Model studies related to the cofactor of the oxomolybdoenzymes. Part 5. Synthesis of 6-alkenyl- and 6-alkynylpterins

DOI: 10.1016/S0040-4039(00)92091-4

Source and publish data:

Tetrahedron Letters p. 3371 - 3374 (1992)

Update date:2022-08-02

Topics:

Authors:

Russell Russell

Garner Garner

Joule Joule

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Article abstract of DOI:10.1016/S0040-4039(00)92091-4

6-Alkenylpterin (6) was prepared from pteridine (3a) and (R)-glyceraldehyde acetonide via Wittig condensation. Treatment of 6 with bromine and then diazabicycloundecane (DBU) produced the corresponding alkyne (8)

Full text of DOI:10.1016/S0040-4039(00)92091-4

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Product name:Methanesulfonate[2-(2,2-dimethyl-propionylamino)-4-oxo-3,4-dihydro-pteridin-6-ylmethyl]-triphenyl-phosphonium;

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