00737nam0-2200265 --450 991027996040332120180717093159.0(OCoLC)1211546320180717d1967----km y0itay50 ----bafreFRDemain, le chemin de fer ..par Henri LartilleuxParisSociété d'édition d'enseignement supérieur1967267 pill.18 cmDemain?Ferrovia385Lartilleux,Henri<1904- >139006ITUNINARICAUNIMARCBK9910279960403321G1/1131264DINTRDINTRDemain, le chemin de fer .1510321UNINA02191nam 22004693u 450 991083021340332120230801222630.03-527-66123-93-527-66121-21-280-66302-297866136399503-527-66124-7(CKB)2670000000179104(EBL)896370(OCoLC)792685091(MiAaPQ)EBC896370(MiAaPQ)EBC4044437(EXLCZ)99267000000017910420130418d2012|||| u|| |gerur|n|---|||||Patente, Marken, Design von A bis Z[electronic resource]Weinheim Wiley20121 online resource (433 p.)Description based upon print version of record.3-527-32371-6 Title Page; Inhaltsverzeichnis; Vorwort; Benutzungshinweise; Lexikalischer Teil; Fachwortverzeichnisse; Deutsch - Englisch - Französisch; Englisch - Deutsch - Französisch; Französisch - Deutsch - EnglischPatentrecht, Markenrecht und Designschutz bilden einen Bereich, der ständigem Wandel unterworfen ist. Selbst für Spezialisten ist es zur Herausforderung geworden, Rechte und Forschungsergebnisse zu schützen in einem internationalen Umfeld, das täglich komplexer wird. Basierend auf dem 1991 erschienenen erfolgreichen Werk ""Patentbegriffe von A bis Z"" und ergänzt um ein dreisprachiges Fachwortverzeichnis, führt das hoch vernetzte Glossar durch den Dschungel der Begrifflichkeiten und berücksichtigt dabei alle aktuellen rechtlichen Änderungen wie: einheitliche Marken für die EU, Auswirkung vIndustrial property (International law)International business enterprises - MexicoIndustrial property (International law).International business enterprises - Mexico.332 673346.048603Münch Volker989485AU-PeELAU-PeELAU-PeELBOOK9910830213403321Patente, Marken, Design von A bis Z4032788UNINA05480nam 2200721Ia 450 991101944220332120200520144314.09786610854202978128085420012808542009783527607549352760754497835276071293527607129(CKB)1000000000376400(EBL)481674(SSID)ssj0000175535(PQKBManifestationID)11156097(PQKBTitleCode)TC0000175535(PQKBWorkID)10204132(PQKB)11608884(MiAaPQ)EBC481674(OCoLC)85821165(Perlego)2769522(EXLCZ)99100000000037640020050519d2006 uy 0engur|n|---|||||txtccrHydrolases in organic synthesis regio- and stereoselective biotransformations /Uwe T. Bornscheuer and Romas J. Kazlauskas2nd ed.Weinheim Wiley-VCH ;Chichester John Wileyc20061 online resource (369 p.)Description based upon print version of record.9783527310296 3527310290 Includes bibliographical references and index.Hydrolases in Organic Synthesis; Preface for the 2(nd) edition; Preface for the 1(st) edition; Acknowledgments; Contents; 1 Introduction; 2 Designing Enantioselective Reactions; 2.1 Kinetic Resolutions; 2.1.1 Recycling and Sequential Kinetic Resolutions; 2.1.2 Dynamic Kinetic Resolutions; 2.1.2.1 Introduction; 2.1.2.2 Racemization by Protonation/Deprotonation; 2.1.2.3 Racemization by Addition/Elimination; 2.1.2.4 Racemization by Nucleophilic Substitution; 2.1.2.5 Racemization by Oxidation/Reduction; 2.1.2.6 Related Strategies; 2.2 Asymmetric Syntheses3 Choosing Reaction Media: Water and Organic Solvents3.1 Hydrolysis in Water; 3.2 Transesterifications and Condensations in Organic Solvents; 3.2.1 Increasing the Catalytic Activity in Organic Solvents; 3.2.1.1 Choosing the Best Organic Solvent for High Activity; 