01122cam0-22003971i-450-99000711709040332120110928120214.088-14-09446-2000711709FED01000711709(Aleph)000711709FED0100071170920020913d2001----km-y0itay50------baitaITy---n---001yySindacato in Europala confederazione europea dei sindacati di fronte alle sfide della moneta unica e dell'allargamento ad est dell'UERoberta NuninMilanoGiuffrè2001X, 125 p.23 cmSindacatiEuropa331.8809421ita34420itaNunin,Roberta146958ITUNINARICAUNIMARCBK990007117090403321DPR 28-81919908DECXIV G 30843122FSPBCB-IX-63DDRCQ 4942763DSIDECDDRCDSIFSPBCSindacato in Europa702863UNINA01037nas 2200337- 450 991022594670332120230330000244.0(CKB)3710000000888624(CONSER)--2016210848(EXLCZ)99371000000088862420160201a20169999 --- aengtxtrdacontentcrdamediacrrdacarrierMEED business review[London] :MEED Media,2016-1 online resourcePrint version: MEED business review. 2397-7310 (DLC) 2016210848 (OCoLC)940258973 Economic historyfast(OCoLC)fst00901974Middle EastEconomic conditions1945-PeriodicalsMiddle EastfastPeriodicals.fastPeriodicals.lcgftEconomic history.330.956/005JOURNAL9910225946703321exl_impl conversionMEED business review2099473UNINA01068nam a22002651i 450099100211169970753620040126141630.0040407s1972 it a||||||||||||||||ita b12872404-39ule_instARCHE-085202ExLDip.to Scienze StoricheitaA.t.i. Arché s.c.r.l. Pandora Sicilia s.r.l.741.946Mostra di disegni spagnoli /introduzione e catalogo di Alfonso E. Pérez SánchezFirenze :Leo S. Olschki,1972123 p. :ill. ;24 cmGabinetto disegni e stampe degli Uffizi ;37Disegni spagnoliMostrePérez Sánchez, Alfonso EmilioGabinetto disegni e stampe degli Uffizi <Firenze>.b1287240402-04-1416-04-04991002111699707536LE009 ARTE 709-4112009000325319le009-E0.00-l- 00000.i1343338616-04-04Mostra di disegni spagnoli299967UNISALENTOle00916-04-04ma -itait 0101590nam 2200397 450 991014705270332120231020005504.00-7381-4688-9(CKB)1000000000035346(NjHacI)991000000000035346(EXLCZ)99100000000003534620231020d2005 uy 0engur|||||||||||txtrdacontentcrdamediacrrdacarrierIEEE standard for local and metropolitan area networks station and media access control connectivity discovery /IEEE Computer Society LAN/MAN Standards CommitteeNew York, N.Y. :Institute of Electrical and Electronics Engineers,2005.1 online resource (xii, 158 pages) illustrations0-7381-4687-0 This document defines a protocol and a set of managed objects that can be used for discovering the physical topology from adjacent stations in IEEE 8020 LANs.IEEE Std 802.1AB-2005Local area networks (Computer networks)Metropolitan area networks (Computer networks)Local area networks (Computer networks)Metropolitan area networks (Computer networks)004.68Institute of Electrical and Electronics Engineers,IEEE-SA Standards Board,NjHacINjHaclDOCUMENT9910147052703321IEEE standard for local and metropolitan area networks2574840UNINA05279oam 2200505 450 991029865930332120190911112725.03-319-01324-610.1007/978-3-319-01324-4(OCoLC)881096887(MiFhGG)GVRL6WLD(EXLCZ)99371000000007874420130715d2014 uy 0engurun|---uuuuatxtccrDevelopment of new radical cascades and multi-component reactions application to the synthesis of nitrogen-containing heterocycles /Marie-Helene Larraufie1st ed. 2014.Cham [Switzerland] :Springer,2014.1 online resource (xxii, 326 pages) illustrations (some color)Springer Theses, Recognizing Outstanding Ph.D. Research,2190-5053"ISSN: 2190-5053."3-319-01323-8 Includes bibliographical references at the end of each chapters.INTRODUCTION -- PART A: N-ACYLCYANAMIDES AS NEW PARTNERS IN RADICAL CASCADES: SYNTHESIS OF POLYCYCLIC QUINAZOLINONES AND GUANIDINES -- THE CYANAMIDE MOIETY, SYNTHESIS AND REACTIVITY -- HOMOLYTIC AROMATIC SUBSTITUTIONS: STATE OF THE ART OF THE MECHANISTIC PROPOSALS -- RESULTS: DEVELOPMENTS OF NEW RADICAL CASCADES WITH N-ACYLCYANAMIDES -- OBJECTIVES OF THE PROJECT -- ADDITION OF ALKYL RADICALS -- ADDITION OF VINYL RADICALS TO N-ACYLCYANAMIDES -- ADDITION OF NITROGEN CENTERED RADICALS -- PREPARATION AND CYCLIZATION OF ALKYL PRECURSORS -- PREPARATION AND CYCLIZATION OF VINYL PRECURSORS -- PREPARATION AND CYCLIZATION OF AZIDE PRECURSORS -- PART B: VISIBLE-LIGHT PHOTOREDUCTIVE CATALYSIS FOR AN ECO-COMPATIBLE GENERATION OF RADICALS -- BIBLIOGRAPHICAL BACKGROUNDS: GENERATION OF RADICALS BY VISIBLE LIGHT PHOTOREDOX CATALYSIS -- PHOTOPHYSICAL PROPERTIES OF TRIS(BIPYRIDYL)RUTHENIUM(II) COMPLEXES -- STATE OF THE ART OF THE SUBSTRATES AMENABLE TO VISIBLE LIGHT PHOTOREDOX CATALYSIS -- RESULTS: VISIBLE LIGHT-INDUCED PHOTOREDUCTIVE GENERATION OF RADICALS FROM EPOXIDES AND AZIRIDINES -- EPOXIDES AS NEW SUBSTRATES FOR VISIBLE-LIGHT TRIGGERED GENERATION OF RADICALS -- SCOPE AND LIMITATIONS OF THE REDUCTIVE RING-OPENING METHODOLOGY -- UTILIZATION OF THE PHOTOGENERATED RADICALS IN CARBON-CARBON BOND FORMATIONS -- SUPPORTING INFORMATION -- GENERAL REMARKS -- GENERAL PROCEDURES -- EPOXIDE, AZIRIDINES AND CYCLOPROPANES PRECURSORS -- REDUCTIVE RING-OPENING PRODUCTS -- ALLYLATION PRODUCTS 246 -- PART C: NEW DEVELOPMENTS IN ARYL-ARYL COUPLINGS VIA PALLADIUM/NORBORNENE DUAL CATALYSIS: SYNTHESIS OF PHENANTHRIDINES AND PHENANTHRENES -- BIBLIOGRAPHICAL BACKGROUND: THE ORTHO EFFECT IN THE CATELLANI REACTION -- THE CATELLANI REACTION -- SYNTHETIC APPLICATIONS OF THE ORTHO EFFECT -- MECHANISTIC EXPLANATIONS FOR THE ORTHO EFFECT -- RESULTS: NEW PARTNERS FOR ORTHO-SUBSTITUTED ARYL IODIDES IN PALLADIUM/NORBORNENE COCATALYSIS -- COUPLING OF ORTHO-SUBSTITUTED ARYL IODIDES AND BROMOBENZYL AMINES: FIRST REPORTED CATELLANI SEQUENCE TERMINATED BY N-ARYL COUPLING WITH UNPROTECTED AMINES -- COUPLING OF ORTHO-SUBSTITUTED ARYL IODIDES AND 2-BROMOPHENYL ACETAMIDES: AN EXCEPTION TO THE ORTHO EFFECT -- SUPPORTING INFORMATION -- GENERAL REMARKS -- COUPLING OF ORTHO-SUBSTITUTED ARYL IODIDES AND BROMOBENZYL AMINES -- COUPLING OF ORTHO-SUBSTITUTED ARYL IODIDES AND 2-BROMOPHENYL ACETAMIDES.In this dissertation, Marie-Hélène Larraufie develops original radical and pallado-catalyzed methodologies to enable the synthesis of several classes of bioactive nitrogen-containing heterocycles. New radical cascades employing the N-acylcyanamide moiety offer straightforward routes to quinazolinones and guanidines, as well as new insights into the mechanism of homolytic aromatic substitutions. In parallel, Larraufie expands the scope of visible light photoredox catalysis to the ring opening of epoxides and aziridines, thus providing new sustainable alternatives for the generation of radicals. Furthermore, in a collaborative effort with the Catellani group, the author investigates dual palladium/norbornene catalysis. First, she develops a C-amination coupling variant of the Catellani reaction with unprotected amines which provides an expeditious route to phenanthridines. Then, she examines the influence of the chelating effect on Pd(IV) intermediates reactivity with the help of experimental studies and DFT calculations. The work in this thesis has resulted in numerous publications in high impact journals.The clarity and depth of the experimental section will be useful for students and researchers working in this field. .Springer theses.Heterocyclic compoundsCalcium cyanamideQuinazolineGuanidineHeterocyclic compounds.Calcium cyanamide.Quinazoline.Guanidine.547.590459Larraufie Marie-Heleneauthttp://id.loc.gov/vocabulary/relators/aut1063577MiFhGGMiFhGGBOOK9910298659303321Development of New Radical Cascades and Multi-Component Reactions2533026UNINA