Synthesis of New Abscisic Acid (ABA) Analogs Possessing a Geometrically Rigid Cyclized Side Chain
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概要
- 論文の詳細を見る
In a solution, cis-abscisic acid (ABA) isomerizes into the trans-isomer which is physiologically inactive, and this structural instability is regarded as a reason for insuitability of ABA in agricultural applications. The side chain of ABA, the 2-cis-4-trans-3-methyl-2,4-pentadienoic acid moiety, was replaced with various substituted phenyl groups to examine biological effects of the inflexibility of the part. Construction of the phenyl moiety was achieved by cyclizing the ionone derivatives and subsequent aromatization. Some of those new compounds showed ABA-like activity in both seed germination and transpiration assays.
- 社団法人日本農芸化学会の論文
- 1992-04-23
著者
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ASAMI Tadao
Riken
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Asami T
Dep. Of Applied Biological Chemistry Univ. Of Tokyo
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ASAMI Tadao
The Institute of Physical and Chemical Research (RIKEN)
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YOSHIDA Shigeo
The Institute of Physical and Chemical Research (RIKEN)
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MUROFUSHI Noboru
Department of Biotechnology, Akita Prefectural University
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Maejima Noboru
Department Of Biotechnology Akita Prefectural University
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Murofushi Noboru
Department Of Agricultural Chemistry The University Of Tokyo
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KIM Bum-Tae
Department of Agricultural Chemistry, The University of Tokyo
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MORITA Kensuke
Department of Agricultural Chemistry, The University of Tokyo
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SOH Chang-Ho
The Institute of Physical and Chemical Research (RIKEN)
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Soh C‐h
Inst. Physical And Chemical Research(riken) Saitama Jpn
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Morita K
Fukuoka Inst. Health And Environmental Sci. Fukuoka Jpn
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Kim Bum-tae
Department Of Agricultural Chemistry The University Of Tokyo
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Morita K
Univ. Tokyo Tokyo
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Asami Tadao
Riken Saitama Jpn
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