3.2.2 Increasing the Enantioselectivity in Organic Solvents; 3.2.3 Water Content and Water Activity; 3.3 Other Reaction Media; 3.3.1 Ionic Liquids; 3.3.2 Reverse Micelles; 3.3.3 Supercritical Fluids; 3.4 Immobilization; 3.4.1 Introduction; 3.4.1.1 Increasing the Surface Area to Increase Catalytic Activity4 Protein Sources and Optimization of Biocatalyst Performance4.1 Accessing Biodiversity; 4.2 Creating Improved Biocatalysts; 4.2.1 Directed Evolution; 4.2.1.1 Methods to Create Mutant Libraries; 4.2.1.2 Assay Systems; 4.2.1.3 Selected Examples; 4.2.2 Focused Directed Evolution; 4.3 Catalytic Promiscuity in Hydrolases; 4.3.1 Reactions Involving Functional Group Analogs; 4.3.1.1 Perhydrolases; 4.3.2 Aldol and Michael additions Catalyzed by Hydrolases; 4.3.2.1 Aldol Additions; 4.3.2.2 Michael-Type Additions; 4.3.3 Modifications to Introduce New Reactivity in Hydrolases4.3.3.1 Enantioselective Reduction of Hydroperoxides with Selenosubtilisin4.3.3.2 Vanadate-Modified Phosphatases as Peroxidases; 5 Lipases and Esterases; 5.1 Availability, Structures and Properties; 5.1.1 Lipases; 5.1.1.1 Classification of Lipases; 5.1.1.2 General Features of PPL, PCL, CRL, CAL-B, and RML; 5.1.2 Esterases; 5.1.3 Lipases and Esterases are α/β Hydrolases; 5.1.4 Lid or Flap in Interfacial Activation of Lipases; 5.1.5 Substrate Binding Site in Lipases and Esterases; 5.1.6 Designing Reactions with Lipases and Esterases; 5.1.6.1 Acyl Donor for Acylation Reactions5.1.7 Assays for Lipases and Esterases5.1.7.1 Requirements for a Suitable Assay; 5.1.7.2 How to Distinguish Between Lipase, Esterase, and Protease; 5.2 Survey of Enantioselective Lipase-Catalyzed Reactions; 5.2.1 Alcohols; 5.2.1.1 Secondary Alcohols; 5.2.1.2 Primary Alcohols; 5.2.1.3 Other Alcohols, Amines, and Alcohol Analogs; 5.2.2 Carboxylic Acids; 5.2.2.1 General Considerations; 5.2.2.2 Carboxylic Acids with a Stereocenter at the α-Position; 5.2.2.3 Carboxylic Acids with a Stereocenter at the β-Position; 5.2.2.4 Other Carboxylic Acids; 5.2.2.5 Double Enantioselection; 5.2.2.6 Anhydrides5.2.3 LactonesFrom reviews to the first edtion:""Bornscheuer and Kazlauskas have set out, and succeeded, in producing a definitive manual on hydrolytic enzymes (especially lipases, esterases, and proteases) for organic chemists. This is quite simply the best book of its type and can be unreservedly recommended to organic chemists who have an interest in using hydrolytic enzymes in synthesis."" (Nicholas J. Turner, University of Edinburgh)""The book is an indispensable source of information on the use of hydrolases in organic synthesis. The subject matter is very well set out, and the chapterCatalysisHydrolasesOrganic compoundsSynthesisCatalysis.Hydrolases.Organic compoundsSynthesis.547.235.74bclBornscheuer U. T(Uwe Theo),1964-1839804Kazlauskas R. J(Romas J.),1956-886693MiAaPQMiAaPQMiAaPQBOOK9911019442203321Hydrolases in organic synthesis4419173UNINA00870nam0-2200265 --450 991102137420332120250905122700.020250905d1884----kmuy0itay5050 baitaIT 001yyDizionario dei sinonimi della lingua italianaper cura di Niccolò Tommaseo7. ed. milanese fatta sulla 5.accresciuta e rifusa in nuovo ordine dall'autoreed. stereotipa ricorrettaMilanoF. Vallardi1884LXIV, 1222 p.26 cm.SinonimiDizionari453.1223itaTommaseo,Niccolò337187ITUNINAREICATUNIMARCBK9911021374203321A MUSA 89303/4095/25FAGBCFAGBCDizionario dei sinonimi della lingua italiana147221UNINA04241nam 