01040nam0-2200301---450-99000837652040332120060914112349.0000837652FED01000837652(Aleph)000837652FED0100083765220060914d1989----km-y0itay50------bagerDEa-------001yyRasterorientierte Informationssysteme in der GeographieKonzepte und Erfahrungen bei der Realisierung eines GIS für die WaldschadenforschungHelmut SaurerWurzburgSelbstverlag des Instituts für Geographie der Univ1989viii, 114 p.ill.21 cmWürzburger geographische Arbeiten74GeografiaSistemi informativiSaurer,Helmut274161ITUNINARICAUNIMARCBK990008376520403321Period.026(074)Ist. s.i.ILFGEILFGERasterorientierte Informationssysteme in der Geographie723335UNINA05265nam 2200649 a 450 991045779010332120200520144314.01-283-34773-397866133477320-08-096631-4(CKB)2550000000074522(EBL)829958(SSID)ssj0000592324(PQKBManifestationID)12244226(PQKBTitleCode)TC0000592324(PQKBWorkID)10736184(PQKB)11411100(MiAaPQ)EBC829958(PPN)182571424(Au-PeEL)EBL829958(CaPaEBR)ebr10518436(CaONFJC)MIL334773(OCoLC)769344338(EXLCZ)99255000000007452220111221d2012 uy 0engur|n|---|||||txtccrOrganic syntheses based on name reactions[electronic resource] a practical guide to over 750 transformations /A. Hassner, I. Namboothiri3rd ed.Oxford Elsevier20121 online resource (612 p.)Includes indexes.0-08-096630-6 Front Cover; Organic Syntheses Basedon Name Reactions: A Practical Guide to 750 Transformations; Copyright; Contents; Foreword by D. Seebach; Foreword by S. Danishefsky; Preface to the Third Edition; Preface to the Second Edition; Preface to the First Edition; An Overview of Synthesis Related Name Reactions; Overview - Pd Catalyzed C-C Coupling Name Reactions; List of Abbreviations; ABIKO-MASAMUNE Asymmetric Aldol Reaction; ABRAMOV Asymmetric Phosphonylation; ACHMATOWICZ Furanylcarbinol Rearrangement; ACYLOIN Rearrangement; ADLER Phenol Oxidation; ALDER (Ene) ReactionALDER-RICKERT Acetylene CycloadditionALDOL Reactions; ALLEN Phosphonium Rearrangement; ALPER Carbonylation; AMADORI Glucosamine Rearrangement; ANGELI-RIMINI Hydroxamic Acid Synthesis; APPEL Displacement Reagent; ARBUZOV Phosphonate Synthesis; ARNDT-EISTERT RCOOH Homologation; ASINGER Thiazoline Synthesis; ATHERTON-TODD Phosphoramidate Synthesis; AUWERS Flavone Synthesis; AUWERS-INHOFFEN Dienone-Phenol Rearrangement; BAER-FISCHER Amino Sugar Synthesis; BAEYER Pyridine Synthesis; BAEYER Diarylmethane Synthesis; BAEYER-DREWSON Indoxyl Synthesis; BAEYER Oxindole SynthesisBAEYER-VILLIGER Aromatic TritylationBAEYER-VILLIGER Ketone Oxidation; BAILEY Crisscross Cycloaddition; BAKER-VENKATARAMAN Flavone Synthesis; BALABAN Pyrylium Salt Synthesis; BALLY-SCHOLL Benzanthrene Synthesis; BALSON Aromatic Alkylation; BAMBERGER Benzotriazine Synthesis; BAMBERGER Imidazole Cleavage; BAMFORD-STEVENS Tosylhydrazone Decomposition; BARBAS-LIST Asymmetric Michael Reaction; BARBIER In Situ Grignard Reaction; BARBIER-WIELAND Ester Chain Degradation; BARDHAN-SENGUPTA Phenanthrene Synthesis; BARGELLINI 3-Component Carboxylic Acid Synthesis; BARLUENGA Iodination ReagentBARTON ArylationBARTON Deamination; BARTON Decarboxylation; BARTON Nitrite Photolysis; BARTON-KELLOG Olefination; BARTON-McCOMBIE Alcohol Deoxygenation; BART-SCHELLER Aromatic Arsonylation; BAUDISCH Nitrosophenol Synthesis; BECHAMP Phenol, Aniline Arsonilation; BECKMANN Oxime Rearrangement or Fragmentation; BELLER Multicomponent Amino Acid Synthesis; BENARY Conjugated Aldehyde Synthesis; BERCHTOLD Enamine Homologation; BERGMAN Cycloaromatization; BERNTHSEN Acridine Synthesis; BERTRAND-STEPHAN Metal-free Bond Activation; BESTMANN Cumulene Ylides; BIGINELLI Pyrimidone SynthesisBIRCH Na-NH3 ReductionBISCHLER Benzotriazine Synthesis; BISCHLER-MOHLAU Indole Synthesis; BISCHLER-NAPIERALSKI Isoquinoline Synthesis; BLACK Enol Carbonate Rearrangement; BLANC-QUELLET Chloroalkylation; BLICKE-PACHTER Pteridines Synthesis; BLOMQUIST Macrocycles Synthesis; BLUM Aziridine Synthesis; BODROUX-CHICHIBABIN Aromatic Aldehyde Synthesis; BOEKELHEIDE Dipole Ring Expansions; BOGER Thermal Cycloadditions; BOGER N-Heterocycles by Reverse Demand Diels-Alder; BOORD Enol Ether Synthesis; BORCH Reductive Amination; BORSCHE-BEECH Aromatic Aldehyde SynthesisBOULTON-KATRITZKY Heterocyclic RearrangementOrganic Syntheses Based on Named Reactions is an indispensable reference companion for chemistry students and researchers. Building on Hassner & Stumer's highly regarded 2e, this new work reviews 750 reactions, with over 100 new stereoselective and regioselective reactions. Each A-Z entry provides a carefully condensed summary of valuable information that a chemist needs to understand and utilize these fundamental reactions in their work, including brief practical details. The book is illustrated with real synthetic examples from the literature and about 3,400 references to the primaOrganic compoundsSynthesisElectronic books.Organic compoundsSynthesis.547.2547/.2Hassner Alfred92785Namboothiri I1034707MiAaPQMiAaPQMiAaPQBOOK9910457790103321Organic syntheses based on name reactions2454002UNINA01963nam 2200601Ia 450 991045077980332120200520144314.00-7914-8693-11-4175-3876-7(CKB)1000000000447474(OCoLC)56418461(CaPaEBR)ebrary10594737(SSID)ssj0000239422(PQKBManifestationID)11195062(PQKBTitleCode)TC0000239422(PQKBWorkID)10239930(PQKB)10143296(MiAaPQ)EBC3408410(MdBmJHUP)muse6001(Au-PeEL)EBL3408410(CaPaEBR)ebr10594737(EXLCZ)99100000000044747420021107d2003 ub 0engurcn|||||||||txtccrRomantic science[electronic resource] the literary forms of natural history /Noah Heringman, editorAlbany State University of New York Pressc20031 online resource (297 p.) SUNY series, studies in the long nineteenth centuryBibliographic Level Mode of Issuance: Monograph0-7914-5701-X Includes bibliographical references and index.English literature19th centuryHistory and criticismNature in literatureLiterature and scienceGreat BritainHistory19th centuryNatural history in literatureElectronic books.English literatureHistory and criticism.Nature in literature.Literature and scienceHistoryNatural history in literature.820.9/36Heringman Noah1017541MiAaPQMiAaPQMiAaPQBOOK9910450779803321Romantic science2441956UNINA