Synthesis of the Enantiomers of Some Methyl-branched Cuticular Hydrocarbons of the Ant, Diacamma sp.
-
- MARUKAWA Kaoru
- Department of Chemistry, Faculty of Science, Science University of Tokyo
-
- TAKIKAWA Hirosato
- Department of Chemistry, Faculty of Science, Science University of Tokyo
-
- MORI Kenji
- Department of Chemistry, Faculty of Science, Science University of Tokyo
Search this article
Description
The enantiomers of 3-methylpentacosane, 3-methylheptacosane, 3-methylnonacosane, 13-methylheptacosane, and 5-methylheptacosane were synthesized by starting from the enantiomers of 2-methylbutyl bromide or citronellol. These methyl-branched alkanes are the characteristic components of the cuticular hydrocarbons of queen of the ant, Diacamma sp.
Journal
-
- Bioscience, Biotechnology, and Biochemistry
-
Bioscience, Biotechnology, and Biochemistry 65 (2), 305-314, 2001
Japan Society for Bioscience, Biotechnology, and Agrochemistry
- Tweet
Keywords
Details 詳細情報について
-
- CRID
- 1390001206475568640
-
- NII Article ID
- 110002680258
-
- NII Book ID
- AA10824164
-
- COI
- 1:CAS:528:DC%2BD3MXhslKgtL4%3D
-
- ISSN
- 13476947
- 09168451
-
- NDL BIB ID
- 5696742
-
- PubMed
- 11302163
-
- Text Lang
- en
-
- Article Type
- journal article
-
- Data Source
-
- JaLC
- NDL Search
- Crossref
- PubMed
- CiNii Articles
- OpenAIRE
-
- Abstract License Flag
- Disallowed