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Heilmittelchemische Studien in der heterocyclischen Reihe. 22. Mitteilung. Pyrazolo-pyrimidine II. Pyrazolo[3,4-d]pyrimidine mit Koffein-ähnlicher Struktur und Wirkung

✍ Scribed by P. Schmidt; K. Eichenberger; J. Druey


Publisher
John Wiley and Sons
Year
1958
Tongue
German
Weight
554 KB
Volume
41
Category
Article
ISSN
0018-019X

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✦ Synopsis


  1. Two mechanisms can be admitted for the reactivation of the succinatecytochrome-c reductase system. An earlier described reactivation of the extracted system by isoprene-like substances (vitamins E and K) is to be distinguished from an unspecific reactivation by Z-methyl-l,4-naphthoquinone, which is caused by the redox system.

  2. Ubiquinone, described by Morton, does not reactivate by its redox system but probably by its isoprene like-side chain.


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## Abstract The synthesis of 4‐ and 6‐substituted 1‐H‐ and 1‐phenyl‐pyrazolo‐(3,4‐d)‐pyrimidines is described. It starts from ethyl ethoxymethylene cyanoacetate from which the 4‐hydroxy‐pyrazolo‐(3,4‐d)‐ pyrimidines can be obtained in two steps through the corresponding 2‐substituted 3‐amino‐4‐carb

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✍ P. Schmidt; K. Eichenberger; M. Wilhelm 📂 Article 📅 1962 🏛 John Wiley and Sons 🌐 German ⚖ 483 KB

## Abstract Condensation of 3‐amino‐4‐carbethoxy‐pyrazoles with nitriles led to a new synthesis of 6‐C‐substituted pyrazolo[3,4‐d]pyrimidines and 6‐amino‐pyrazolo‐[3,4‐b]pyridines. The structure of the new derivatives was established by independent syntheses. The pyrazolo‐pyrimidines can be cleaved