2019-07-15

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  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).
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  5. Chemical Abstracts Service. Chemical Abstracts, Index Guide, Appendix IV. 1972; 1986; 1992; 1997.
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  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).
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  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).
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  1. “ú–{‰»Šw‰ï‰»‡•¨–½–¼¬ˆÏˆõ‰ïC‰»‡•¨–½–¼–@. •â’ù‚T”Å (1995)G•â’ù‚U”Å (1998)G•â’ù‚V”Å (2000).
  2. •½ŽRŒ’ŽOC•½ŽR˜a—Y–ó’˜C—L‹@‰»ŠwE¶‰»Šw–½–¼–@ã. ‰ü’ù‘æ‚Q”Å. “ì]“°C“Œ‹ž (1988).
  3. •½ŽRŒ’ŽOC•½ŽR˜a—Y–ó’˜C—L‹@‰»ŠwE¶‰»Šw–½–¼–@‰º. ‰ü’ù‘æ‚Q”Å. “ì]“°C“Œ‹ž (1989).
  4. ŽRèˆê—Y–óC–³‹@‰»Šw–½–¼–@ -IUPAC 1990”NŠ©-. “Œ‹ž‰»Šw“¯lC“Œ‹ž (1993).
  5. ’†Œ´Ÿ™V–óCACS–³‹@E—L‹@‹à‘®–½–¼–@. ŠÛ‘PC“Œ‹ž (1993).
  6. •¶•”ÈC“ú–{‰»Šw‰ïCŠwp—pŒêW‰»Šw•Òi‘’ù‚Q”ÅjC“ì]“°C“Œ‹ž (1986)B
  7. “ú–{‰»Šw‰ï•ÒC•W€‰»Šw—pŒêŽ«“T kü”ÅCŠÛ‘PC“Œ‹ž (1993).
  8. ‹v•Û—ºŒÜC’·‘qŽO˜YCˆäŒû—m•vC]‘ò—m•ÒWC—‰»ŠwŽ«“T ‘æ‚S”ÅCŠâ”g‘“XC“Œ‹ž (1987).
  9. J.Stenesh’˜C‘“c–F—YC’†‘º‰^C‰Á“¡Œ›ˆêC•Ÿ‘º—²C_ã·ˆê˜Y–óC¶—E¶‰»Šw—pŒêŽ«“TC‰»Šw“¯lC‹ž“s (1985).
  10. •¶•”ÈC“ú–{–òŠw‰ïCŠwp—pŒêW–òŠw•ÒCŠÛ‘PC“Œ‹ž (2000).

—L‹@‰»ŠwŠe˜_

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  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).
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  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).
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–³‹@‰»ŠwŠe˜_

  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).
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  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).

¶‰»Šw

  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).
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