Alkaloids of the Australian Apocynaceae: Kopsia longiflora Merr. III. Preliminary Degradation of the Alkaloids

1962 ◽  
Vol 15 (1) ◽  
pp. 130 ◽  
Author(s):  
WD Crow ◽  
M Michael

Graded alkaline hydrolysis of the monoacid tertiary bases kopsiflorine (C23H28O5N2), kopsilongine (C24H30O6N2), and kopsamine (C24H28O7N2) shows that they contain two methoxycarbonyl groups. All but one of the residual oxygen atoms are accounted for as aromatic ether linkages. One of the methoxycarbonyl groups is responsible for the deactivation of the other nitrogen atom (N(a)) present, since anew basic centre is generated by partial hydrolysis and subsequent decarboxylation of the acid produced. The alkaloids are tentatively formulated as blocked indoline bases containing a urethane grouping at N(a). The fourth alkaloid, kopsinine (C21H26O2N2) is similarly formulated, but in this case N(a) is weakly basic, the urethane methoxycarbonyl group and the additional oxygen atom being absent.

1956 ◽  
Vol 34 (3) ◽  
pp. 338-344 ◽  
Author(s):  
E. L. Falconer ◽  
G. A. Adams

Partial hydrolysis of hemicellulose B from oat hulls yielded two aldobiouronic acids, which were identified as 2-O-(4-O-methyl-α-D-glucopyruronosyl)-D-xylose and 2-O-(α-D-glucopyruronosyl)-D-xylose respectively. In addition, two aldotriouronic acids were isolated, one yielding on hydrolysis xylose and 4-O-methyl-glucuronic acid, and the other, xylose, galactose, and glucurone.


1984 ◽  
Vol 49 (8) ◽  
pp. 1780-1787 ◽  
Author(s):  
Štefan Kučár ◽  
Juraj Zámocký ◽  
Juraj Zemek ◽  
Dušan Anderle ◽  
Mária Matulová

Partial hydrolysis of per-O-acetyl- and per-O-benzoyl derivatives of 1,6-anhydro-β-D-glucopyranose with methanolic hydrogen chloride and hydrazine hydrate was investigated. The acyl group at C(3) is of substantial influence on the course of hydrolysis. The esterified hydroxyl group at C(3) was found to be most stable on acid hydrolysis with methanolic hydrogen chloride when compared with that at C(2), or C(4); on the other hand, this ester group is the most labile upon hydrolysis with hydrazine hydrate. Selectivity of the respective ester groups towards hydrolysis made it possible to prepare all variations of acetyl and benzoyl derivatives of 1,6-anhydro-β-D-glucopyranose.


The kinetics of the reaction of methyl fluoride with water and the hydroxyl ion have been determined experimentally at various concentrations and temperatures. The results are compared with the data available on the other methyl halides. The mechanism of the anionic reaction is discussed in terms of a hypothesis according to which the rate-determining step is the partial desolvation of the ion. This mechanism is extended to account also for the kinetic features of the hydrolysis.


Valency implies the existence of something equivalent to the possession by an atom of points of attachment, and is inseparable from the idea of chemical combination; but it must not be confused, as has often been done, with the force acting at those points. The properties of a mass of matter are the sum of those of its constituents, and, since molecules combine together, the affinities and valencies effecting their union must be those of the constituent atoms. The satisfaction of such additional valencies will represent a comparatively small expenditure of energy, for, even when principal valencies are concerned, as when an element forms pairs of oxides or halides, the heat evolution on combining with the additional oxygen atom is, on the average, only 38 per cent. of what it is on combining with the first atom or atoms (17 cases), and 52 per cent. in the case of the halides (10 cases). At this rate residual affinity must soon become reduced to a quantity insufficient for the attachment of another free atom, but might still be sufficient to unite with it if it were already in combination, and had only its own residual affinity available. Platinum is hexavalent in Cl 4 Pt ClK ClK , though Cl 6 Pt cannot exist. It is, therefore, only in so-called molecular compounds that the highest valencies of an atom can be expected, though no fundamental differences can be imagined between the higher and the principal valencies; this is admitted even by those who have coined a distinctive name for the higher valencies ( e. g. , Werner’s “co-ordination values”). The general rule that additional valencies come into existence in pairs is not invalidated by certain apparent exceptions. Thus, the most stable arrangement of five atoms round a central one is two in one plane, and three in the plane at right angles; according as the positions occupied are those in the one, the other, or both planes, the atom will show valencies of 2, 3 or 5, and by the suppression or development of pairs of valencies, other values of 1, 4, 7, 9, etc., might be shown.


2006 ◽  
Vol 61 (11) ◽  
pp. 1327-1334 ◽  
Author(s):  
Ralph Puchta ◽  
Michael Galle ◽  
Nico J. R. van Eikema Hommes

DFT-calculations (RB3LYP/LANL2DZp) show that the migration of a proton inside [1.1.1]- and [2.2.2]-cryptand from one nitrogen atom to the other follows different paths. While the proton in [H⊂1.1.1]-cryptand moves via an ether oxygen atom (activation energy: 19.2 kcal/mol), the proton in [H⊂2.2.2]-cryptand moves directly from one nitrogenatom to the other (activation energy: 16.1 kcal/mol). Our calculations rule out the application of doubly protonated [2.2.2]-cryptands as anion hosts.


