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• W2901345747 abstract "The [4π + 2π] cycloaddition of methyl 3-(1,3-butadien-1/2-yl)pyropheophorbides-a with tetracyanoethylene, dimethyl acetylenedicarboxylate, and naphthoquinone gave the corresponding Diels–Alder reaction adducts. The trans-1-substituted 1,3-butadiene was more reactive than its regioisomeric 2-substituent. The oxidation of some cycloadducts gave C3-arylated chlorophyll derivatives, whose ortho-substitution blue-shifted the corresponding Qy absorption maxima in dichloromethane because of the steric repulsion between the aryl and chlorin π-planes." @default.
• W2901345747 created "2018-11-29" @default.
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• W2901345747 date "2019-01-01" @default.
• W2901345747 modified "2023-09-25" @default.
• W2901345747 title "Diels–Alder reactions of directly C3-dieneylated chlorophyll derivatives" @default.
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• W2901345747 doi "https://doi.org/10.1016/j.tetlet.2018.11.057" @default.
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