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• W3116724640 startingPage "531" @default.
• W3116724640 abstract "Monoacylation of symmetrical diamine is achieved when the primary α,ω-diamines (carbon numbers n = 3, 5 and 12) are diluted in ethyl acetate, and the resultant mixture is electrosprayed across a 10 mm distance in ambient air toward a mass spectrometer. The N-acylated product is formed in charged microdroplets without acidifying and activating agents and in the absence of heat. This result provided an insight into the orientation of the amines in the droplets, suggesting that the ester is activated to react with the amine at the droplet surface due to the high abundance of protons at the air–droplet interface." @default.
• W3116724640 created "2021-01-05" @default.
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• W3116724640 date "2020-12-28" @default.
• W3116724640 modified "2023-10-02" @default.
• W3116724640 title "Monoacylation of Symmetrical Diamines in Charge Microdroplets" @default.
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• W3116724640 doi "https://doi.org/10.1021/jasms.0c00384" @default.
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