## Abstract – Die Kondensation von D, L‐2,3‐O‐Isopropyliden‐4‐methyl‐erythrulose mit 2,4,5‐Triamino‐6‐hydroxypyrimidin wird beschrieben. Die Luft‐Oxydation des hydrierten Kondensationsproduktes führt zu D, L‐1′,2′‐O‐Isopropyliden‐biopterin ohne Abspaltung der Seitenkette. Durch hydrolytische Abspal
Über Pterinchemie. 60. vorläufige Mitteilung [1]. Eine neue, regiospezifische Synthese von L-Biopterin
✍ Scribed by Bernhard Schircks; Jost H. Bieri; Max Viscontini
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- German
- Weight
- 178 KB
- Volume
- 60
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
A new, regiospecific synthesis of L‐biopterine
Pure L‐biopterine (I) is obtained in 35–40% yield by condensation of 5‐desoxy‐L‐arabinose‐hydrazone acetate with 2,4,5‐triamino‐6‐hydroxy‐pyrimidine, followed by oxidation of the formed tetrahydro‐derivative and deacetylation of the L‐bioterine diacetate. Catalytic reduction of the L‐biopterine gives the expected mixture of two diastereomeric tetrahydro‐L‐biopterines.
📜 SIMILAR VOLUMES
**A Convenient Synthesis of Leucovorin** The synthesis of leucovorin, a 5‐formyl‐(6__R__ or __S__)‐5,6,7,8‐tetrahydropteroyl‐L‐glutamic acid (II) is described. The L‐folic acid was first reduced to (6__R__, __S__)‐tetrahy‐dro‐L‐folic acid (I); formylation with methyl‐formate in DMSO gave directly l