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1.

図書

図書
Frederick A. Bettelheim ... [et al.]
出版情報: Boston, MA : Cengage Learning, c2016  1 v. (various pagings) ; 29 cm
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2.

図書

図書
Leroy G. Wade, Jr. ; contributing author, Jan William Simek
出版情報: Harlow : Pearson, c2017  1394 p. ; 28 cm
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3.

図書

図書
Editor : John B. Birks
出版情報: London ; New York : J. Wiley, c1973-c1975  2 v. ; 24 cm
シリーズ名: Wiley monographs in chemical physics
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4.

図書

図書
Stuart J. Baum
出版情報: New York : Macmillan , London : Collier Macmillan, c1987  xv, 526 p. ; 25 cm
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5.

図書

図書
Saad S.M. Hassan
出版情報: Chichester : E. Horwood , New York : Halsted Press, 1984  384 p. ; 24 cm
シリーズ名: Ellis Horwood series in analytical chemistry
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6.

図書

図書
Lawrence J. Andrews and Raymond M. Keefer
出版情報: Amsterdam : Holden-Day, 1964.  196 p. ; 25 cm.
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7.

図書

図書
Ronald Breslow
出版情報: New York : W. A. Benjamin, 1965  xii, 232 p. ; 22 cm
シリーズ名: The Organic chemistry monograph series
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8.

図書

図書
edited by G.R. Desiraju
出版情報: Amsterdam ; Tokyo : Elsevier Science, 1987  xx, 550 p. ; 25 cm
シリーズ名: Studies in organic chemistry ; 32
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9.

図書

図書
by Fritz Feigl in collaboration with Vinzenz Anger ; translated by Ralph E. Oesper
出版情報: Amsterdam ; New York : Elsevier Pub. Co., 1966  xxiii, 772 p. ; 23 cm
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10.

図書

図書
Alexander McKillop
出版情報: New York : Pergamon, 1997  xix, 153 p. ; 25 cm
シリーズ名: Tetrahedron organic chemistry series ; v. 16
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Selected Problems: A tandem route to 1,2,3,4-tetrasubstituted naphthalenes
The Hooker oxidation
Benzopyrene synthesis - by accident
Lactone ammonolysis
Acid-catalysed condensation of indole with acetone
Flash vacuum pyrolysis of o-xylylene dimers
A ""stable enol"" that doesn't exist
Reaction of benzothiazole with DMAD
Ring contractions of a dibenzothiepinone
Rearrangement of 6-hydroxyprotopine to dihydrosanguinarine
An intramolecular Wittig reaction
Easy contruction of a tricyclic indole related to
Selected Problems: A tandem route to 1,2,3,4-tetrasubstituted naphthalenes
The Hooker oxidation
Benzopyrene synthesis - by accident
11.