1981 ◽  
Vol 46 (3) ◽  
pp. 597-606 ◽  
Author(s):  
Karel Šindelář ◽  
Jiří Holubek ◽  
Jan Metyš ◽  
Marie Bartošová ◽  
Miroslav Protiva

Reactions of potassium salts of 2-methoxy-, 2-ethoxy- and 2-benzyloxyphenol with 2-methyl-3-dimethylaminopropyl chloride and 3-dimethylamino-2phenylpropyl chloride in boiling 2-butanone in the presence of potassium iodide gave the title compounds IV-VI which were partially demethylated by treatment with ethyl chloroformate in boiling benzene and by the following alkaline hydrolysis of the crude intermediates. In series a (3-aryloxy-2-methylpropylamines) the demethylation proceeded normally under the formation of the methylamino compounds VIIa-IXa; in series b (3-aryloxy-2-phenylpropylamines), however, the treatment with ethyl chloroformate effected a double cleavage resulting, after the alkaline hydrolysis, in N-methyl-2-phenylallylamine (XIII).The pharmacological testing did not confirm the expected thymoleptic effects of the compounds (IVa, VIIa); on the other hand, the benzyl ethers IXa and especially VIb exhibited strong antiarrhythmic activity.


1988 ◽  
Vol 66 (3) ◽  
pp. 517-527 ◽  
Author(s):  
Antonio Delgado ◽  
José Miguel Garcia ◽  
David Mauleon ◽  
Cristina Minguillon ◽  
Joan Ramon Subirats ◽  
...  

Synthesis and conformational analysis of several cis- and (or) trans-2-amino-1,2,3,4-tetrahydro-1-naphthalenols are described. Introduction of the nitrogen atom at the C(2) position of the starting tetralones 3 has been carried out through nitrosation followed by reduction of the intermediate hydroxyimino tetralone and (or) Neber rearrangement of the tosyloxy derivatives 7a–e. Stereoselective reduction of the C(1) carbonyl group of acetamidotetralones 5a–e or aminotetralones 8a–e afforded the corresponding acetamido or aminotetralols, respectively, of OH/N trans stereochemistry whereas an opposite stereoselectivity was observed in reduction of C(8)-OCH3 derivatives 5f and 8f under the same experimental conditions. Finally, acid hydrolysis of trans-acetamidotetralols led to cis-aminoalcohols in high yields. Conformational analysis has been carried out by 1H nuclear magnetic resonance techniques and MM2 theoretical calculations. All cis derivatives showed a major conformation in which the C(1)-OH group adopts a pseudoaxial disposition. On the other hand, trans-aminoalcohols in CDCl3 showed a major or exclusive OH/N trans-dipseudoequatorial conformation in which stabilization by intramolecular OH/N hydrogen bonding is possible. The only exception was found in C(8)-OCH3trans-aminoalcohols in DMSO-d6 solution, which showed a major OH/N trans-diaxial conformation.


1953 ◽  
Vol 31 (9) ◽  
pp. 814-820 ◽  
Author(s):  
R. U. Lemieux ◽  
H. F. Bauer

Periodate oxidation of any one mono-O-methylglucopyranose and alkaline hydrolysis of the product yields a substance which can be positively distinguished by paper chromatography from the products formed under the same conditions from the other mono-O-methylglucopyranoses. Thus, the components of a mixture of the mono-O-methylglucopyranoses can be readily identified. The method appears useful for the identification of di-O-methylglucoses. Reduction with sodium borohydride prior to periodate oxidation renders the method useful for the identification of tri-O-methylglucoses. The potential value of the method, which can be used on a microscale, is illustrated by an application to the characterization of the O-methylglucoses derived from a water-soluble O-methyl-cellulose


TAPPI Journal ◽  
2015 ◽  
Vol 14 (4) ◽  
pp. 237-244 ◽  
Author(s):  
JONI LEHTO ◽  
RAIMO ALÉN

Untreated and hot water-treated birch (Betula pendula) sawdust were cooked by the oxygen-alkali method under the same cooking conditions (temperature = 170°C, liquor-to-wood ratio = 5 L/kg, and 19% sodium hydroxide charge on the ovendry sawdust). The pretreatment of feedstock clearly facilitated delignification. After a cooking time of 90 min, the kappa numbers were 47.6 for the untreated birch and 10.3 for the hot water-treated birch. Additionally, the amounts of hydroxy acids in black liquors based on the pretreated sawdust were higher (19.5-22.5g/L) than those in the untreated sawdust black liquors (14.8-15.5 g/L). In contrast, in the former case, the amounts of acetic acid were lower in the pretreated sawdust (13.3-14.8 g/L vs. 16.9-19.1 g/L) because the partial hydrolysis of the acetyl groups in xylan already took place during the hot water extraction of feedstock. The sulfur-free fractions in the pretreatment hydrolysates (mainly carbohydrates and acetic acid) and in black liquors (mainly lignin and aliphatic carboxylic acids) were considered as attractive novel byproducts of chemical pulping.


Sign in / Sign up

Export Citation Format

Share Document