| Literature DB >> 22246522 |
Nobuhiro Shimizu1, Ryota Yakumaru, Tomoyo Sakata, Satoshi Shimano, Yasumasa Kuwahara.
Abstract
The absolute configuration of the iridoid monoterpene chrysomelidial from the oribatid mite, Austrotritia dentate Aoki, was elucidated by the GC-MS and GC comparisons with four synthetic stereoisomers of this well-known natural product. This identification was made possible by asymmetric synthesis of the known alcohol, (5S,8S)-chrysomelidiol. The GC retention time of diol derived from the natural oribatid dial agreed with that of the synthetic (5S,8S)-chrysomelidiol, confirming that the absolute configurations at C5 and C8 positions of the natural chrysomelidial are both S. Chrysomelidial was detected as a single or a major component in nine oribatid mites examined; thus, this compound is considered to be commonly distributed in Oribotririidae where it serves a defensive role.Entities:
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Year: 2012 PMID: 22246522 DOI: 10.1007/s10886-012-0064-3
Source DB: PubMed Journal: J Chem Ecol ISSN: 0098-0331 Impact factor: 2.626