2019-07-15

参考文献

一般（英語）

  1. [GNOC1993] International Union of Pure and Applied Chemistry. Organic Chemistry Division. Commission on Nomenclature of Organic Chemistry. A Guide to IUPAC Nomenclature of Organic Compounds, Recommendations 1993. Blackwell Scientific Publications, Oxford, UK (1993); Corrections to A Guide to IUPAC Nomenclature of Organic Compounds (IUPAC Recommendations 1993). Pure Appl. Chem. 71, 1327-1330 (1999).
    cf. url: https://www.acdlabs.com/iupac/nomenclature/ (Guide本編)
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/bibliog/errata.html (Corrections)
  2. [NOC1979] International Union of Pure and Applied Chemistry. Organic Chemistry Division. Commission on Nomenclature of Organic Chemistry. Nomenlature of Organic Chemistry, Sections A, B, C, D, E, F, and H, 1979 edition. Pergamon Press, Oxford, UK (1979).
    cf. url: https://www.acdlabs.com/iupac/nomenclature/
  3. [NIC1990] International Union of Pure and Applied Chemistry. Inorganic Chemistry Division. Commission on Nomenclature of Inorganic Chemistry. Nomenclature of Inorganic Chemistry, Recommendations 1990. Blackwell Scientific Publications, Oxford, UK (1990).
  4. [NIC1970] International Union of Pure and Applied Chemistry. Inorganic Chemistry Division. Commission on Nomenclature of Inorganic Chemistry. Nomenclature of Inorganic Chemistry, Second edition, Definitive Rules 1970. Pure Appl. Chem. 28, 1-110 (1971).
    cf. url: http://www.iupac.org/publications/pac/28/1/0001/
  5. Chemical Abstracts Service. Chemical Abstracts, Index Guide, Appendix IV. 1972; 1986; 1992; 1997.
  6. Chemical Abstracts Service. Index of Ring Systems, 1972; 1986; 1994.
  7. Chemical Abstracts Service. Index of Parent Compounds: Stereoparent Index, 1983.
  8. Chemical Abstracts Service. Introduction with Key and Discussion of the Naming of Chemical Compounds for Indexing, Chemical Abstracts 39, 5867-5975 (1945).
  9. [GCN] International Union of Pure and Applied Chemistry. Organic Chemistry Division. Commission on Nomenclature of Organic Chemistry and Commission on Physical Organic Chemistry. Glossary of Class Names of Organic Compounds and Reactive Intermediates Based on Structure (IUPAC Recommendations 1995). Pure Appl. Chem. 67, 1307-1375 (1995).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/class/
  10. [NOCT] International Union of Pure and Applied Chemistry. Organic Chemistry Division. Commission on Physical Organic Chemistry. Nomenclature for Organic Chemical Transformations (IUPAC Recommendations 1988). Pure Appl. Chem. 61, 725-768 (1989).
  11. [GTPOC] International Union of Pure and Applied Chemistry. Organic Chemistry Division. Commission on Physical Organic Chemistry. Glossary of Terms Used in Physical Organic Chemistry (IUPAC Recommendations 1994). Pure Appl. Chem. 66, 1007-1184 (1994).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/gtpoc/

一般（日本語）

  1. 日本化学会化合物命名小委員会，化合物命名法. 補訂５版 (1995)；補訂６版 (1998)；補訂７版 (2000).
  2. 平山健三，平山和雄訳著，有機化学・生化学命名法上. 改訂第２版. 南江堂，東京 (1988).
  3. 平山健三，平山和雄訳著，有機化学・生化学命名法下. 改訂第２版. 南江堂，東京 (1989).
  4. 山崎一雄訳，無機化学命名法 -IUPAC 1990年勧告-. 東京化学同人，東京 (1993).
  5. 中原勝儼訳，ACS無機・有機金属命名法. 丸善，東京 (1993).
  6. 文部省，日本化学会，学術用語集化学編（増訂２版），南江堂，東京 (1986)。
  7. 日本化学会編，標準化学用語辞典 縮刷版，丸善，東京 (1993).
  8. 久保亮五，長倉三郎，井口洋夫，江沢洋編集，理化学辞典 第４版，岩波書店，東京 (1987).
  9. J.Stenesh著，増田芳雄，中村運，加藤憲一，福村隆，神阪盛一郎訳，生理・生化学用語辞典，化学同人，京都 (1985).
  10. 文部省，日本薬学会，学術用語集薬学編，丸善，東京 (2000).

