The Action of some Isoquinoline Derivatives
نویسندگان
چکیده
منابع مشابه
Acid-base interactions in some isoquinoline and quinazoline amino derivatives
Few groups of substituted 1-aminoisoquinoline, 4-aminoand 2,4-diaminoquinazoline derivatives have been examined in order to find general relationships between the basicity and a kind of substituent. pKa Values have been determined for these compounds and correlated with the original Hammett σm and σp constants. They clearly showed that the steric effects of the bulky substituents neighbouring t...
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Early types of antibacterial substances were not specifically antibacterial, but were usually toxic to all living cells, and were of value only in so far as they could be employed without serious damage to the host. The search for more suitable antibacterial agents resulted in the preparation and testing of many substances of widely different constitution, and it was from the empirical yet syst...
متن کاملThe cyclization reaction of ortho-ethynylbenzaldehyde derivatives into isoquinoline derivatives.
In order to elucidate the reaction mechanism of the cyclization between an ethynyl group and an imino group at the ortho-position on an aromatic ring to afford isoquinolines, reaction of 2-ethynylbenzaldehydes under various conditions was examined. It is concluded that reaction proceeds via an ionic process and the isoquinoline 4-hydrogen atom derives from the solvent. In addition, it was found...
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توسیع تعدادی از نامساوی های چند جمله ای در مشتق قطبی
15 صفحه اولThe lipotropic action of some halogen derivatives of acetic acid.
Hawk, P. B., Oser, L. B. & Summerson, W. H. (1947). Practical Phyiological Chemi8try, 12th ed., p. 1273. London: J. and A. Churchill Ltd. Koszewski, B. J. (1952). Blood, 7, 1182. Leaf, G. & Neuberger, A. (1947). Biochem. J. 41, 280. Lindon, 0. & Work, E. (1953). Biochem. J. 55, 554. Nath, M. C. & Behki, R. M. (1958). Arch. Biochem. Biophy8. 73, 65. Nath, M. C., Chitale, R. P. & Belavady, B. (19...
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ژورنال
عنوان ژورنال: Biochemical Journal
سال: 1911
ISSN: 0306-3283
DOI: 10.1042/bj0050243