IUPAC命名法
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IUPAC命名法
IUPAC已发布的命名法有:
有机化学命名法,E部:立体化学
有机化学命名法,F部:天然产物和有关化合物
有机化学命名法,H部:同位素标记化合物
修订的杂环命名法Hantzsch-Widman系统的延伸
对于有机化学的可变价的命名法(Lambda约定)
规则A-1.1和A-2.5的扩充,关于有机化学中的数字
具有累积双键的环状有机物命名法(Delta约定)
修订的基、离子、基离子及相关物种的命名法
有机化学类名和基与结构的反映中间产物的术语表
立体化学基本术语
稠环及桥稠环系统的命名法
芬命名法,第一部分:芬的母体名称
扩展及修订的命名多环化合物的von Baeyer系统(包括双环化合物)
扩展及修订的螺化合物的的命名法
修订的F部:天然产物和有关化合物
C60-Ih及C70-D5h(6)球碳的命名法
芬命名法,第二部分:加氢度的修正和芬母体取代产物
球碳的编号
参阅
国际化合物标识
IUPAC数值前缀
参考
^Nomenclature of organic chemistry, section E: stereochemistry. Recommendations 1974, Pure Appl. Chem., 1976, 45, 11-30
^Nomenclature of organic chemistry, section F: natural products and related compounds. Recommendations 1976, Eur. J. Biochem., 1978, 86, 1-8
^Nomenclature of organic chemistry, section H: isotopically modified compounds. Recommendations 1977, Eur. J. Biochem., 1978, 86, 9-25; 1979, 102, 315-316; Pure Appl. Chem., 1979, 51, 353-380
^Revision of the extended Hantzsch-Widman system of nomenclature for heteromonocycles. Recommendations 1982, Pure Appl. Chem., 1983, 55, 409-416.
^Treatment of variable valence in organic nomenclature (lambda convention). Recommendations 1983, Pure Appl. Chem., 1984, 56, 769-778
^Extension of rules A-1.1 and A-2.5 concerning numerical term used in organic chemical nomenclature. Recommendations 1986, Pure Appl. Chem., 1986, 58, 1693-1696 [numerical terms to 9999]。
^Nomenclature for cyclic organic compounds with formal contiguous double bonds (the δ-convention). Recommendations 1988, Pure Appl. Chem., 1988, 60, 1395-1401.
^Revised nomenclature for radicals, ions, radical ions and related species. Pure Appl. Chem., 65, 1993, 1357-1455
^Glossary of class names of organic compounds and reactive intermediates based on structure. Recommendations 1995, Pure Appl. Chem., 67, 1995, 1307-1375.
^Basic Terminology of Stereochemistry. IUPAC recommendations 1996, Pure Appl. Chem., 68, 1996, 2193-2222.
^Nomenclature of Fused and Bridged Fused Ring Systems. IUPAC Recommendations 1998, Pure Appl. Chem., 1998, 70, 143-216.
^Phane Nomenclature. Part I: Phane Parent Names. IUPAC Recommendations 1998, Pure Appl. Chem., 1998, 70, 1513-1545.
^Extension and Revision of the von Baeyer System for Naming Polycyclic Compounds (Including Bicyclic Compounds). IUPAC Recommendations 1999, Pure Appl. Chem., 1999, 71, 513-529.
^Extension and Revision of the Nomenclature for Spiro Compounds. IUPAC Recommendations 1999, Pure Appl. Chem., 1999, 71, 531-558.
^Revised Section F: Natural products and related compounds. IUPAC Recommendations 1999, Pure Appl. Chem., 1999, 71, 587-643.
^Nomenclature for the C60-Ih and C70-D5h(6) Fullerenes. IUPAC Recommendations 2002, Pure Appl. Chem., 2002, 74, 629-695.
^Phane nomenclature. Part II. Modification of the degree of hydrogenation and substitution derivatives of phane parent hydrides. IUPAC Recommendations 2002, Pure Appl. Chem., 2002, 74, 809-834.
^Numbering of Fullerenes. IUPAC Recommendations 2004. Pure Appl. Chem., 2005, 77, 843-923.
外部链接
InteractiveIUPAC Compendium of Chemical Terminology(interactive "Gold Book")
IUPAC Nomenclature Books Series(list of all IUPAC nomenclature books, and means of accessing them)
IUPAC Compendium of Chemical Terminology("Gold Book")
Quantities, Units and Symbols in Physical Chemistry("Green Book")
IUPAC Nomenclature of Organic Chemistry("Blue Book")
Nomenclature of Inorganic Chemistry IUPAC Recommendations 2005("Red Book")
IUPAC Recommendations on Organic & Biochemical Nomenclature, Symbols, Terminology, etc.(includes IUBMB Recommendations for biochemistry)
chemicalize.orgA free web site/service that extracts IUPAC names from web pages and annotates a "chemicalized" version with structure images. Structures from annotated pages can also be searched.
ChemAxon Name Structure– IUPAC (& traditional) name to structure and structure to IUPAC name software. As used atchemicalize.org
ACD/Name– Generates IUPAC, INDEX (CAS), InChi, Smiles, etc. for drawn structures in 10 languages and translates names to structures. Also available as batch tool and for Pipeline Pilot. Part ofI-Lab 2.0
法芬
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