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Efficient Synthesis of Long‐wavelength Absorbing Cyanochlorophyll a Derivatives via Stereoselective Horner–Wadsworth–Emmons Reaction

机译:通过立体选择霍尔 - 馄饨反应的高效合成氰基氯苯基衍生物的长波长衍生物

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In this article, we report the stereoselective Horner–Wadsworth–Emmons reaction of reactive carbonyl‐substituted chlorophyll a derivatives with diethyl cyanomethylphosphonate. We found that the formyl or keto group at the chlorin periphery can react stereoselectively with phosphonate carbanions to produce a series of cyanomethylene‐substituted chlorins with predominantly E geometry. Considering that no consistent records are available in the literature on the results of the allomerization of methyl pyropheophorbide a, we propose a reliable process for the transformation of this chlorophyll derivative. Our methodology represents a simple and efficient way for the preparation of novel, differently functionalized long‐wavelength absorbing chlorins, those can be applied for photodynamic therapy, solar cells, and other relevant purposes.
机译:在本文中,我们报告了活性羰基取代的叶绿素A衍生物与二乙基甲基甲基膦酸酯的立体选择性Horner-WADSworth-Emmons反应。我们发现氯环外周的甲甲基或酮基团可以用膦酸盐碳酸碳酸盐,以产生一系列的氰基甲基取代氯,主要是E几何形状。考虑到在文献中没有一致的记录,请参见甲基焦泡酰基甲醇A的激化的结果,我们提出了一种可靠的方法,用于转化该叶绿素衍生物。我们的方法代表了一种简单有效的方法,用于制备新颖的不同官能化的长波长吸收氯,可以应用于光动力治疗,太阳能电池和其他相关目的。

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