Nucleosidic enol esters: A versatile tool for the synthesis of 3'-carbon-substituted nucleosides

DOI: 10.1016/S0040-4039(00)74884-2

Source and publish data:

Tetrahedron Letters p. 777 - 780 (1991)

Update date:2022-08-04

Topics:

Authors:

Haraguchi

Tanaka Tanaka

Itoh Itoh

Miyasaka

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Article abstract of DOI:10.1016/S0040-4039(00)74884-2

Enol esters of uracil and adenine nucleosides prepared by selenoxide fragmentation of the corresponding 3'-phenylseleno derivatives have been shown to yield 3'-carbon-substituted products upon reacting with MeLi followed by electrophiles, providing the fi

Full text of DOI:10.1016/S0040-4039(00)74884-2

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