図書

図書
J. L. Malleron, J. C. Fiaud and J. Y. Legros
出版情報: London : Academic, c1997  304 p. ; 30 cm
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Abbreviations
Introduction
Graphical Abstracts of Reaction Numbers (RXN)
Reactions Catalyzed by Palladium Complexes: Cross-Coupling of Organometallics with RX Derivatives
Cross-Coupling of Organometallicswith RCOX Derivatives
Cross-Coupling of Siloxycyclopropanes with RX and RCOX Derivatives
Cross-Coupling of Terminal Alkynes with RX Derivatives
Intermolecular HECK Reaction
Intramolecular HECK Reaction
Intramolecular Coupling of Di(Vinyl Halides)
Tandem HECK-Anion Capture Process of Alkenes, Alkyenes, Alkynes, Allenes and Dienes
Tandem HECK-Anion Capture Process of Norbonene and Related Compounds
Tandem Arylsulfonation-Cyclization Process
Tandem Cyclization-Anion Capture (-Carbonylation) Processof Alkenes and Alkynes
Tandem Cyclization-Anion Capture (-Carbonylation) Process of Ene-Vinyl, Ene-Aryl, and Ene-Alkyl Halides
Tandem Cyclization-Anion Capture Process of Yne-Vinyl and Yne-Aryl Halides
Hydroarylation and Hydrovinylation of Alkenes andAlkynes
Reduction of Alkenes
Semihydrogenation of Alkynes and 1,3-Dienes
Hydroboration, Hydrogennyladon, Hydrosilylation and Hydrostannation of Alkynes, Allenes, Dienes, and Enynes
Hydroselenation of Alkynes
1,4-Disilyation of Conjugated Enones
Hydrocarboxylation, Hydrocarboalkoxylation and Hydrocarboamination of Alkenes and Alkynes
Tandem Carbonylation-Arylation with Alkynes
1,2-Dimetallation of Alkynes and Alkenes and Related Reactions
1,2-Dimetallation of Isonitriles
1,2-Dimetallation of Allenes
Coupling of Aryl Derivatives with Alkenes Involving a Pd(II) Catalyst
Homocoupling of Aryl and Vinyl Derivatives
Codimerization of Alkynes
Codimerization of Terminal Alkynes with Allenes
Codimerization of Alkynes and Allyl Halides
Cyclopropanation of Alkenes and 1,3-Dienes by Diazomethane
Rearrangement of (-Hydroxy Diazo Compounds
Substitution, Addition, and Elimination on Pro-(-Allyl Substrates
[3,3]-Sigmatropic Rearrangement and [1,3]-Shift on Allylic Derivatives
1,3-Diene Monoepoxide Rearrangement
Ring Extension of Cyclobutane Derivatives
[3+2], [3+4], [3+6], [1+2] Cycloadditions
Intramolecular Ene-Like Reactions
Cyclization of Hexatrienolate Derivatives
Amination or Amidation of Alkenes
Alkoxylation of Alkenes and Alkynes
Acetalization of Alkenes
Allylic Acyloxylation of Cycloalkenes
Tandem Acyloxylation-Cyclization of 1,5-Dienes
Tandem Acycloxychlorination-Cyclization of 1,6-Dienes
1,4-Acycloxychlorination of 1,3-Dienes
1,4-Diacyloxylation of 1,3-Dienes and Related Reactions
Intramolecular Amination, Alkoxylation of Acyloxylation of Alkynes
Tandem Intramolecular Amination, Alkoxylation, or Acyloxylation-Allylation of Alkynes and Allenes
Tandem Intramolecular Amination, Alkoxylation, or Acyloxylation-Carbonylation of Alkynes
Intramolecular Amination or Alkoxylation of Alkenes
Tandem Intramolecular Amination or Alkoxylation-Carbonylation of Alkenes and Allenes
Reductive Cyclization with Diynes and Enynes
Cycloisomerization of Diynes and Enynes
Cycloaddition of Aziridines with Carbodiimides
Telomerization of 1,3-Dienes with Nucleophiles
WACKER Process
Preparation of Ketones from Alcohols or Derivatives via a (-Hydride Elimination
Preparation of ((-Unsaturated Carbonyl Derivatives via a (-Hydride Elimination
Preparation of (-Diketones Derivatives via an Oxidative Rearrangement of a Propargyl Acetate
Carbonylation
Isomerization of Alkynes
Addition of Thiols to Alkynes
Preparation of Allylic Acetates from Alkynes by Tandem Redox-Addition
Tandem Cyclization-Capture Process of Enynes
Aldol-Like Condensation of Enol Esters with Aldehydes
Addition of Fluoroalkyl Iodides to Alkenes or Alkynes via a Pd(I) Species
Intermolecular Tandem Carbonylation-Coupling-Cyclization Process of Aryl Halides with Terminal Alkynes.Intramolecular Coupling of Aryl Halides with Arenes
Tandem Intramolecular Alkoxylation-Vinylation of Alkenes
Carbonylative [2+2] Cycloaddition
Dicarboalkoxylation of Alkenes
Addition of Pronucleophile
Abbreviations
Introduction
Graphical Abstracts of Reaction Numbers (RXN)
12.