2200589Ia 450 991096028030332120251117092514.01-61487-766-1(CKB)2670000000276653(EBL)3327328(SSID)ssj0000756792(PQKBManifestationID)11390427(PQKBTitleCode)TC0000756792(PQKBWorkID)10753390(PQKB)11333432(OCoLC)654641993(MdBmJHUP)muse24468(Au-PeEL)EBL3327328(CaPaEBR)ebr10623044(CaONFJC)MIL587790(OCoLC)929118671(MiAaPQ)EBC3327328(BIP)42484654(BIP)6036228(EXLCZ)99267000000027665319990825d2000 uy 0engur|n|---|||||txtccrThe revolutionary writings of John Adams /selected and with a foreword by C. Bradley ThompsonIndianapolis Liberty Fund20001 online resource (353 p.)Description based upon print version of record.0-86597-285-0 Includes bibliographical references and index.""John Adams, The Revolutionary Writings Of ""; ""Front Matter ""; ""Title Page ""; ""Publishing Details ""; ""Table of Contents, p. vii ""; ""Foreword, p. ix ""; ""Acknowledgments, p. xvii ""; ""Editor's Note, p. xviii ""; ""The Revolutionary Writings of John Adams ""; ""Essays and Controversial Papers of the Revolution, p. 1 ""; ""A Dissertation on the Canon and Feudal Law, p. 19 ""; ""Instructions of the Town of Braintree to Their Representative, p. 37 ""; ""The Earl of Clarendon to William Pym, p. 43 ""; ""Governor Winthrop to Governor Bradford, p. 57 """"The Independence of the Judiciary, p. 73 """"Two Replies of the Massachusetts House of Representatives to Governor Hutchinson, p. 117 ""; ""Novanglus; or, A History of the Dispute with America, p. 147 ""; ""Thoughts on Government, p. 285 ""; ""The Report of a Constitution, or Form of Government, for the Commonwealth of Massachusetts, p. 295 ""; ""Index, p. 323 """Conservatives who are gratified at the success of David McCullough's wonderful new biography of John Adams will find even more of the real Adams--Adams unplugged, one might say in""The Revolutionary Writings of John Adams."--"Michael Potemra, National Review/July 23, 2001""The Revolutionary Writings of John Adams" presents the principal shorter writings in which Adams addresses the prospect of revolution and the form of government proper to the new United States. Though one of the principal framers of the American republic and the successor to Washington as president, John Adams receives remarkably little attention among many students of the early national period. This is especially true in the case of the periods before and after the Revolution, in which the intellectual rationale for independence and republican government was given the fullest expression."The Revolutionary Writings of John Adams" illustrates that it was Adams, for example, who before the Revolution wrote some of the most important documents on the nature of the British Constitution and the meaning of rights, sovereignty, representation, and obligation. And it was Adams who, once the colonies had declared independence, wrote equally important works on possible forms of government in a quest to develop a science of politics for the construction of a constitution for the proposed republic.C. Bradley Thompson is an Associate Professor of History and Political Science at Ashland University, Ashland, Ohio, and the author of "John Adams and the Spirit of Liberty."United StatesPolitics and government1775-1783MassachusettsPolitics and government1775-1783973.4/4/092Adams John1735-1826.287392Thompson C. Bradley1872534MiAaPQMiAaPQMiAaPQBOOK9910960280303321The revolutionary writings of John Adams4481727UNINA