Synthesis of all the stereoisomers of 6-methyl-2-octadecanone, 14-methyl-2-octadecanone, and 6,14-dimethyl-2-octadecanone, sex pheromone components of the Lyclene dharma dharma moth, from the enantiomers of citronellal.
- DOI
- 10.1271/bbb.120436
- Published
- 2012
- Container
- Bioscience, biotechnology, and biochemistry
- Publisher
- Not recorded
- Open access
- unknown
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BibTeX
@article{allodium:10.1271/bbb.120436,
title = {Synthesis of all the stereoisomers of 6-methyl-2-octadecanone, 14-methyl-2-octadecanone, and 6,14-dimethyl-2-octadecanone, sex pheromone components of the Lyclene dharma dharma moth, from the enantiomers of citronellal.},
author = {Shikichi Y and Mori K},
year = {2012},
journal = {Bioscience, biotechnology, and biochemistry},
doi = {10.1271/bbb.120436},
url = {https://doi.org/10.1271/bbb.120436}
}RIS
TY - JOUR TI - Synthesis of all the stereoisomers of 6-methyl-2-octadecanone, 14-methyl-2-octadecanone, and 6,14-dimethyl-2-octadecanone, sex pheromone components of the Lyclene dharma dharma moth, from the enantiomers of citronellal. AU - Shikichi Y AU - Mori K PY - 2012 JO - Bioscience, biotechnology, and biochemistry DO - 10.1271/bbb.120436 UR - https://doi.org/10.1271/bbb.120436 ER -
APA
Y, S., & K, M. (2012). Synthesis of all the stereoisomers of 6-methyl-2-octadecanone, 14-methyl-2-octadecanone, and 6,14-dimethyl-2-octadecanone, sex pheromone components of the Lyclene dharma dharma moth, from the enantiomers of citronellal.. Bioscience, biotechnology, and biochemistry. https://doi.org/10.1271/bbb.120436
Source records
- pubmed · retrieved 2026-09-27T08:43:01.971Z