図書

図書
Robert Thornton Morrison, Robert Neilson Boyd
出版情報: Boston, Mass. : Allyn and Bacon, c1983  xxiv, 1370 p. ; 26 cm
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Structure and Properties / 1:
Methane / 2:
Energy of Activation
Transition State
Alkanes / 3:
Free-Radical Substitution
Stereochemistry I / 4:
Stereoisomers
Alkyl Halides / 5:
Nucleophilic Aliphatic Substitution
Alcohols and Ethers / 6:
Role of the Solvent / 7:
Secondary Bonding
Alkenes I / 8:
Structure and Preparation
Elimination
Alkenes II / 9:
Reactions of the Carbon-Carbon Double Bond
Electrophilic and Free-Radical Addition
Stereochemistry II / 10:
Stereoselective and Stereospecific Reactions
Conjugation and Resonance / 11:
Dienes
Alkynes / 12:
Alicyclic Compounds / 13:
Aromaticity / 14:
Benzene
Electrophilic Aromatic Substitution / 15:
Aromatic-Aliphatic Compounds / 16:
Arenes and Their Derivatives
Spectroscopy and Structure / 17:
Aldehydes and Ketones / 18:
Nucleophilic Addition
Carboxylic Acids / 19:
Functional Derivatives of Carboxylic Acids / 20:
Nucleophilic Acyl Substitution
Carbanions I / 21:
Amines I / 22:
Preparation and Physical Properties
Amines II / 23:
Reactions
Phenols / 24:
Carbanions II / 25:
Aryl Halides / 26:
Nucleophilic Aromatic Substitution
a,B-Unsaturated Carbonyl Compounds / 27:
Conjugate Addition
Molecular Orbitals / 28:
Orbital Symmetry
Symphoria / 29:
Neighboring Group Effects
Catalysis by Transition Metal Complexes
Heterocyclic Compounds / 30:
Macromolecules / 31:
Polymers and Polymerization
Stereochemistry III / 32:
Enantiotopic and Diastereotopic Ligands and Fats
Lipids / 33:
Fats and Steroids
Carbohydrates I / 34:
Monosaccharides
Carbohydrates II / 35:
Disaccharides and Polysaccharides
Proteins and Nucleic Acids / 36:
Molecular Biology
Structure and Properties / 1:
Methane / 2:
Energy of Activation
13.

図書

図書
A. P. Ryles, K. Smith, and R. S. Ward
出版情報: Chichester ; New York : Wiley, c1980  xiv, 306 p. ; 24 cm
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14.

図書

図書
edited by Shohei Inoue, Noboru Yamazaki
出版情報: Tokyo : Kodansha, 1981  xi, 280 p. ; 24 cm
シリーズ名: Kodansha scientific books
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15.

図書

図書
Penny A. Chaloner
出版情報: London ; Boston : Butterworths, 1986  1002 p. ; 24 cm
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16.

図書

図書
by H. L. Heys ; with a foreword by E. D. Hughes
出版情報: London : Harrap, 1960  236 p ; 23 cm
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17.

図書

図書
W.A. Waters
出版情報: London : Methuen , New York : Wiley, 1964  152 p. ; 23 cm
シリーズ名: Methuen's monographs on chemical subjects
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18.

図書

図書
edited by Saul Patai
出版情報: London : Wiley, 1977  2 v. (xv, 1343 p) ; 24 cm
シリーズ名: The Chemistry of functional groups ; supplement A; 6-1,2
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19.

図書

図書
Archibald J. Baker ... [et al.]
出版情報: London : Heyden, c1967  25, 60 p. ; 28 cm
シリーズ名: Spectroscopy in education series ; v. 4
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20.

図書

図書
by Bruno Jirgensons
出版情報: Amsterdam : Elsevier, 1958  xiv, 655 p. ; 24 cm
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21.

