Absolute configuration of a new mosquito repellent, (+)-eucamalol and the repellent activity of its epimer.

Article abstract of DOI:10.1271/bbb.59.1139

(+)-Eucamalol (1) and (-)-1-epi-eucamalol (2) were synthesized from (S)-(-)-perillaldehyde to determine the absolute configuration of 1, the structure of natural (+)-eucamalol being determined to be (1R,6R)-(+)-3-formyl-6-isopropyl-2-cyclohexen-1-ol. (+)-

Full text of DOI:10.1271/bbb.59.1139

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Absolute Configuration of a New Mosquito Repellent,
(+)-Eucamalol and the Repellent Activity of Its
Epimer
Atsushi Satoha, Hisashi Utamuraa, Teruhiko Nakadea & Hiroyuki Nishimuraa
a Department of Bioscience and Technology, School of Engineering, Hokkaido Tokai
University, Sapporo 005, Japan
Published online: 12 Jun 2014.
To cite this article: Atsushi Satoh, Hisashi Utamura, Teruhiko Nakade & Hiroyuki Nishimura (1995) Absolute Configuration
of a New Mosquito Repellent, (+)-Eucamalol and the Repellent Activity of Its Epimer, Bioscience, Biotechnology, and
Biochemistry, 59:6, 1139-1141, DOI: 10.1271/bbb.59.1139
To link to this article: http://dx.doi.org/10.1271/bbb.59.1139
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