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- W2135890666 abstract "Not the carbon, nor the sulfur, but rather the hydrogen atom is the site of the attack of a mixture of a basic nucleophile and aqueous NaOH on neopentyl tresylate (1). The elimination–addition sequence is shown below. These observations strongly suggest that the structures assigned to affinity chromatography substrates derived from tresyl agarose should be revised." @default.
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- W2135890666 date "1995-08-18" @default.
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- W2135890666 title "Reactions of Neopentyl 2,2,2-Trifluoroethanesulfonate(Tresylate) with Nucleophiles: A Model Study for the Coupling of Nucleophiles with Tresyl Agarose" @default.
- W2135890666 doi "https://doi.org/10.1002/anie.199516121" @default.
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