図書

図書
Miloš Hudlický
出版情報: Washington, DC : American Chemical Society, 1990  xx, 433 p. ; 24 cm
シリーズ名: ACS monograph ; no. 186
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Oxidation Agents
Dehydrogenations
Oxidations
Preparative Procedures
Oxidation Agents
Dehydrogenations
Oxidations
22.

図書

図書
by M.R. Rifi and Frank H. Covitz
出版情報: New York : M. Dekker, 1974  viii, 417 p. ; 24 cm
シリーズ名: Techniques and applications in organic synthesis
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23.

図書

図書
Alsoph H. Corwin, Maurice M. Bursey
出版情報: London : Addison-Wesley, 1966  xviii, 746 p. ; 22 cm
シリーズ名: Addison-Wesley world student series
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24.

図書

図書
edited by P. Zuman
出版情報: London : Plenum Publishing Co., 1970  ix, 530 p. ; 25 cm
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25.

図書

図書
[by] R. Foster
出版情報: London ; New York : Academic Press, 1969  xii, 470 p. ; 24 cm
シリーズ名: Organic chemistry : a series of monographs ; v. 15
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26.

図書

図書
by W. Mansfield Clark
出版情報: Baltimore : Williams & Wilkins, c1960  xi, 584 p. ; 24 cm
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27.

図書

図書
Lionel Salem
出版情報: Reading, Mass. : W.A. Benjamin, 1966  xvi, 576 p. ; 24 cm
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28.

図書

図書
Petr Zuman, With foreword by J. Heyrovsky
出版情報: New York : Plenum Press, 1967  xvi, 384 p. ; 24 cm
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29.

図書

図書
[by] C. David Gutsche [and] Daniel J. Pasto
出版情報: Englewood Cliffs, N.J. : Prentice-Hall, [1975]  viii, 1240 p. ; 25 cm
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30.

図書

図書
by Fritz Feigl ; translated by Ralph E. Oesper
出版情報: Amsterdam ; New York : Elsevier Pub. Co , Tokyo : Maruzen, 1961  675 p. ; 22 cm
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31.

図書

図書
George C. Levy, Robert L. Lichter
出版情報: New York : Wiley, c1979  ix, 221 p. ; 24 cm
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32.

図書

図書
William J. le Noble
出版情報: New York : M. Dekker, 1974  xvii, 976 p. ; 25 cm
シリーズ名: Studies in Organic Chemistry ; v. 3
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33.

図書

図書
[by] Donald J. Cram [and] George S. Hammond
出版情報: New York : McGraw-Hill, [c1964]  x, 846 p. ; 24 cm
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34.

図書

図書
editors: David Fox, Mortimer M. Labes and Arnold Weissberger
出版情報: New York : Interscience Publishers, 1963-1967  3 v. ; 24 cm
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35.

図書

図書
M. Pesez and J. Bartos
出版情報: New York : M. Dekker, c1974  xiv, 672 p. ; 24 cm
シリーズ名: Clinical and biochemical analysis ; v. 1
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36.

図書

図書
Christian Reichardt
出版情報: Weinheim, Federal Republic of Germany ; New York, NY, USA : VCH, c1988  xxii, 534 p. ; 25 cm
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目次情報: 続きを見る
Introduction
Solute-Solvent Interactions
Classification of Solvents
Solvent Effects on the Position of Homogeneous Chemical Equilibria
Solvent Effects on the Rate of Homogeneous Chemical Reactions
Solvent Effects on Absorption Spectra of Organic Compounds
Empirical Parameters of Solvent Polarity
Appendix
References
Introduction
Solute-Solvent Interactions
Classification of Solvents
37.

図書

図書
Edwin S. Gould
出版情報: New York : Holt, c1959  790 p ; 25 cm
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38.

図書

図書
Michael J. S. Dewar and Ralph C. Dougherty
出版情報: New York : Plenum Press, c1975  xiii, 576 p. ; 23 cm
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39.