有機化学各論

  1. [HW] International Union of Pure and Applied Chemistry. Organic Chemistry Division. Commission on Nomenclature of Organic Chemistry. Revision of the Extented Hantzsch-Widman System of Nomenclature for Heteromonocycles (IUPAC Recommendations 1982). Pure Appl. Chem. 55, 409-416 (1983).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/hetero/HW.html
  2. [Lm] International Union of Pure and Applied Chemistry. Organic Chemistry Division. Commission on Nomenclature of Organic Chemistry. Treatment of Variable Valence in Organic Nomenclature (Lambda-Convention) (IUPAC Recommendations 1983). Pure Appl. Chem. 56, 769-778 (1984).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/hetero/Lm.html
  3. [RNRI] International Union of Pure and Applied Chemistry. Organic Chemistry Division. Commission on Nomenclature of Organic Chemistry. Revised Nomenclature for Radicals, Ions, Radical Ions, and Related Species (IUPAC Recommendations 1993). Pure Appl. Chem. 65, 1357-1455 (1993).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/ions/
  4. [FR] International Union of Pure and Applied Chemistry. Organic Chemistry Division. Commission on Nomenclature of Organic Chemistry. Nomenclature of Fused and Bridged Fused Ring Systems (IUPAC Recommendations 1998). Pure Appl. Chem. 70, 143-216 (1998).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/fusedring/
  5. [VB] International Union of Pure and Applied Chemistry. Organic Chemistry Division. Commission on Nomenclature of Organic Chemistry. Extension and Revision of the von Baeyer System for Naming Polycyclic Compounds (Including Bicyclic Compounds) (IUPAC Recommendations 1999). Pure Appl. Chem. 71, 513-529 (1999).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/vonBaeyer/
  6. [SP] International Union of Pure and Applied Chemistry. Organic Chemistry Division. Commission on Nomenclature of Organic Chemistry. Extension and Revision of the Nomenclature of Spiro Compounds (IUPAC Recommendations 1999). Pure Appl. Chem. 71, 531-558 (1999).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/spiro/
  7. F. Voegtle and P. Neumann, Zur Nomenklatur der Phane - II. Tetrahedron 26, 5847-5863 (1970).
  8. [PhI] International Union of Pure and Applied Chemistry. Organic Chemistry Division. Commission on Nomenclature of Organic Chemistry. Phane Nomenclature. Part I: Phane Parent Names (IUPAC Recommendations 1998). Pure Appl. Chem. 70, 1513-1545 (1998).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/phane/
  9. [PhII] International Union of Pure and Applied Chemistry. Organic Chemistry Division. Commission on Nomenclature of Organic Chemistry. Phane Nomenclature. Part II. Modification of the Degree of Hydrogenation and Substitution Derivatives of Phane Parent Hydrides (IUPAC Recommendations 2002). Pure Appl. Chem. 74, 809-834 (2002).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/phane2/
  10. [HY] International Union of Pure and Applied Chemistry. Organic Chemistry Division. Commission on Physical Organic Chemistry. Names for Hydrogen Atoms, Ions, and Groups, and for Reactions Involving Them. (IUPAC Recommendations 1988). Pure Appl. Chem. 60, 1115-1116 (1988).
  11. [Nt] International Union of Pure and Applied Chemistry. Organic Chemistry Division. Commission on Nomenclature of Organic Chemistry. Extention of Rules A-1.1 and A-2.5 Concerning Numerical Terms Used in Organic Chemical Nomenclature (IUPAC Recommendations 1986). Pure Appl. Chem. 58, 1693-1696 (1986).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/misc/numb.html
  12. [De] International Union of Pure and Applied Chemistry. Organic Chemistry Division. Commission on Nomenclature of Organic Chemistry. Nomenclature for Cyclic Organic Compounds with Contiguous Double Bonds (The δ-Convention) (IUPAC Recommendations 1988). Pure Appl. Chem. 60, 1395-1401 (1988).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/hetero/De.html
  13. [NOC-H] International Union of Pure and Applied Chemistry. Organic Chemistry Division. Commission on Nomenclature of Organic Chemistry. Nomenclature of Organic Chemistry. Section H: Isotopically Modified Compounds (First Edition) (IUPAC Approved Recommendations 1978). Pure Appl. Chem. 51, 353-380 (1978).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/sectionH/
  14. International Union of Pure and Applied Chemistry. Nomenclature and Terminology of Fullerenes: A Preliminary Survey. Pure Appl. Chem. 69, 1411-1434 (1997).
  15. [Fu] International Union of Pure and Applied Chemistry. Organic Chemistry Division. Commission on Nomenclature of Organic Chemistry. Nomenclature for the C60-Ih and C70-D5h(6) Fullerenes (IUPAC Recommendations 2002). Pure Appl. Chem. 74, 629-695 (2002).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/fullerene/
  16. [NOC-E] International Union of Pure and Applied Chemistry. Organic Chemistry Division. Commission on Nomenclature of Organic Chemistry. Nomenclature of Organic Chemistry, Section E: Stereochemistry (IUPAC Recommendations 1974). Pure Appl. Chem. 45, 11-30 (1976).
  17. [BTSC] International Union of Pure and Applied Chemistry. Organic Chemistry Division. Commission on Nomenclature of Organic Chemistry and Commission on Physical Organic Chemistry. Basic Terminology of Stereochemistry (IUPAC Recommendations 1996). Pure Appl. Chem. 68, 2193-2222 (1996).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/stereo/
  18. R. S. Cahn, C. K. Ingold, and V. Prelog, Specification of Molecular Chirality. Angew. Chem. Int. Ed. Engl. 5, 385-415 (1966) [errata: 5, 511(1966)].
  19. V. Prelog and G. Helmchen, Basic Principles of the CIP-System and Proposals for a Revision. Angew. Chem. Int. Ed. Engl. 21, 567-583 (1982).

