α-D-Ribofuranosyl 1,2-Cyclic Monophosphate. Isolation, NMR Spectroscopic Properties, and Rates and Mechanism of Acid and Alkaline Hydrolysis

DOI: 10.1021/jo00372a008

Source and publish data:

Journal of Organic Chemistry p. 4143 - 4146 (1986)

Update date:2022-08-16

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Authors:

Fathi, Reza

Jordan, Frank

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Article abstract of DOI:10.1021/jo00372a008

The five-membered ring cyclic phosphate α-D-ribofuranosyl 1,2-cyclic phosphate has been synthesized, isolated, and characterized both spectroscopically and with respect to acid and alkaline lability.The 31P NMR chemical shift (17 ppm downfield from intern

Full text of DOI:10.1021/jo00372a008

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