図書

図書
[by] Michael J.S. Dewar
出版情報: New York : McGraw-Hill, c1969  xiv, 484 p. ; 23 cm
シリーズ名: McGraw-Hill series in advanced chemistry
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40.

図書

図書
Alan H. Haines
出版情報: London : Academic, 1988  xx, 467 p ; 24 cm
シリーズ名: Best synthetic methods
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41.

図書

図書
Beilstein, Friedrich Konrad, 1838-1906 ; Prager, Bernhard ; Jacobson, Paul, 1859-1923 ; Richter, Friedrich, 1896-1961 ; Deutsche Chemische Gesellschaft
出版情報: Berlin : J. Springer, 1918-1940  31 v. in 33 ; 25 cm
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42.

図書

図書
Saul Patai
出版情報: Chichester [England] ; New York : Wiley, 1989  vii, 455 p. ; 24 cm
シリーズ名: The Chemistry of functional groups
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43.

図書

図書
Beilstein, Friedrich Konrad, 1838-1906 ; Richter, Friedrich, 1896-1961 ; Deutsche Chemische Gesellschaft
出版情報: Berlin : J. Springer, 1928-1940  v. ; 25 cm
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44.

図書

図書
Kenneth B. Wiberg
出版情報: New York ; London : Wiley, c1964  viii, 591 p. ; 24 cm
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45.

図書

図書
by S.C. Nyburg
出版情報: New York : Academic Press, 1961  xii, 434 p. ; 24 cm
シリーズ名: Organic and biological chemistry : a series of monographs ; 4
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46.

図書

図書
by Frank J. Welcher, Erwin Boschmann
出版情報: Huntington, N.Y. : R. E. Krieger, 1979  xvi, 614 p. ; 24 cm
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47.

図書

図書
Philip S. Bailey, Jr., and Christina A. Bailey
出版情報: Boston : Allyn and Bacon, c1981  xvi, 429 p. ; 24 cm
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48.

図書

図書
Ralph J. Fessenden, Joan S. Fessenden
出版情報: Boston, Mass. : W. Grant Press, c1982  xvii, 1069 p. ; 26 cm
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49.

図書

図書
Marye Anne Fox, James K. Whitesell
出版情報: Boston : Jones and Bartlett, c1994  xxvi, 870 p. ; 29 cm
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目次情報: 続きを見る
Structure and Bonding in Alkanes / 1:
Alkenes, Aromatic Hydrocarbons, and Alkynes / 2:
Functional Groups Containing Heteroatoms / 3:
Chromatography and Spectroscopy / 4:
Stereochemistry / 5:
Understanding Organic Reactions / 6:
Mechanisms of Organic Reactions / 7:
Substitution by Nucleophiles at sp3-Hybridized Carbon / 8:
Elimination Reactions / 9:
Addition to Carbon-Carbon Multiple Bonds / 10:
Electrophilic Aromatic Substitution / 11:
Nucleophilic Addition and Substitution at Carbonyl Groups / 12:
Substitution Alpha to Carbonyl Groups / 13:
Skeletal-Rearrangement Reactions / 14:
Multistep Syntheses / 15:
Polymeric Materials / 16:
Naturally Occurring Oxygen-Containing Compounds / 17:
Naturally Occurring Nitrogen-Containing Compounds / 18:
Noncovalent Reactions and Molecular Recognition / 19:
Catalyzed Reactions / 20:
Cofactors for Biological Redox Reactions / 21:
Energy Storage in Organic Molecules / 22:
Molecular Basis for Drug Action / 23:
Structure and Bonding in Alkanes / 1:
Alkenes, Aromatic Hydrocarbons, and Alkynes / 2:
Functional Groups Containing Heteroatoms / 3:
50.

