derivatives as Coupling Partners; B. Aryl Derivatives as Coupling Partners"]
[{"$nulls":4},"C. Alkyl Derivatives as Coupling Partners1. Low-Valent Iron Complex in Cross-Coupling Reactions; D. Acyl Derivatives as Coupling Partners; E. Iron-Catalyzed C-O, C-S, and C-N Cross-Coupling Reaction; F. Iron-"]
[{"$nulls":4},"Catalyzed Mizoraki-Heck Reaction; G. Iron-Catalyzed Negishi Coupling Reaction; H. Suzuki-Miyaura Coupling Reaction; I. Sonogashira Reaction; J. Mechanism of Cross-Coupling Reactions; K. Hydrocarboxylation; L. Enyne Cross-Coupling Reaction; VI. DIRECT C-N BOND FORMATION VIA C-H OXIDATION; VII. IRON-CATALYZED AMINATION; A. Allylic Aminations; B. Intramolecular Allylic Amination"]
[{"$nulls":4},"VIII. SULFOXIDATIONS AND SYNTHESIS OF SULFOXIMINES, SULFIMIDES, AND SULFOXIMIDESA. Sulfoxidation; B. Synthesis of Sulfoximines, Sulfimides, and Sulfoximides; 1. Mechanism; IX. REDUCTION REACTIONS; A. Hydrosilylation of Alkenes; B. Hydrosilylation of Aldehydes and Ketones; C. Hydrogenation of C-C Unsaturated Bonds; D. Hydrogenation of Ketones; E. Hydrogenation of Imines; F. Reduction of Nitroarene to Anilines; G. Hydrogenation of Carbon Dioxide and Bicarbonate; H. Amide Reduction; I. Reductive Aminations; X. TRIFLUOROMETHYLATION; XI. CONCLUSION; ACKNOWLEDGMENTS; ABBREVIATIONS; REFERENCES"]
[{"$nulls":4},"Chapter 2: A New Paradigm for Photodynamic Therapy Drug Design: Multifunctional, Supramolecular DNA Photomodification Agents Featuring Ru(II)/Os(II) Light Absorbers Coupled to Pt(II) or Rh(III) Bioactive SitesI. INTRODUCTION; A. Scope and Limitations; B. Cancer; C. Deoxyribonucleic Acid as a Target; II. PHOTODYNAMIC THERAPY; A. Requirements; B. Traditional PDT Agents; C. Ruthenium(II) Light Absorbers as PDT Agents; III. PLATINUM AND RHODIUM CENTERS AS BIOACTIVE SITES; A. Platinum(II) Based Chemotherapeutics; 1. Cisplatin; 2. Second and Third Generation Pt(II) Drugs"]
[{"$nulls":4},"B. Rhodium as a Bioactive Site"]
[null,null,null,"Sommario/riassunto","This series provides inorganic chemists and materials scientists with a forum for critical, authoritative evaluations of advances in every area of the discipline. Volume 59 continues to report recent advances with a significant, up-to-date selection of contributions by internationally-recognized researchers.  The chapters of this volume are devoted to the following topics:  Iron Catalysis in Synthetic Chemistry A New Paradigm for Photodynamic Therapy Drug Design: Multifunctional, Supramolecular DNA Photomodification Agents Featuring Ru(II)/Os(II) Light Absorbers Coupled t"]
[null,"3.","Record Nr.",null,"UNINA9910563069303321"]
[null,null,"Autore",null,"Celunova Elena A"]
[null,null,"Titolo",null,"Psaltyr' 1683 goda v perevode Avramija Firsova / Elena A. Celunova"]
[null,null,"Pubbl/distr/stampa",null,"Frankfurt a.M, : PH02, 1989"]
[null,null,"Edizione",null,"[1st, New ed.]"]
[null,null,"Descrizione fisica",null,"1 online resource (652 p.) : , EPDF"]
[null,null,"Collana",null,"Slavistische Beiträge ; 243"]
[null,null,"Soggetti",null,"linguistics"]
[null,null,"Lingua di pubblicazione",null,"Tedesco"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,null,null,"Note generali","Peter Lang GmbH, Internationaler Verlag der Wissenschaften"]
[null,null,"Nota di contenuto",null,"Предисловие - Примечания - Лигература - Об издании текста - Приложeниe No.1: \"Apгyмeнтьi\" - Приложeниe No.2: Укaзaтeль cлoв и фopм к Пcaльгpи A. Фиpcoвa 1683 гoдa"]
[null,null,null,"Sommario/riassunto","Vpervye izdavaemaja Psaltyr' 1683 goda v perevode Avramija Firsova (...) javljaetsja unikal'nym pamjatnikom pis'mennosti konca XVII veka... Eto pervaja v Moskovskij Rusi popytka perevoda teksta Svjaščennogo Pisanija na jazyk, otličnyj ot kanoničeskogo cerkovnoslavjanskogo."]