02008nam 2200373 n 450 99639225310331620200824121655.0(CKB)4940000000109222(EEBO)2240902196(UnM)99864711e(UnM)99864711(EXLCZ)99494000000010922219931208d1648 uy |engurbn||||a|bb|The declaration of Duke Hambleton at the head of his army[electronic resource] upon his joyning with Maj. Gen. Langdale in the north of England, concerning His most Gracious and Dread Soveraign Charkes [sic] King of Great Brittain. Likewise Major Generall Langdales propositions to the Lord Duke, concerning the Kings Majesty, and the Dukes answer thereunto. And the resolution of the Scots Army, with the manner of their march, their trumpets sounding, drums beating, and collours displaying with this motto, For Religion, King and Kingdom. Also the Duke of Buckinghams representation to the Lord Major of London, and his declaration, concerning the Kings Majesty[London] Printed for the generall satisfaction of all true subjects1648[2], 6 pPlace of publication from Wing.In fact only three letters, one signed on p.5: A.H. (i.e. James Hamilton), and two signed on p.6: G. Buckingham (i.e. George Villiers Buckingham).Annotation on Thomason copy: "July 9th".Reproduction of the original in the British Library.eebo-0018Great BritainHistoryCivil War, 1642 1649Early works to 1800Hamilton James HamiltonDuke of,1606-1649.1005102Buckingham George VilliersDuke of,1628-1687.793404Cu-RivESCu-RivESCStRLINWaOLNBOOK996392253103316The declaration of Duke Hambleton at the head of his army2354996UNISA04332 am 2200997 n 450 9910516006003321202112162-37154-156-710.4000/books.iheal.9362(CKB)4100000012293618(FrMaCLE)OB-iheal-9362(oapen)https://directory.doabooks.org/handle/20.500.12854/85469(PPN)259402613(EXLCZ)99410000001229361820211214j|||||||| ||| 0freuu||||||m||||txtrdacontentcrdamediacrrdacarrierLa Pachamama en bases de données Géographie politique de l’information environnementale contemporaine /Pierre GautreauParis Éditions de l’IHEAL20211 online resource (364 p.) Travaux et mémoires2-37154-155-9 Qu’on le déplore ou non, notre rapport au monde biophysique est désormais fermement médiatisé par la mesure et les données numériques. Véritable Janus, cette information dite « environnementale » nous contraint autant qu’elle nous libère et fait l’objet de controverses brûlantes. Vecteur de démocratisation là où elle permet aux populations de connaître les risques qui les concernent et de participer aux décisions environnementales, elle s’avère dangereuse lorsqu’elle renforce des situations de domination sociale, ou appauvrissante quand elle réduit notre compréhension du monde vivant à quelques variables chiffrées. Incapable de représenter la complexité de ce vivant et du rapport que tissent avec lui les humains, elle connecte autant qu’elle marginalise les êtres et les choses. Les enquêtes sud-américaines de cet ouvrage explorent ce que le numérique change aux façons contemporaines d’appréhender les problèmes environnementaux, à travers des récits qui racontent plusieurs tentatives de « mise en bases de données » de la nature au XXIe siècle. De la Pachamama andine au symbole global amazonien, des luttes populaires pour le droit à l’information aux velléités de régulation à distance de l’agrobusiness, des controverses sur la standardisation de nos rapports au vivant aux quêtes de souveraineté informationnelle, c’est à un bilan politique nuancé et complexe que le lecteur est convié.Environmental StudiesGeographyAmérique latineArgentineBolivieBrésilUruguaygéographie politiqueinformation environnementalejustice informationnelleécologie politiqueArgentinaBoliviaBrasilgeografía políticaecología políticainformación medioambientaljusticia informacionalBrazilpolitical geographypolitical ecologyenvironmental informationinformational justiceBrazilBoliviaArgentinaUruguaypolitical geographypolitical ecologyenvironmental informationinformational justiceEnvironmental StudiesGeographyAmérique latineArgentineBolivieBrésilUruguaygéographie politiqueinformation environnementalejustice informationnelleécologie politiqueArgentinaBoliviaBrasilgeografía políticaecología políticainformación medioambientaljusticia informacionalBrazilpolitical geographypolitical ecologyenvironmental informationinformational justiceGautreau Pierre1287588FR-FrMaCLEBOOK9910516006003321La Pachamama en bases de données3041007UNINA05553nam 2200673 450 