Difference between revisions of "Diterpene"
Jump to navigation
Jump to search
m (Text replace - "== Authority ==" to "== Sources Checked for Data in Record ==") |
|||
Line 7: | Line 7: | ||
diterpenoid resin | diterpenoid resin | ||
− | == | + | ==Resources and Citations== |
− | + | * John S. Mills, Raymond White, ''The Organic Chemistry of Museum Objects'', Butterworth Heineman, London, 2nd ed., 1994, pp 85-92. | |
− | |||
− | |||
− | |||
− | * John S. Mills, Raymond White, ''The Organic Chemistry of Museum Objects'', Butterworth Heineman, London, 2nd ed., 1994 | ||
* ''Encyclopedia Britannica'', http://www.britannica.com Comment: "Chemical Compound." Encyclopædia Britannica. 2004. Encyclopædia Britannica Premium Service. 16 July 2004 . | * ''Encyclopedia Britannica'', http://www.britannica.com Comment: "Chemical Compound." Encyclopædia Britannica. 2004. Encyclopædia Britannica Premium Service. 16 July 2004 . |
Latest revision as of 13:19, 22 July 2022
Description
A chemical class of C20 hydrocarbon compounds that constitute the natural resins obtained from trees in the Coniferae and Leguminosae families. Cyclic diterpenes follow three basic structural types: Abietic acid, pimaric acid, and labdane (Mills and White 1994). Examples of natural resins formed from diterpenoid compounds: Rosin, Venice turpentine, Strasbourg turpentine, Canada balsam, Copaiba balsam, Sandarac, and Copal.
Synonyms and Related Terms
diterpenoid resin
Resources and Citations
- John S. Mills, Raymond White, The Organic Chemistry of Museum Objects, Butterworth Heineman, London, 2nd ed., 1994, pp 85-92.
- Encyclopedia Britannica, http://www.britannica.com Comment: "Chemical Compound." Encyclopædia Britannica. 2004. Encyclopædia Britannica Premium Service. 16 July 2004 .