無機化学各論

  1. International Union of Pure and Applied Chemistry. Inorganic Chemistry Division. Commission on Nomenclature of Inorganic Chemistry. Nomenclature of Inorganic Chemistry: II.1 - Isotopically Modified Compounds (IUPAC Recommendations 1981). Pure Appl. Chem. 53, 1887-1900 (1981).
  2. International Union of Pure and Applied Chemistry. Inorganic Chemistry Division. Commission on Nomenclature of Inorganic Chemistry. Nomenclature of Organometallic Compounds of the Transition Elements (IUPAC Recommendations 1999). Pure Appl. Chem. 71, 1557-1585 (1999).
  3. M. F. Brown, B. R. Cook, and T. E. Sloan, Stereochemical Notation in Coordination Chemistry. Mononuclear Complexes. Inorg. Chem. 14, 1273-1278 (1975).
  4. M. F. Brown, B. R. Cook, and T. E. Sloan, Stereochemical Notation in Coordination Chemistry: Mononuclear Complexes of Coordination Numbers Seven, Eight, and Nine. Inorg. Chem. 17, 1563-1568 (1978).
  5. [MU] International Union of Pure and Applied Chemistry. Inorganic Chemistry Division. Commission on Nomenclature of Inorganic Chemistry. Names of Muonium and Hydrogen Atoms and Their Ions. Pure Appl. Chem. 73, 377-380 (2001).