図書

図書
John McMurry
出版情報: Pacific Grove, Calif. : Brooks/Cole Pub. Co., c1994  xx, 536, 16 p. ; 25 cm
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目次情報: 続きを見る
Preface
A Note for Students
Structure and Bonding; Acids and Bases / 1:
Atomic Structure / 1.1:
Electron Configuration of Atoms / 1.2:
Development of Chemical Bonding Theory / 1.3:
The Nature of Chemical Bonds / 1.4:
Forming Covalent Bonds: Valence Bond Theory / 1.5:
Hybridization: sp[superscript 3] Orbitals and the Structure of Methane / 1.6:
Hybridization: sp[superscript 3] Orbitals and the Structure of Ethane / 1.7:
Hybridization: sp[subscript 2] Orbitals and the Structure of Ethylene / 1.8:
Hybridization: sp Orbitals and the Structure of Acetylene / 1.9:
Polar Covalent Bonds: Electronegativity / 1.10:
Acids and Bases: The Bronsted--Lowry Definition / 1.11:
Acids and Bases: The Lewis Definition / 1.12:
The Nature of Organic Compounds: Alkanes / 2:
Functional Groups / 2.1:
Alkanes and Alkyl Groups: Isomers / 2.2:
Naming Branched-Chain Alkanes / 2.3:
Properties of Alkanes / 2.4:
Conformations of Ethane / 2.5:
Drawing Chemical Structures / 2.6:
Cycloalkanes / 2.7:
Cis--Trans Isomerism in Cycloalkanes / 2.8:
Conformations of Some Cycloalkanes / 2.9:
Axial and Equatorial Bonds in Cyclohexane / 2.10:
Conformational Mobility of Cyclohexane / 2.11:
The Nature of Organic Reactions: Alkenes / 3:
Naming Alkenes / 3.1:
Electronic Structure of Alkenes / 3.2:
Cis--Trans Isomers of Alkenes / 3.3:
Sequence Rules: The E,Z Designation / 3.4:
Kinds of Organic Reactions / 3.5:
How Reactions Occur: Mechanisms / 3.6:
The Mechanism of an Organic Reaction: Addition of HCl to Ethylene / 3.7:
Describing a Reaction: Reaction Energy Diagrams and Transition States / 3.8:
Describing a Reaction: Intermediates / 3.9:
Reactions of Alkenes and Alkynes / 4:
Addition of HX to Alkenes: Hydrohalogenation / 4.1:
Orientation of Alkene Addition Reactions: Markovnikov's Rule / 4.2:
Carbocation Structure and Stability / 4.3:
Addition of H[subscript 2]O to Alkenes: Hydration / 4.4:
Addition of X[subscript 2] to Alkenes: Halogenation / 4.5:
Addition of H[subscript 2] to Alkenes: Hydrogenation / 4.6:
Oxidation of Alkenes: Hydroxylation and Cleavage / 4.7:
Biological Addition Reactions of Alkenes / 4.8:
Addition of Radicals to Alkenes: Polymers / 4.9:
Conjugated Dienes / 4.10:
Stability of Allylic Carbocations: Resonance / 4.11:
Drawing and Interpreting Resonance Forms / 4.12:
Alkynes and Their Reactions / 4.13:
Aromatic Compounds / 5:
Structure of Benzene: The Kekule Proposal / 5.1:
Structure of Benzene: The Resonance Proposal / 5.2:
Naming Aromatic Compounds / 5.3:
Electrophilic Aromatic Substitution Reactions: Bromination / 5.4:
Other Electrophilic Aromatic Substitution Reactions / 5.5:
The Friedel--Crafts Alkylation and Acylation Reactions / 5.6:
Substituent Effects in Electrophilic Aromatic Substitution / 5.7:
An Explanation of Substituent Effects / 5.8:
Oxidation and Reduction of Aromatic Compounds / 5.9:
Polycyclic Aromatic Hydrocarbons / 5.10:
