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1.

図書

図書
Società chimica italiana, Divisione di chimica organica
出版情報: [Roma] : Società chimica italiana, 1999  518 p. ; 24 cm
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2.

図書

図書
Mark A. Rizzacasa and Michael Perkins
出版情報: Sheffield, [Eng.] ; Sheffield Academic , Malden, Ma. ; Blackwell Science , 2000  xii, 236 p. ; 24 cm
シリーズ名: Postgraduate chemistry series
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3.

図書

図書
Susan McMurry [著]
出版情報: Belmont, Calif. : Brooks/Cole , 東京 : 東京化学同人 (発売), 2005.3  868p ; 28cm
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4.

図書

図書
Michael B. Smith
出版情報: Boca Raton : CRC Press, Taylor & Francis, c2011  xvii, 1574 p. ; 26 cm
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5.

図書

図書
Ursula Bünzli-Trepp
出版情報: Lausanne : EPFL Press, c2007  ix, 636 p. ; 30 cm.
シリーズ名: Fundamental sciences ; Chemistry
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目次情報: 続きを見る
Directions for Use of the Book / 1:
Fundamentals / 2:
Nomenclature terms and definitions used in the Book / 2.1:
Conventions for enclosing marks and vowels in names / 2.2:
Enclosing marks / 2.2.1:
Vowels / 2.2.2:
Guide to Name Construction and Name Interpretation / 3:
General procedure and choice of the senior compound class (choice of the principal group) / 3.1:
Nomenclature types / 3.2:
Substitutive nomenclature / 3.2.1:
Conjunctive nomenclature / 3.2.2:
Multiplicative nomenclature: compounds with identical structural units / 3.2.3:
Additive nomenclature / 3.2.4:
Subtractive nomenclature / 3.2.5:
Functional-class nomenclature / 3.2.6:
Determination of the molecular-skeleton parent / 3.3:
Numbering of the molecular-skeleton parent and of other structure components / 3.4:
Alphabetical order of prefixes or parent-substituent names / 3.5:
Molecular-Skeleton Parents / 4:
Preliminary notes / 4.1:
Hydrocarbon chains / 4.2:
Heterochains / 4.3:
Heterochains with irregularly placed heteroatoms: replacement nomenclature ('a' nomenclature) / 4.3.1:
Heterochains with regularly placed heteroatoms: homogeneous and heterogeneous heterochains / 4.3.3:
Carbomonocycles / 4.4:
Heteromonocycles / 4.5:
Heteromonocycles with compulsory trivial names / 4.5.1:
Heteromonocycles with ten or fewer ring members: extended Hantzsch-Widman nomenclature / 4.5.3:
Heteromonocycles with more than ten ring members: replacement nomenclature ('a' nomenclature) / 4.5.4:
Silicon-containing heteromonocycles / 4.5.5:
Fused polycycles (carbo- and heterocycles) / 4.6:
Fused polycycles with compulsory semitrivial or trivial names / 4.6.1:
Fused polycycles consisting of a parent component and attached components: fusion names / 4.6.3:
Fused polycycles with replacement names ('a' names) / 4.6.4:
Von Baeyer bridged polycycles (carbo- and heterocycles) / 4.7:
Bridged fused polycycles (carbo- and heterocycles) / 4.8:
Spiropolycycles (carbo- and heterocycles) / 4.9:
Spiropolycycles with carbomonocycle or heteromonocycle components / 4.9.1:
Spiropolycycles with at least one fused-polycycle component or one von Baeyer bridged-polycycle component / 4.9.3:
Ring assemblies of identical ring components (carbo- and heterocycles) / 4.10:
Substituent Prefixes / 5:
Prefixes of mononuclear substituents / 5.1:
Prefixes of hydrocarbon-chain substituents / 5.3:
Prefixes of heterochain substituents / 5.4:
Prefixes of carbocycle substituents / 5.5:
Prefixes of heterocycle substituents / 5.6:
Prefixes of ring-assembly substituents / 5.7:
Prefixes of composite substituents: choice of the parent substituent / 5.8:
Prefixes of carbonyl-containing substituents and analogs / 5.9:
