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[null,"1.","Record Nr.",null,"UNINA990008342450403321"]
[null,null,"Autore",null,"Pavanello, Giuseppe <1947- >"]
[null,null,"Titolo",null,"Tiziano : restauri,tecniche,programmi,prospettive / a cura di Giuseppe Pavanello"]
[null,null,"Pubbl/distr/stampa",null,"Venezia : Istituto Veneto di Scienze, Lettere ed Arti, 2005"]
[null,null,"ISBN",null,"88-88143-40-8"]
[null,null,"Descrizione fisica",null,"215 p. : ill. ; 24 cm"]
[null,null,"Collana",null,"Studi di arte veneta ; 9"]
[null,null,"Disciplina",null,"759.5"]
[null,null,"Locazione",null,"FLFBC"]
[null,null,"Collocazione",null,"759.5 CONV VENEZIA 1"]
[null,null,"Lingua di pubblicazione",null,"Italiano"]
[null,null,"Formato",null,"Materiale a stampa"]
[null,null,null,"Livello bibliografico","Monografia"]
[null,null,null,"Note generali","Il volume riporta le relazioni presentate al seminario di studio \"Restauri dei dipinti di Tiziano.Tecniche,programmi e prospettive\"(Venezia,3-4 aprile 2000)"]
[null,"2.","Record Nr.",null,"UNINA9910830529703321"]
[null,null,"Autore",null,"Brown D. J"]
[null,null,"Titolo",null,"Quinazolines Supplement I [[electronic resource] /] / D.J. Brown"]
[null,null,"Pubbl/distr/stampa",null,"New York, : J. Wiley, c1996"]
[null,null,"ISBN",null,"1-282-30612-X"]
[{"$nulls":4},"9786612306129"]
[{"$nulls":4},"0-470-18795-6"]
[{"$nulls":4},"0-470-18894-4"]
[null,null,"Descrizione fisica",null,"1 online resource (760 p.)"]
[null,null,"Collana",null,"Chemistry of heterocyclic compounds ; ; v. 55"]
[null,null,"Disciplina",null,"547.593"]
[{"$nulls":4},"547/.59/05"]
[{"$nulls":4},"547/.593"]
[null,null,"Soggetti",null,"Quinazoline"]
[{"$nulls":4},"Heterocyclic compounds"]
[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","\"An Interscience publication.\""]
[null,null,null,"Nota di bibliografia","Includes bibliographical references (p. 607-681) and index."]
[null,null,"Nota di contenuto",null,"QUINAZOLINES; Contents; CHAPTER 1. PRIMARY SYNTHESES; 1.1 From a Single Benzene Substrate; 1.1.1 By Formation of the 1,2-Bond; 1.1.2 By Formation of the 1,Sa-Bond; 1.1.3 By Formation of the 2,3-Bond; 1.1.3.1. From o-Acylaminobenzamides; 1.1.3.2 From o-Acylaminobenzamide Oximes; 1.1.3.3 From o-(A1koxycarbonylamino)-benzamides; 1.1.3.4 From o-Ureidobenzamides; 1.1.3.5 From o-(Benzylideneamino)benz-amides; 1.1.3.6 From o-Acylaminobenzonitriles; 1.1.3.7 From o-(Substituted Methylene-amin0)benzonitriles; 1.1.3.8 From o-(Acylamino)benzaldehyde Hydrazones and Related Substrates"]
[{"$nulls":4},"1.1.3.9 From Miscellaneous Substrates1.1.4 By Formation of the 3,4-Bond; 1.1.4.1 From o-Ureidobenzoic Acids; 1.1.4.2 From o-Ureidobenzoic Esters; 1.1.4.3 From o-Ureidobenzoyl Chlorides or o-Ureidobenzamides; 1.1.4.4 From o-Ureidobenzonitriles; 1.1.4.5 From o- U reidobenzaldehyde Derivatives and Related Substrates; 1.1.4.6 From o-(Aminomethy1eneamino)-benzoic Acids, Esters, or Amides; 1.1.4.7 From Miscellaneous Substrates; 1.1.5 By Formation of the 4,4a-Bond; 1.2 From a Benzene Substrate and Ancillary Synthon(s); 1.2.1 Where the Synthon Supplies N1; 1.2.2 Where the Synthon Supplies C2"]
[{"$nulls":4},"1.2.2.1 The Use of Carboxylic Acids and Related Synthons1.2.2.2 The Use of Carbonic Acid-Derived Synthons; 1.2.3 Where the Synthon "]
[{"$nulls":4},"Supplies N3; 1.2.3.1 With o-Acylaminobenzoic Acids as Substrates; 1.2.3.2 With o-Acylaminobenzoic Esters as Substrates; 1.2.3.3 With o-Acylaminobenzonitriles as Substrates; 1.2.3.4 With o-Acylaminobenzaldehydes or Related Ketones as Substrates; 1.2.3.5 With o-(Alkoxycarbony1amino)-benzoic Esters or Related Ketones as Substrates; 1.2.3.6 With o-(Substituted Methylene-amino)benzoic Esters or Related Ketones as Substrates"]
[{"$nulls":4},"1.2.3.7 With o-(Substituted Methylene-amin0)benzonitriles as Substrates1.2.3.8 With o-Isocyanatobenzoyl Chlorides as Substrates; 1.2.3.9 With o-Isocyanatobenzoic Esters and Related Ketones or Nitriles as Substrates; 1.2.3.10 With o-Cyanoamino- or o-Ureido-benzoic Esters and Related Ketones or Nitriles as Substrates; 1.2.3.11 With Miscellaneous Substrates; 1.2.4 Where the Synthon Supplies C4; 1.2.5 Where the Synthon(s) Supply N1 + C2; 1.2.6 Where the Synthon(s) Supply C2 + N3; 1.2.6.1 With o-Aminobenzoic Acids as Substrates; 1.2.6.2 With o-Aminobenzoic Esters as Substrates"]
[{"$nulls":4},"1.2.6.3 With o-Aminobenzarnides as Substrates1.2.6.4 With o-Arninobenzonitriles as Substrates; 1.2.6.5 With o-Aminobenzaldehydes or Related Ketones as Substrates; 1.2.6.6 With Miscellaneous o-Disubstitu-ted Benzenes as Substrates; 1.2.7 Where the Synthon(s) Supply N3 + C4; 1.2.7.1 With N-Acylanilines as Substrates; 1.2.7.2 With N-(α-Chloromethy1ene)ani-lines or Related Compounds as Substrates; 1.2.7.3 With Other Aniline Derivatives as Substrates; 1.2.8 Where the Synthon(s) Supply N1+C2 + N3; 1.2.8.1 With o-Halogeno or o-Alkoxyben-zonitriles as Substrates"]
[{"$nulls":4},"1.2.8.2 With o-Substituted Benzoic Esters or Related Compounds as Substrates"]
[null,null,null,"Sommario/riassunto","Primary Syntheses. Quinazoline, Alkylquinazolines, and Arylquinazolines. Halogenoquinazolines. Oxyquinazolines. Thioquinazolines. Nitro, Amino, and Related Quinazolines. Quinazolinecarboxylic Acids and Related Derivatives. Appendix. References. Index."]