Organic Synthesis / 5.11:
Stereochemistry / 6:
Stereochemistry and the Tetrahedral Carbon / 6.1:
The Reason for Handedness in Molecules: Chirality / 6.2:
Optical Activity / 6.3:
Specific Rotation / 6.4:
Pasteur's Discovery of Enantiomers / 6.5:
Sequence Rules for Specifying Configuration / 6.6:
Diastereomers / 6.7:
Meso Compounds / 6.8:
Molecules with More Than Two Stereocenters / 6.9:
Racemic Mixtures and the Resolution of Enantiomers / 6.10:
Physical Properties of Stereoisomers / 6.11:
A Brief Review of Isomerism / 6.12:
Chirality in Nature / 6.13:
Alkyl Halides / 7:
Naming Alkyl Halides / 7.1:
Preparing Alkyl Halides / 7.2:
Reactions of Alkyl Halides: Grignard Reagents / 7.3:
Nucleophilic Substitution Reactions / 7.4:
The S[subscript N]2 Reaction / 7.5:
The S[subscript N]1 Reaction / 7.6:
Eliminations: The E2 Reaction / 7.7:
Eliminations: The E1 Reaction / 7.8:
A Summary of Reactivity: S[subscript N]1, S[subscript N]2, E1, E2 / 7.9:
Substitution Reactions in Living Organisms / 7.10:
Alcohols, Phenols, and Ethers / 8:
Naming Alcohols, Phenols, and Ethers / 8.1:
Properties of Alcohols, Phenols, and Ethers: Hydrogen Bonding / 8.2:
Properties of Alcohols and Phenols: Acidity / 8.3:
Synthesis of Alcohols / 8.4:
Reactions of Alcohols / 8.5:
Synthesis and Reactions of Phenols / 8.6:
Synthesis and Reactions of Ethers / 8.7:
Cyclic Ethers: Epoxides / 8.8:
Thiols and Sulfides / 8.9:
Aldehydes and Ketones: Nucleophilic Addition Reactions / 9:
The Nature of Carbonyl Compounds / 9.1:
Naming Aldehydes and Ketones / 9.2:
Synthesis of Aldehydes and Ketones / 9.3:
Oxidation of Aldehydes / 9.4:
Nucleophilic Addition Reactions of Aldehydes and Ketones: Reduction / 9.5:
Nucleophilic Addition of Water: Hydration / 9.6:
Nucleophilic Addition of Alcohols: Acetal Formation / 9.7:
Nucleophilic Addition of Amines: Imine Formation / 9.8:
Nucleophilic Addition of Grignard Reagents: Alcohol Formation / 9.9:
Conjugate Nucleophilic Addition Reactions / 9.10:
Some Biological Nucleophilic Addition Reactions / 9.11:
Carboxylic Acids and Derivatives / 10:
Naming Carboxylic Acids and Derivatives / 10.1:
Occurrence and Properties of Carboxylic Acids / 10.2:
Synthesis of Carboxylic Acids / 10.3:
Nucleophilic Acyl Substitution Reactions / 10.4:
Reactions of Carboxylic Acids / 10.5:
Chemistry of Acid Halides / 10.6:
Chemistry of Acid Anhydrides / 10.7:
Chemistry of Esters / 10.8:
Chemistry of Amides / 10.9:
Chemistry of Nitriles / 10.10:
Polymers from Carbonyl Compounds: Nylons and Polyesters / 10.11:
Carbonyl Alpha-Substitution Reactions and Condensation Reactions / 11:
Keto--Enol Tautomerism / 11.1:
Reactivity of Enols: The Mechanism of Alpha-Substitution Reactions / 11.2:
Alpha Halogenation of Aldehydes and Ketones / 11.3:
Acidity of Alpha Hydrogen Atoms: Enolate Ion Formation / 11.4:
Reactivity of Enolate Ions / 11.5:
Alkylation of Enolate Ions / 11.6:
Carbonyl Condensation Reactions / 11.7:
Condensations of Aldehydes and Ketones: The Aldol Reaction / 11.8:
