Total Synthesis of Thymine Polyoxin C

DOI: 10.1016/S0040-4039(00)78564-9

Source and publish data:

Tetrahedron Letters p. 9439 - 9442 (1994)

Update date:2022-09-26

Topics:

Authors:

Dondoni, Alessandro

Junquera, Federico

Merchan, Francisco L.

Merino, Pedro

Tejero, Tomas

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Article abstract of DOI:10.1016/S0040-4039(00)78564-9

An expeditious synthesis of thymine polyoxin C in 6 steps (7.2 percent overall yield) based on the stereocontrolled addition of 2-lithiofuran, a masked carboxylate group, to the N-benzyl nitrone derived from methyl 2,3-O-isopropylidene-dialdo-D-ribofurano

Full text of DOI:10.1016/S0040-4039(00)78564-9

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Product name:Methyl 5-amino-1,5-dideoxy-1-(3,4-dihydro-5-methyl-2,4-dioxo-1(2H)-pyrimidinyl)-β-D-allofuranuronate 2,3-diacetate

Cas No:127257-35-6

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