Synthesis of 2-fluoroabscisic acid: A potential photo-stable abscisic acid
摘要:
Novel fluorinated abscisic acid (ABA) analogs were synthesized by introducing fluorine through the Wittig reaction of alpha-ionone derivatives with triethyl phosphono-2-fluoroacetate. Molecular orbital calculations showed that the introduction of fluorine at the 2 position stabilized the configuration of the side chain. (C) 1997 Elsevier Science Ltd.
Synthesis of 2-fluoroabscisic acid: A potential photo-stable abscisic acid
摘要:
Novel fluorinated abscisic acid (ABA) analogs were synthesized by introducing fluorine through the Wittig reaction of alpha-ionone derivatives with triethyl phosphono-2-fluoroacetate. Molecular orbital calculations showed that the introduction of fluorine at the 2 position stabilized the configuration of the side chain. (C) 1997 Elsevier Science Ltd.
Synthesis of 2-fluoroabscisic acid: A potential photo-stable abscisic acid
作者:Bum Tae Kim、Yong Ki Min、Tadao Asami、No Kyun Park、Oh Young Kwon、Kwang Yun Cho、Shigeo Yoshida
DOI:10.1016/s0040-4039(97)00172-x
日期:1997.3
Novel fluorinated abscisic acid (ABA) analogs were synthesized by introducing fluorine through the Wittig reaction of alpha-ionone derivatives with triethyl phosphono-2-fluoroacetate. Molecular orbital calculations showed that the introduction of fluorine at the 2 position stabilized the configuration of the side chain. (C) 1997 Elsevier Science Ltd.