Difference between revisions of "Nomenclature of polycyclic compounds"

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*[[fusion nomenclature]]<ref name="fusion">{{IUPAC fused rings 1998}}.</ref>
 
*[[fusion nomenclature]]<ref name="fusion">{{IUPAC fused rings 1998}}.</ref>
 
*[[Nomenclature of natural products|natural product nomenclature]],<ref>{{IUPAC natural products 1999}}.</ref> which can be further subdivided into
 
*[[Nomenclature of natural products|natural product nomenclature]],<ref>{{IUPAC natural products 1999}}.</ref> which can be further subdivided into
**[[Nomenclature of steroids|steroid nomenclature]]
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**[[Nomenclature of steroids|steroid nomenclature]]<ref>{{IUPAC-IUB steroids 1989}}.</ref>
 
**[[Nomenclature of terpenes|terpene nomenclature]]
 
**[[Nomenclature of terpenes|terpene nomenclature]]
 
**[[Nomenclature of alkaloids|alkaloid nomenclature]]
 
**[[Nomenclature of alkaloids|alkaloid nomenclature]]
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==References==
 
==References==
 
{{reflist}}
 
{{reflist}}
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[[Category:Chemical nomenclature|Polycyclic compounds]]
  
 
{{CC-BY-3.0}}
 
{{CC-BY-3.0}}

Latest revision as of 06:32, 21 November 2009

The nomenclature of polycyclic compounds is a specialised area of organic nomenclature. There are several methods, depending on the particular compound:

While there may be choice of nomenclature methods for a given compound, it is normal to use natural product nomenclature for steroids, terpenes, alkaloids and other compounds of biological origin; fusion nomenclature for fused ring systems such as polycyclic aromatic hydrocarbons; and von Baeyer nomenclature for other polycyclic compounds. The systems are not completely independent of one another.

Definitions

Polycyclic compound

A compound which, for nomenclature purposes, requires at least two scissions to convert it into an open-chain compound.[1]

Spiro compound

A compound which has two (or three) rings which have only one atom in common and the two (or three) rings are not linked by a bridge. The common atom is known as a spiro atom.[2]

Fusion

The process of joining rings, for nomenclature purposes, so that two rings have two atoms and one bond in common, the resulting compound being regarded as being derived from the two rings as separate entities.[3]

References

  1. 1.0 1.1 Extension and Revision of the von Baeyer System for naming Polycyclic Compounds (including Bicyclic Compounds) (IUPAC Recommendations 1999). Pure Appl. Chem., 71 (3), 513–29. DOI: 10.1351/pac199971030513.
  2. 2.0 2.1 Extension and Revision of the Nomenclature for Spiro Compounds (IUPAC Recommendations 1999). Pure Appl. Chem. 1999, 71 (3), 531–58. DOI: 10.1351/pac199971030531.
  3. 3.0 3.1 Nomenclature of Fused and Bridged Fused Ring Systems (IUPAC Recommendations 1998). Pure Appl. Chem., 70 (1), 143–216. DOI: 10.1351/pac199870010143.
  4. Revised Section F: Natural Products and Related Compounds (IUPAC Recommendations 1999). Pure Appl. Chem., 71 (4), 587–643. DOI: 10.1351/pac199971040587.
  5. Nomenclature of Steroids (IUPAC–IUB Recommendations 1989). Pure Appl. Chem., 61 (10), 1783–1822. DOI: 10.1351/pac198961101783.
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