生化学

  1. [RF] IUPAC Commission on Nomenclature of Organic Chemistry. Revised Section F: Natural Products and Related Compounds (IUPAC Recommendations 1999). Pure Appl. Chem. 71, 587-643 (1999); Errata: Pure Appl. Chem. 76, 1283-1292 (2004).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/sectionF/ [本編1999]
    cf. url: http://pac.iupac.org/publications/pac/76/6/1283/ [Errata 2004]
  2. [Flv] IUPAC. Nomenclature of Flavonoids (IUPAC Recommendations 2017). Pure Appl. Chem. 90, 1429-1486 (2018).
  3. [3AA] IUPAC-IUB JCBN. Nomenclature and Symbolism for Amino Acids and Peptides (Recommendations 1983). Pure Appl. Chem. 56, 595-624 (1984).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/AminoAcid/
  4. [SymAA] IUPAC-IUB JCBN. Symbols for Amino-Acid Derivatives and Peptides (Rules Approved 1974). Pure Appl. Chem. 40, 315-331 (1975).
  5. [2AA] IUPAC-IUB CBN. Nomenclature of α-Amino Acids (Recommendations 1974). Biochemistry, 14, 449-462 (1975).
  6. IUPAC-IUB. A One-Letter Notation for Amino Acid Sequences (Definitive Rules 1971). Pure Appl. Chem. 31, 639-645 (1972).
  7. [Sec] IUPAC-IUBMB Newsletter 1999, Selenocysteine
    cf. url: https://www.qmul.ac.uk/sbcs/iubmb/newsletter/1999/item3.html
  8. [3S] IUPAC-IUB JCBN. Nomenclature of Steroids (Recommendations 1989). Pure Appl. Chem. 61, 1783-1822 (1989).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/steroid/
  9. [2S] IUPAC and IUB. Definitive Rules for Nomenclature of Steroids. Pure Appl. Chem. 31, 285-322 (1972).
  10. [VD] IUPAC-IUB JCBN. Nomenclature of Vitamin D. Pure Appl. Chem. 54, 1511-1516 (1982).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/misc/D.html
  11. [2-Carb] IUPAC-IUBMB JCBN. Nomenclature of Carbohydrates (Recommendations 1996). Pure Appl. Chem. 68, 1919-2008 (1996).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/2carb/
  12. [Carb] IUPAC-IUB CBN. Tentative Rules for Carbohydrate Nomenclature, Part I. Biochemistry, 10, 3983-4004 (1969).
  13. IUPAC-IUBMB JCBN. Nomenclature of Unsaturated Monosaccharides. Pure Appl. Chem., 54, 207-210 (1982).
  14. IUPAC-IUBMB JCBN. Nomenclature of Branched-Chain Monosaccharides. Pure Appl. Chem., 54, 211-215 (1982).
  15. [Cyc] IUPAC and IUB. Nomenclature of Cyclitols. Pure Appl. Chem., 37, 284-297 (1974).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/cyclitol/
  16. [TP] IUPAC-IUB JCBN. Nomenclature of Tetrapyrroles (Recommendations 1986). Pure Appl. Chem. 59, 779-832 (1987).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/tetrapyrrole/
  17. [Corr] IUPAC-IUB CBN. Nomenclature of Corrinoids (Rules Approved 1975). Pure Appl. Chem. 48, 495-502 (1976).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/misc/B12.html
  18. [Lip] IUPAC-IUB JCBN. The Nomenclature of Lipids (Recommendations 1976). Eur. J. Biochem. 79, 11-21 (1977).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/lipid/
  19. [GL] IUPAC-IUBMB JCBN. Nomenclature of Glycolipids (IUPAC Recommendations 1997). Pure Appl. Chem., 69, 2475-2487 (1997).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/misc/glylp.html
  20. [Carot] IUPAC and IUB. Nomenclature of Carotenoids. Pure Appl. Chem. 41, 407-431 (1975).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/carot/
  21. [Ret] IUPAC-IUB JCBN. Nomenclature of Retinoids. Pure Appl. Chem. 55, 721-726 (1983).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/misc/ret.html
  22. [Pr] IUPAC-IUBMB JCNB. Nomenclature of Prenols (Recommendations 1986). Pure Appl. Chem. 59, 683-689 (1987).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/misc/prenol.html
  23. [FA] IUPAC-IUB JCBN. Nomenclature and Symbols for Folic Acid and Related Compounds (Recommendations 1986). Pure Appl. Chem. 59, 883-836 (1987).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/misc/folic.html
  24. [VB6] IUPAC-IUB CBN. Definitive Nomenclature for Vitamins B-6 and Related Compounds (Definitive Rules 1972). Pure Appl. Chem. 33, 445-452 (1972).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/misc/B6.html
  25. [Toc] IUPAC-IUB JCBN. Nomenclature of Tocopherol and Related Compounds (Recommendations 1981). Pure Appl. Chem. 54, 1507-1510 (1982).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/misc/toc.html
  26. [Qu] IUPAC and IUB. Nomenclature of Quinones with Isoprenoid Side-Chains (Rules 1973). Pure Appl. Chem. 38, 439-447 (1974).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/misc/quinone.html
  27. [Nuc] IUPAC and IUB. Abbreviation and Symbols for Nucleic acids, Polynucleotide and Their Constituents (Rules Approved 1974). Pure Appl. Chem. 40, 278-290 (1974).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/misc/naabb.html
  28. [M] IUPAC and IUB. Trivial Names of Miscellaneous Compounds of Importance in Biochemistry (Tentative Rules). J. Biol. Chem. Chem. 241, 2987-2988 (1966).
  29. [P] IUPAC and IUB. Nomenclature of Phosphorus-Containing Compounds of Biochemical Importance (Recommendations 1976). Eur. J. Biochem. 79, 1-9 (1977).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/misc/phospho.html
  30. [LG] IUPAC-IUBMB JCNB. Nomenclature of Lignans and Neolignans (Recommendations 2000). Pure Appl. Chem. 72, 1493-1523 (2000).
    cf. url: https://www.qmul.ac.uk/sbcs/iupac/lignan/

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