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- W2010489802 abstract "When kept at 105° for 2.5 h, weakly alkaline, syrupy d-erythrose was readily converted into a mixture containing mainly d-glycero-tetrulose, the previously unknown β-d-altro-l-glycero-3-octulofuranose (2), and α-d-gluco-l-glycero-3-octulopyranose, which were isolated as the corresponding acetates. Treatment of 2 with Dowex 50 (H+) resin yielded 3,8-anhydro-β-d-altro-l-glycero-octulopyranose, identified as its acetate. Previous discrepancies in the [α]d values for d-erythrose appear partly to originate in the self-aldol reaction. The dimerisation of d-erythrose 4-phosphate is also described." @default.
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- W2010489802 date "1981-03-01" @default.
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- W2010489802 title "Acid-catalysed re-arrangement of 2,4-0-ethylidene-d-erythrose" @default.
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- W2010489802 doi "https://doi.org/10.1016/s0008-6215(00)85260-x" @default.
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