Tricyclic "oxadiazaphosphorine oxide" guanosines a new strategy to functionalize guanosine at the exocyclic amino group

DOI: 10.1016/00404-0399(50)1395-X

Source and publish data:

Tetrahedron Letters p. 6651 - 6654 (1995)

Update date:2022-08-11

Topics:: Authors:

Guo, Yunkui

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Article abstract of DOI:10.1016/00404-0399(50)1395-X

A simple procedure is described for the preparation of modified guanosines via an oxidiazaphosphorine oxide guanosine derivative. This nucleoside has been successfully used in the synthesis of guanosine containing -(CH₂)₂OH, -(CH₂)₆NH₂, -NHNH₂ "handles", or a tethered acridine moiety at the 2-position.

Full text of DOI:10.1016/00404-0399(50)1395-X

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Article Doi

Tricyclic "oxadiazaphosphorine oxide" guanosines a new strategy to functionalize guanosine at the exocyclic amino group

DOI: 10.1016/00404-0399(50)1395-X

Source and publish data:

Authors:

Article abstract of DOI:10.1016/00404-0399(50)1395-X

Full text of DOI:10.1016/00404-0399(50)1395-X

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