Compound Classes / 6:
Radicals / 6.1:
Radical center at a molecular-skeletal parent / 6.2.1:
Radical center at a characteristic group / 6.2.3:
Polyradicals / 6.2.4:
Cations / 6.3:
Cation center by the formal addition of electrophiles E[superscript +] / 6.3.1:
Cation center by the formal removal of hydride ions H[superscript -] / 6.3.3:
Cation center resulting from skeletal bonding of a heteroatom / 6.3.4:
Cation center in spiropolycycles / 6.3.5:
Cation substituents (prefixes) / 6.3.6:
Polycations / 6.3.7:
Anions / 6.4:
Anion center by the formal removal of protons H[superscript +] / 6.4.1:
Anion center by the formal addition of hydride ions H[superscript -] / 6.4.3:
Anion substituents (prefixes) / 6.4.4:
Polyanions / 6.4.5:
Zwitterions / 6.5:
Radical ions / 6.6:
Carboxylic, carbothioic, carboselenoic, carbotelluroic, carbohydrazonic, carboximidic, and corresponding carboperoxoic acids and salts / 6.7:
Carboxylic acids / 6.7.1:
Carbothioic, carboselenoic, carbotelluroic, carbohydrazonic, and carboximidic acids / 6.7.3:
Carboperoxoic acids (peroxy acids) and their chalcogeno, hydrazono, and imido replacement analogs / 6.7.4:
Salts of carboxylic acids and of their chalcogeno, hydrazono, imido, and peroxy replacement analogs / 6.7.5:
Sulfonic, sulfinic, and sulfenic acids, selenonic, seleninic, and selenenic acids, telluronic, tellurinic, and tellurenic acids, their chalcogeno, hydrazono, imido, and peroxy replacement analogs, and corresponding salts / 6.8:
C-Oxoacids: carbonic and formic acid and their replacement analogs and corresponding salts / 6.9:
S-, Se-, Te-, and N-Oxoacids / 6.10:
P- and As-Oxoacids / 6.11:
Sb-, Bi-, Si-, and B-Oxoacids / 6.12:
Anhydrides / 6.13:
Esters and lactones / 6.14:
Acid halides / 6.15:
Amides, lactams, cyclic imides, and amidines / 6.16:
Hydrazides / 6.17:
Nitriles / 6.18:
Aldehydes and their oxime and hydrazone derivatives / 6.19:
Ketones and their oxime and hydrazone derivatives / 6.20:
Alcohols and phenols / 6.21:
Hydroperoxides / 6.22:
Amines / 6.23:
Imines / 6.24:
Nitrogen compounds / 6.25:
Phosphorus and arsenic compounds / 6.26:
Antimony and bismuth compounds / 6.27:
Boron compounds / 6.28:
Silicon, germanium, tin, and lead compounds / 6.29:
Oxygen compounds / 6.30:
Sulfur, selenium, and tellurium compounds / 6.31:
Carbon compounds / 6.32:
Halogen compounds / 6.33:
Organometallic and coordination compounds / 6.34:
Appendixes
Specialist nomenclatures / A.1:
Alkaloids / A.1.1:
Amino acids and peptides / A.1.3:
Carbohydrates / A.1.4:
Cyclitols / A.1.5:
Nucleosides, nucleotides, and nucleic acids / A.1.6:
Steroids / A.1.7:
Terpenes, carotenoids, and retinoids / A.1.8:
Vitamins / A.1.9:
Porphyrins and bile pigments / A.1.10:
Polymers / A.1.11:
References for specific compound classes, Internet addresses, and nomenclature software / A.1.12:
Multiplying affixes / A.2:
Modifying syllables / A.3:
Heteroatom syllables and element names / A.4:
Indicated H atom 'H' (indicated hydrogen) / A.5:
Configuration descriptors in names / A.6:
Definitions / A.6.1:
The CIP system for the specification of the configuration of a stereogenic center, axis or plane, or double bond / A.6.2:
Stereodescriptors for the denotation of the absolute and relative configuration in names / A.6.3:
Configuration of organometallic and coordination compounds / A.6.4:
Lambda ([lambda]) convention / A.7:
Isotopically modified compounds / A.8:
Isotopically modified compounds: IUPAC Recommendations / A.8.1:
Isotopically modified compounds: CA Guidelines / A.8.3:
Index
Directions for Use of the Book / 1:
Fundamentals / 2:
Nomenclature terms and definitions used in the Book / 2.1:
6.

