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  • 1
    Online Resource
    Online Resource
    La Vergne :RSC,
    Keywords: Electronic books.
    Description / Table of Contents: Reflecting the growing volume of published work in this field, researchers will find this book an invaluable source of information on current methods and applications.
    Type of Medium: Online Resource
    Pages: 1 online resource (618 pages)
    Edition: 1st ed.
    ISBN: 9781847556288
    Series Statement: ISSN Series
    Language: English
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  • 2
    Online Resource
    Online Resource
    La Vergne :Royal Society of Chemistry, The,
    Keywords: Organic compounds -- Synthesis. ; Electronic books.
    Description / Table of Contents: Reflecting the growing volume of published work in this field, researchers will find this book an invaluable source of information on current methods and applications.
    Type of Medium: Online Resource
    Pages: 1 online resource (618 pages)
    Edition: 1st ed.
    ISBN: 9781847556288
    Series Statement: Issn Series
    DDC: 547
    Language: English
    Note: General and Synthetic Methods -- Contents -- Chapter 1 Saturated and Unsaturated Hydrocarbons -- 1 Saturated Hydrocarbons -- 2 Olefinic Hydrocarbons -- 3 Stereoselective, Simultaneous Formation of sp3 and sp2 Centres -- Claisen Rearrangements -- [2,3] Wittig Rearrangements -- 4 Conjugated Dienes -- 5 Non-conjugated Dienes -- 6 Polyenes -- 7 Allenes -- 8 Alkynes -- 9 Enynes -- References -- Chapter 2 Aldehydes and Ketones -- 1 Synthesis of Aldehydes and Ketones -- Oxidative Methods -- Reductive Methods -- Methods Involving Umpolung -- Other Methods -- Cyclic Ketones -- 2 Synthesis of Functionalised Aldehydes and Ketones -- Unsaturated Aldehydes and Ketones -- α-Substituted Aldehydes and Ketones -- Dicarbonyl Compounds -- 3 Protection and Deprotection of Aldehydes and Ketones -- 4 Reactions of Aldehydes and Ketones -- Reactions of Enolates -- Aldol Reactions -- Conjugate Addition Reactions -- References -- Chapter 3 Carboxylic Acids and Derivatives -- 1 Carboxylic Acids -- General Synthesis -- Diacids -- Hydroxy-acids -- Keto-acids -- Unsaturated Acids -- Aromatic Acids -- Halo-acids -- Carboxylic Acid Protection -- 2 Carboxylic Acid Esters -- Esterification -- General Synthesis -- Diesters -- Hydroxy-esters -- Keto-esters -- Unsaturated Esters -- Halo-esters -- Thioesters -- 3 Carboxylic Acid Amides -- General Synthesis -- Hydroxy-amides -- Keto-amides -- Unsaturated Amides -- Thioamides -- 4 Lactones -- General Synthesis -- Butyrolactones -- α-Methylene- and α-Alkylidenebutyrolactones -- γ-Alkylidinebutyrolactones -- Butenolides -- Tetronic Acids -- Phthalides -- Valerolactones -- Macrolides -- 5 Amino Acids -- α-Amino acids -- Dehydroamino acids -- Hydroxy α-amino acids -- β-Amino acids -- Amino-acid Coupling -- Amino-acid Protection -- References -- Chapter 4 Alcohols, Halogeno Compounds, and Ethers -- 1 Alcohols -- Preparation. , By Addition to Olefins -- By Reduction of Carbonyl Compounds -- By Nucleophilic Alkylation -- Non Stereoselective Addition -- Selective Addition -- By Opening of Epoxides -- Miscellaneous Methods -- Protection and Deprotection -- Oxidation and Deoxygenation -- 2 Halogeno Compounds -- 3 Ethers and Thioethers -- References -- Chapter 5 Amines, Nitriles, and Other Nitrogen-containing Functional Groups -- 1 Amines -- Acyclic Amines -- Aromatic Amines -- Allylic Amines -- Cyclic Amines -- Protecting Groups -- Enamines -- Alkyldiamines -- 2 Amino-alcohols -- 1,2-Amino-alcohols -- 1,3-Amino-alcohols -- 1,2-Amino-thiols, 1,2-Aminoketones, and α-Aminophosphonic Acids -- Azo Compounds -- Nitriles -- Nitro Compounds -- Nitroxyl and Nitroso Compounds -- Alkyl Nitrates and Nitramines -- Hydroxylamines -- Imines -- Amidines -- Oximes and Hydrazones -- Thiodiimides -- Azides -- Thiocyanates, Isothiocyanates, and Isocyanides -- References -- Chapter 6 Organometallics in Synthesis -- Part I: The Transition Elements -- 1 Introduction -- 2 Reduction -- 3 Oxidation -- 4 Isomerisations and Rearrangements -- 5 Carbon-Carbon Bond-Forming Reactions -- Via Organometallic Electrophiles -- Via Organometallic Nucleophiles -- Via Coupling and Cycloaddition Reactions -- Via Carbonylation Reactions -- 6 Miscellaneous Reactions -- References -- Part II: Main Group Elements -- 1 Group I -- Lithium Amides -- Lithium Enolates -- Non-stabilized Organolithium Reagents -- Lithiated Aromatic and Heteroaromatic Rings -- Benzylic and Allylic Lithium Anions -- Alkenyl and Alkynyl Lithium Anions -- Di- and Trilithiated Anions -- Sodium and Potassium -- Anions Stabilised by Sulphur, Silicon, and Selenium -- 2 Group II -- Magnesium -- Zinc and Mercury -- 3 Group III -- Boron -- Aluminium and Thallium -- 4 Group IV -- Silicon and Germanium. , Allyl, Benzyl, and Alkenyl Silanes and their Derivatives -- Tin and Lead -- 5 Group V -- Phosphorus -- Arsenic, Antimony, and Bismuth -- 6 Group VI -- Sulphur -- Selenium and Tellurium -- References -- Chapter 7 Saturated Carbocyclic Ring Synthesis -- 1 Three-membered Rings -- 2 Four-membered Rings -- 3 Five-membered Rings -- Transition Metal Mediated Cyclisations -- Radical Cyclisations -- Other Routes to Five-membered Rings -- 4 Six-membered Rings -- Diels-Alder Reactions -- Other Routes to Six-membered Rings -- 5 Seven-membered, Medium, and Large Rings -- Seven and Eight-membered Rings -- Large Rings -- Ring Expansions -- References -- Chapter 8 Saturated Heterocyclic Ring Synthesis -- 1 Oxygen-containing Heterocycles -- Three-membered Rings -- Four-membered Rings -- Five-membered Rings -- Tetrahydrofurans -- Dihydrofurans and Benzofurans -- Five-membered Rings with More than One Oxygen -- Six-membered Rings -- Tetrahydropyrans -- Dihydropyrans -- Six-membered Rings with More than One Oxygen -- Medium- and Large-ring Ethers -- 2 Sulphur-containing Heterocycles -- 3 Heterocycles Containing More than One Heteroatom -- Nitrogen- and Oxygen-containing Rings -- Five-membered Rings -- Six- and Seven-membered Rings -- Nitrogen- and Sulphur, and Sulphur- and Oxygen- containing Rings -- 4 Nitrogen-containing Heterocycles -- Three- and Four-membered Rings -- Five-membered Rings -- Six-membered Rings Containing One Nitrogen -- Five- and Six-membered Rings with Two Nitrogen Atoms -- Seven-membered and Larger Rings -- β-Lactam -- References -- Chapter 9 Highlights in the Total Synthesis of Natural Products -- 1 Terpenes -- 2 Alkaloids -- 3 Spiroacetals -- 4 Macrolides -- 5 Polyether Antibiotics -- 6 Tetronolides -- 7 Enediynes -- 8 Other Natural Products -- References -- Chapter 10 Reviews on General and Synthetic Methods. , 1 Saturated and Unsaturated Hydrocarbons -- 2 Halogeno Compounds -- 3 Sulphur Compounds -- 4 Carbonyl Compounds -- 5 Carboxylic Acids and Derivatives -- 6 Carbocyclic Ring Synthesis -- 7 Heterocyclic Ring Synthesis and Alkaloids -- 8 Organometallics -- 9 Asymmetric Synthesis and Stereoselective Processes -- 10 Natural Products Synthesis -- 11 Nucleosides -- 12 Radicals in Synthesis -- 13 Carbohydrates -- 14 Cycloaddition Reactions -- 15 Pressure Reactions -- 16 Photochemistry and Electrochemistry -- 17 General -- Author Index.
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 110 (1988), S. 1307-1308 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 111 (1989), S. 8314-8315 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 57 (2001), S. o796-o797 
    ISSN: 1600-5368
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The title compound, C8H16N2O4, is the product of a Mitsunobu coupling using the diisopropylazodicarboxylate. It forms hydrogen-bonded chains similar to those in its previously reported diethyl analogue.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 56 (2000), S. e224-e226 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Compounds (I), C14H20N2O4S, and (II), C12H14N2O3S2, are two minor products of the same reaction. Both structures contain identical ester functionalities in similar orientations. Both independent molecules of (I) contain an ethoxycarbothioylamine moiety, whilst (II) possesses a novel exocyclic thione system fused with a pyridine ring.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 56 (2000), S. 687-688 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The title compound, C11H8N4S, is found to have a symmetrical resonance structure in which both pyridyl-N atoms interact with the S atom forming hemi-bonds. This also results in the formation of a delocalized diimine region and disturbance of the aromaticity in the pyridyl rings.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 28 (1993), S. 478-480 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0044-8249
    Keywords: Atropisomerie ; Isomerisierungen ; Makrocyclen ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 0570-0833
    Keywords: atropisomerism ; isomerizations ; macrocycles ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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