Abstract:
:The sex pheromone of the obscure mealybug, Pseudococcus viburni, consists of (1R*,2R*,3S*)-(2,3,4,4-tetramethylcyclopentyl)methyl acetate, the first example of a new monoterpenoid structural motif in which the two isoprene units forming the carbon skeleton are joined by 2'-2 and 3'-4 connections rather than the usual 1'-4, head-to-tail connections. This highly irregular terpenoid structure, and the irregular terpenoid structures of related mealybug species, suggest that these insects may have unique terpenoid biosynthetic pathways.
journal_name
J Chem Ecoljournal_title
Journal of chemical ecologyauthors
Millar JG,Midland SL,McElfresh JS,Daane KMdoi
10.1007/s10886-005-9320-0keywords:
subject
Has Abstractpub_date
2005-12-01 00:00:00pages
2999-3005issue
12eissn
0098-0331issn
1573-1561journal_volume
31pub_type
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