Comparisons of various biological activities of stereoisomers of methyl jasmonate
β Scribed by Yasunori Koda; Yoshio Kikuta; Takeshi Kitahara; Tsunehiro Nishi; Kenji Mori
- Book ID
- 103339805
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- English
- Weight
- 930 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0031-9422
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Due to the presence of an asymmetrically substituted C atom, dimethenamid [2-chloro-N-(2,4-dimethyl-3-thienyl)-N-(2-methoxy-1-methylethyl)acetamide], a recently introduced N-thienyl chloroacetamide herbicide, exists as two stereoisomers (S and R) having di β ering herbicidal activities as demonstrate
## Abstract **BACKGOUND:** Loquat fruit is rich in natural antioxidants and has shown a remarkably high antioxidant activity. To search for an effective method for maintaining or even improving antioxidant activity during postharvest storage, we investigated the effect of 10 Β΅mol L^β1^ methyl jasmo