✦ LIBER ✦

Investigation into the tuberculostatic activity of some derivatives of p. aminobenzoic acid

✍ Scribed by C. van der Stelt; A. J. Zwart Voorspuij; W. Th. Nauta

Book ID: 110551290
Publisher: Springer Netherlands
Year: 1954
Tongue: English
Weight: 562 KB
Volume: 20
Category: Article
ISSN: 0003-6072
DOI: 10.1007/bf02543731

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Investigation into the tuberculostatic a

Investigation into the tuberculostatic activity of some aromatic hydroxy compounds

✍ J. Gootjes; A. J. Zwart Voorspuij; W. Th. Nauta 📂 Article 📅 1953 🏛 Springer Netherlands 🌐 English ⚖ 289 KB

X-ray crystallographic investigation of

X-ray crystallographic investigation of the complexes of p-aminobenzoic acid with metals

✍ I. R. Amiraslanov; Kh. S. Mamedov; É. M. Movsumov; F. N. Musaev; G. N. Nadzhafov 📂 Article 📅 1980 🏛 SP MAIK Nauka/Interperiodica 🌐 English ⚖ 423 KB

Derivatives of p-aminobenzoic acid and t

Derivatives of p-aminobenzoic acid and their action on the growth of bacteria

✍ J. L. Sirks 📂 Article 📅 1953 🏛 Springer Netherlands 🌐 English ⚖ 181 KB

Investigation of the antitumor activity

Investigation of the antitumor activity of podocarpic acid derivatives

✍ Edward J. Parish; D. Howard Miles 📂 Article 📅 1984 🏛 John Wiley and Sons 🌐 English ⚖ 306 KB

ChemInform Abstract: Synthesis, Antithro

ChemInform Abstract: Synthesis, Antithrombin and Tuberculostatic Activity of 2-Hydrazino Derivatives of Acylpyruvic Acid Methyl Esters.

✍ S. Yu. Solodnikov; G. D. Mails; O. P. Krasnykh; E. A. Gun; S. A. Naser; N. A. Ko 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB 👁 1 views

Investigations on pyrazine derivatives.

Investigations on pyrazine derivatives. VII: On the conversion of pyrazine 2,5-dicarboxylic acid into some derivatives of 2-aminopyrazine 5-carboxylic acid

✍ W. J. Schut; H. I. X. Mager; W. Berends 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 445 KB

## Abstract Pyrazine 2,5‐dicarboxylic acid was prepared by oxidation of 2,5‐dimethylpyrazine with selenium dioxide. 2,5‐Diethoxycarbonylpyrazine appeared to be a suitable starting‐material for the preparation of monocarbamoyl‐ and monocarboxyhydrazide derivatives. Hofmann degradation of 2‐carbamoyl