図書

図書
Maitland Jones, Jr. and Henry L. Gingrich
出版情報: New York : Norton , 東京 : 東京化学同人(発売), 2006, c2005  x, 803 p. ; 28 cm
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7.

図書

図書
edited by Thomas J.J. Müller and Uwe H.F. Bunz
出版情報: Weinheim : Wiley-VCH, c2007  xx, 591 p. ; 25 cm.
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目次情報: 続きを見る
Preface
List of Contributors
3-D Carbon-rich ?-Systems - Nanotubes and Segments / Part I:
Functionalization of Carbon Nanotubes / Andreas Hirsch ; Otto Vostrowsky1:
Introduction to Carbon Nanotubes - A New Carbon Allotrope / 1.1:
Covalent Functionalization / 1.2:
Noncovalent Exohedral Functionalization-Functionalization with Biomolecules / 1.4:
Endohedral Functionalization / 1.5:
Conclusions / 1.6:
Experimental / 1.7:
Cyclophenacene Cut Out of Fullerene / Yutaka Matsuo ; Eiichi Nakamura2:
Introduction / 2.1:
Synthesis of [10]Cyclophenacene ?-Conjugated Systems from [60]Fullerene / 2.2:
Conclusion / 2.3:
Strategic Advances in Chromophore and Materials Synthesis / 2.4:
Cruciform ?-Conjugated Oligomers / Frank Galbrecht ; Torsten W. Bünnagel ; Askin Bilge ; Ullrich Scherf ; Tony Farrell3:
Oligomers with a Tetrahedral Core Unit / 3.1:
Oligomers with a Tetrasubstituted Benzene Core / 3.3:
Oligomers with a Tetrasubstituted Biaryl Core / 3.4:
Design of ?-Conjugated Systems Using Organophosphorus Building Blocks / Philip W. Dyer ; Rgis Rau3.5:
Phosphole-containing ?-Conjugated Systems / 4.1:
Phosphine-containing ?-Conjugated Systems / 4.3:
Phosphaalkene- and Diphosphene-containing ?jugated Systems / 4.4:
Selected Experimental Procedures / 4.5:
Diversity-oriented Synthesis of Chromophores by Combinatorial Strategies and Multi-component Reactions / Thomas J. J. Müller5:
Combinatorial Syntheses of Chromophores / 5.1:
Novel Multi-component Syntheses of Chromophores / 5.3:
Conclusion and Outlook / 5.4:
Experimental Procedures / 5.5:
High-yield Synthesis of Shape-persistent Phenylene-Ethynylene Macrocycles / Sigurd Höger6:
Synthesis / 6.1:
Functional Materials via Multiple Noncovalent Interactions / Joseph R. Carlisle ; Marcus Weck6.3:
Biologically Inspired Materials via Multi-step Self-assembly / 7.1:
Small Molecule-based Multi-step Self-assembly / 7.3:
Polymer-based Self-assembly / 7.4:
Molecular Muscles, Switches and Electronics / 7.5:
Molecular Motors and Muscles / Sourav Saha ; J. Fraser Stoddart8:
Mechanically Interlocked Molecules as Artificial Molecular Machines / 8.1:
Chemically Induced Switching of the Bistable Rotaxanes / 8.3:
Electrochemically Controllable Bistable Rotaxanes / 8.4:
Photochemically Powered Molecular Switches / 8.5:
Diarylethene as a Photoswitching Unit of Intramolecular Magnetic Interaction / Kenji Matsuda ; Masahiro Irie8.6:
Photochromic Spin Coupler / 9.1:
Synthesis of Diarylethene Biradicals / 9.3:
Photoswitching Using Bis(3-thienyl)ethene / 9.4:
Reversed Photoswitching Using Bis(2-thienyl)ethene.9 / 9.5:
Preface
List of Contributors
3-D Carbon-rich ?-Systems - Nanotubes and Segments / Part I:
8.

図書

東工大
目次DB

図書
東工大
目次DB
T.W. Graham Solomons, Craig B. Fryhle, Robert G. Johnson [著] ; 池田正澄 [ほか] 監訳
出版情報: 東京 : 廣川書店, 2008.4  vii, 279p ; 26cm
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目次情報: 続きを見る
1. 有機化学の基礎 : 化学結合と分子構造 1
2. 代表的な炭素化合物 13
3. 有機化学反応序論 : 酸と塩基 19
4. アルカンとシクロアルカンの命名法と立体配座 27
5. 立体化学 : キラルな分子 39
6. イオン反応 : ハロゲン化アルキルの求核置換反応と脱離反応 51
7. アルケンとアルキンⅠ : 性質と合成.ハロゲン化アルキルの脱離反応 63
8. アルケンとアルキンⅡ : 付加反応 79
9. ラジカル反応 91
10. アルコール,エーテル,およびチオール 97
11. カルボニル化合物からアルコールの合成 : 酸化還元反応と有機金属化合物 109
12. 共役不飽和系 129
13. 芳香族化合物 141
14. 芳香族化合物の反応 147
15. アルデヒドとケトンⅠ : カルボニル基への求核付加 165
16. アルデヒドとケトンⅡ : エノールとエノラート 181
17. カルボン酸とその誘導体 : アシル炭素上の求核付加-脱離反応 197
18. β-ジカルボニル化合物の合成と反応 : エノラートの化学 213
19. アミン 231
20. フェノールとハロゲン化アリール : 芳香族求核置換反応 255
21. 炭水化物 265
22. 脂質 269
23. アミノ酸とタンパク質 273
24. 核酸とタンパク質合成 277
1. 有機化学の基礎 : 化学結合と分子構造 1
2. 代表的な炭素化合物 13
3. 有機化学反応序論 : 酸と塩基 19
9.

図書

図書
by E.E.Turner and Margaret M.Harris
出版情報: London : Longmans, Green, 1952  xi, 904p. ; 26cm
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10.

図書

図書
Maitland Jones, Jr. and Henry L. Gingrich
出版情報: New York : Norton , 東京 : 東京化学同人(発売), 2001, c2000  x, 787 p. ; 28 cm
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