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- W3013921922 abstract "With a view to make conveniently labeled mass spectrometry standards available, a set of deuterated sphingomyelins were prepared by a new expedient, flexible, robust, scalable, and high-yielding synthetic scheme starting from 2-azido-3-O-benzoylsphingosine as the key intermediate. Unlike previously published procedures, this work emphasizes the benefit arising from the choice of the azido function as a masking group for the reactive primary amine during the troublesome, though crucial, phosphorylation step." @default.
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- W3013921922 date "2020-03-24" @default.
- W3013921922 modified "2023-10-11" @default.
- W3013921922 title "An Improved, Versatile, and Easily Scalable Synthesis of Sphingomyelins: Application to Stable Isotope Labeling" @default.
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- W3013921922 doi "https://doi.org/10.1055/s-0039-1690863" @default.
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