Stereochemical Structure-Activity Relationship of N-(2, 3-Epoxypropyl)-N-(α-methylbenzyl)benzenesulfonamide Derivatives
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概要
- 論文の詳細を見る
The absolute configurations of two asymmetric centers in four stereoisomers of N-(2, 3-epoxypropyl)-N-(a-methylbenzyl)benzenesulfonamide were determined and their biological activities were tested. Consequently, N-[(R)-2, 3-epoxypropyl]-N-[(R)-α-methylbenzyl]benzenesulfonamide was found to be the most active isomer and the stereochemistry of the benzyl position was found to be more important than that of C2 in the epoxypropyl group for biological activity.
- 社団法人 日本農芸化学会の論文
著者
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Yoneyama Koichi
Weed Sci. Center Utsunomiya Univ.
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Takematsu Tetsuo
Weed Control Research Institute Faculty Of Agriculture Utsunomiya University
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Konnai Makoto
Weed Control Research Institute Faculty Of Agriculture Utsunomiya University
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Ichizen Nobumasa
Weed Control Research Institute Faculty Of Agriculture Utsunomiya University
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JIKIHARA Tetsuo
Weed Control Research Institute, Faculty of Agriculture, Utsunomiya University
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USHINOHAMA Kazuyuki
Research Center, Mitsubishi Chemical Industries Ltd.
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YONEYAMA Koichi
Weed Control Research Institute, Faculty of Agriculture, Utsunomiya University
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