Dehydration of Aldol Products: Synthesis of Enones / 11.9:
Condensations of Esters: The Claisen Condensation Reaction / 11.10:
Biological Carbonyl Reactions / 11.11:
Amines / 12:
Naming Amines / 12.1:
Structure and Properties of Amines / 12.2:
Basicity of Amines / 12.3:
Synthesis of Amines / 12.4:
Reactions of Amines / 12.5:
Heterocyclic Amines / 12.6:
Alkaloids: Naturally Occurring Amines / 12.7:
Structure Determination / 13:
Infrared Spectroscopy and the Electromagnetic Spectrum / 13.1:
Infrared Spectroscopy of Organic Molecules / 13.2:
Ultraviolet Spectroscopy / 13.3:
Interpreting Ultraviolet Spectra: The Effect of Conjugation / 13.4:
Nuclear Magnetic Resonance Spectroscopy / 13.5:
The Nature of NMR Absorptions / 13.6:
Chemical Shifts / 13.7:
Chemical Shifts in [superscript 1]H NMR Spectra / 13.8:
Integration of [superscript 1]H NMR Spectra: Proton Counting / 13.9:
Spin--Spin Splitting in [superscript 1]H NMR Spectra / 13.10:
Uses of [superscript 1]H NMR Spectra / 13.11:
[superscript 13]C NMR Spectroscopy / 13.12:
Biomolecules: Carbohydrates / 14:
Classification of Carbohydrates / 14.1:
Configurations of Monosaccharides: Fischer Projections / 14.2:
D,L Sugars / 14.3:
Configurations of Aldoses / 14.4:
Cyclic Structures of Monosaccharides: Hemiacetal Formation / 14.5:
Monosaccharide Anomers: Mutarotation / 14.6:
Reactions of Monosaccharides / 14.7:
Polysaccharides / 14.9:
Other Important Carbohydrates / 14.10:
Cell-Surface Carbohydrates and Carbohydrate Vaccines / 14.11:
Biomolecules: Amino Acids, Peptides, and Proteins / 15:
Structures of Amino Acids / 15.1:
Isoelectric Points / 15.2:
Peptides and Proteins / 15.3:
Covalent Bonding in Peptides / 15.4:
Peptide Structure Determination: Amino Acid Analysis / 15.5:
Peptide Sequencing: The Edman Degradation / 15.6:
Peptide Synthesis / 15.7:
Classification of Proteins / 15.8:
Protein Structure / 15.9:
Enzymes / 15.10:
How Do Enzymes Work? Citrate Synthase / 15.11:
Biomolecules: Lipids and Nucleic Acids / 16:
Lipids / 16.1:
Fats and Oils / 16.2:
Soaps / 16.3:
Phospholipids / 16.4:
Steroids / 16.5:
Nucleic Acids and Nucleotides / 16.6:
Structure of DNA / 16.7:
Base Pairing in DNA: The Watson--Crick Model / 16.8:
Nucleic Acids and Heredity / 16.9:
Replication of DNA / 16.10:
Structure and Synthesis of RNA: Transcription / 16.11:
RNA and Protein Biosynthesis: Translation / 16.12:
Sequencing DNA / 16.13:
The Polymerase Chain Reaction / 16.14:
The Organic Chemistry of Metabolic Pathways / 17:
An Overview of Metabolism and Biochemical Energy / 17.1:
Catabolism of Fats: [beta]-Oxidation Pathway / 17.2:
Catabolism of Carbohydrates: Glycolysis / 17.3:
The Citric Acid Cycle / 17.4:
Catabolism of Proteins: Transamination / 17.5:
The Organic Chemistry of Metabolic Pathways: A Summary / 17.6:
Appendixes
Nomenclature of Polyfunctional Organic Compounds / A:
Glossary / B:
Answers to Selected In-Chapter Problems / C:
Index
Preface
A Note for Students
Structure and Bonding; Acids and Bases / 1:
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