991082834760332120200520144314.01-118-77820-01-118-77817-01-118-77818-9(CKB)2550000001171807(EBL)1582380(SSID)ssj0001082031(PQKBManifestationID)11591791(PQKBTitleCode)TC0001082031(PQKBWorkID)11091741(PQKB)11043443(OCoLC)853618742(MiAaPQ)EBC1582380(DLC) 2013029045(Au-PeEL)EBL1582380(CaPaEBR)ebr10822347(CaONFJC)MIL553207(OCoLC)866449058(PPN)219882622(EXLCZ)99255000000117180720130709d2014 uy 0engur|n|---|||||txtccrMethods and applications of cycloaddition reactions in organic syntheses /edited by Nagatoshi NishiwakiHoboken, New Jersey :Wiley,2014.1 online resource (673 p.)Description based upon print version of record.1-118-29988-4 1-306-21956-6 Includes bibliographical references and index.Methods and Applications of Cycloaddition Reactions in Organic Syntheses; Contents; Preface; Contributors; Part I: [2+1] Cycloaddition; 1 [2+1]-Type Cyclopropanation Reactions; 1.1 INTRODUCTION; 1.2 CYCLOPROPANATION REACTION VIA MICHAEL-INDUCED RING CLOSURE REACTION; 1.2.1 Introduction; 1.2.2 Halo-Substituted Nucleophiles in MIRC Reaction; 1.2.3 Ylides for Cyclopropanation; 1.3 SIMMONS-SMITH CYCLOPROPANATION AND RELATED REACTIONS; 1.3.1 Introduction; 1.3.2 The Simmons-Smith Reaction with Zinc Reagents; 1.4 DIAZOALKANES WITH TRANSITION METAL CATALYSTS; 1.4.1 Introduction1.4.2 Rhodium-Catalyzed Reactions1.4.4 Ruthenium-Catalyzed Reactions; 1.4.5 Cobalt- and Iron-Catalyzed Reactions; 1.4.6 Other Transition Metal-Catalyzed Reactions; 1.4.7 Cyclopropanation Without Transition Metal Catalysts; 1.4.8 Cyclopropanation of Dihalocarbenes; 1.5 CYCLOISOMERIZATION WITH TRANSITION METAL CATALYSTS; 1.5.1 Introduction; 1.5.2 Gold Complex-Catalyzed Reactions; 1.5.3 Palladium Complex-Catalyzed Reactions; 1.5.4 Platinum Complex-Catalyzed Reactions; 1.5.5 Ruthenium Complex-Catalyzed Reactions; 1.5.6 Other Metal Complex-Catalyzed Reactions; 1.6 KULINKOVICH REACTIONS1.6.1 Introduction1.6.2 The Kulinkovich Reaction to Esters, Ketones, and Amides; 1.6.3 Kulinkovich Reaction to Nitriles; 1.6.4 Other Ti-Mediated Cyclopropanation Reactions; 1.7 MISCELLANEOUS [2+1]-TYPE OF CYCLOPROPANATION REACTIONS; REFERENCES; 2 N1 Unit Transfer Reaction To C-C Double Bonds; 2.1 INTRODUCTION; 2.2 AZIRIDINATION WITH AZIDES; 2.3 AZIRIDINATION WITH IMINOIODINANES; 2.4 AZIRIDINATION WITH N-HALOAMINE SALTS; 2.5 AZIRIDINATION WITH OTHER N1 UNIT; 2.6 CONCLUSIONS; REFERENCES; Part II: [2+2] Cycloaddition; 3 Lewis Base Catalyzed Asymmetric Formal [2+2] Cycloadditions3.1 INTRODUCTION3.2 β-LACTAMS: FORMAL [2+2] CYCLOADDITIONS INVOLVING IMINES; 3.3 β-LACTONES I: FORMAL [2+2] CYCLOADDITIONS INVOLVING ALDEHYDES/KETONES; 3.4 β-LACTONES II: FORMAL [2+2] CYCLOADDITION OF KETENES LEADING TO KETENE DIMERS; 3.4.1 Introduction or or; 3.4.2 Homodimerization; 3.4.3 Heterodimerization; 3.5 MISCELLANEOUS FORMAL [2+2] ASYMMETRIC CYCLOADDITION PROCESSES; 3.5.1 Other Heterocyclic Classes-Introduction; 3.5.2 Asymmetric Formal [2+2] Cycloadditions; 3.6 CONCLUSIONS; REFERENCES; Part III: [2+2] and [4+2]/[2+2] Cycloaddition; 4 Catalytic [2+2] Cycloaddition of Silyl Enol Ethers4.1 INTRODUCTION4.2 CATALYTIC [2+2] CYCLOADDITION REACTIONS OF SILYL ENOL ETHERS BY LEWIS ACID CATALYST; 4.2.1 Introduction; 4.2.2 Intramolecular [2+2] Cycloaddition Reactions; 4.2.3 Intermolecular [2+2] Cycloaddition Reactions; 4.2.4 Asymmetric Catalytic [2+2] Cycloaddition Reaction with Silyl Enol Ethers; 4.3 CATALYTIC [2+2] CYCLOADDITION REACTIONS OF SILYL ENOL ETHERS BY BRØNSTED ACID; 4.3.1 Catalytic [2+2] Cycloaddition Reactions of Silyl Enol Ethers by Trifluoromethanesulfonimide; 4.3.2 Multigram Syntheses of Cyclobutanes and Cyclobutenes by [2+2] Cycloaddition Reactions4.3.3 Analysis of the Mechanism for [2+2] Cycloaddition Reactions by TrifluoromethanesulfonimideAlthough these reactions have been studied for a long time, cycloaddition chemistry makes frequent and considerable advances that requires chemists to keep constantly up-to-date with the practices and state-of-the-art. Bringing together the contributions from leading worldwide researchers, Methods and Applications of Cycloaddition Reactions in Organic Syntheses provides a valuable guidebook for synthetic organic chemists involved in chemical research, pharmaceuticals, and materials science to keep organic chemists updated and current in the practices of cycloadditions, a leading class oOrganic compoundsSynthesisRing formation (Chemistry)Organic compoundsSynthesis.Ring formation (Chemistry)547/.27Nishiwaki Nagatoshi1963-1294155MiAaPQMiAaPQMiAaPQBOOK9910828347603321Methods and applications of cycloaddition reactions in organic syntheses4017860UNINA