THE SYNTHESIS OF POSSIBLE DEGRADATION PRODUCTS OF METATHEBAINONE. I.

1944 ◽  
Vol 22b (3) ◽  
pp. 56-65 ◽  
Author(s):  
H. L. Holmes ◽  
L. W. Trevoy

The method of Crowley and Robinson (5) for the synthesis of 6-methoxy-3,4-dihydro-2-naphthoic acid has been modified to provide an improved and general method for the synthesis of 3,4-dihydro-2-naphthoic acids. The 7-methoxy-3,4-dihydro-2-naphthoic acid and its ethyl ester have been shown to react with butadiene and 2,3-dimethylbutadiene to give 3-methoxy-5,8,9,10,13,14-hexahydrophenanthrene-14-carboxylic acid and its 6,7-dimethyl derivative. The relationship of these hydrophenanthrenes to possible degradation products of morphine and metathebainone has been discussed. An unsuccessful attempt was made to lengthen the C14-chain by converting the carboxyl group to an aldehyde group by the Rosenmund method followed by condensation with malonic acid. The projected conversion failed in the first stage.

1998 ◽  
Vol 21 (4) ◽  
pp. 653-669 ◽  
Author(s):  
John E. Knight

The present paper is intended as a first step toward the establishment of a general theory of finitely subadditive outer measures. First, a general method for constructing a finitely subadditive outer measure and an associated finitely additive measure on any space is presented. This is followed by a discussion of the theory of inner measures, their construction, and the relationship of their properties to those of an associated finitely subadditive outer measure. In particular, the interconnections between the measurable sets determined by both the outer measure and its associated inner measure are examined. Finally, several applications of the general theory are given, with special attention being paid to various lattice related set functions.


HortScience ◽  
1992 ◽  
Vol 27 (6) ◽  
pp. 596g-597
Author(s):  
Claudinei Andreoli ◽  
Anwar A. Khan

The level of 1-aminocyclopropane-1-carboxylic acid (ACC) was 0.55 nmol.g-1 in dry lettuce (Lactuca sativa cv. Emperor) seeds. After 4h soak at 25°, 35° and 35°C+ KIN (kinetin, 50μM), the levels were 0, 0.2 and 1.14 nmol.g-1 seeds, respectively. The level of ACC was higher at 35°+KIN than at 35°C for up to 16h soak. No ACC was detectable at 25°C during 2 to 16h soak. In the presence of 50μM ABA, ACC level decreased to 0.2 nmol.g-1 at 4h soak and to zero level during 8 to 16h soak. The level of l-(malonylamino) cyclopropane-1-carboxylic acid (MACC), in dry seeds was 14 nmol.g-1. Exposure to 35°C in the presence or absence of KIN increased the level to 40-42 nmol.g-1 within 2h soaking, while at 25° only a slight increase (23 nmol.g-1) occurred. As in the case of ACC, the level of MACC was higher at 35°C+ KIN than at 35° or 25° for up to 16h soak.When seeds were soaked in ABA, the pattern of MACC produced was similar to that produced at 35°C. The results indicate that ACC synthase activity is enhanced by the addition of KIN at 35°C resulting in increased synthesis and/or accumulation of ACC and MACC. The relationship of ethylene biosynthesis to changes during stress imposition and alleviation by various factors will be discussed.


1977 ◽  
Vol 38 (04) ◽  
pp. 0809-0822 ◽  
Author(s):  
Laurence A. Sherman

SummaryAlthough the site and manner of normal catabolism of most of the fibrinogen pool is uncertain, certain pathways have been defined for various fibrinogen derivatives. Several organs, including the kidneys and reticuloendothelial system (RES) have been directly implicated as catabolic sites for various fibrinogen derivatives. The catabolic sites are not the same for different derivatives. These differences in catabolism are probably in part related to biochemical differences between fibrinogen and its various derivatives. Fibrinogen itself may be catabolized in endothelial cells, although little experimental data is available. RES uptake of intact fibrinogen does not occur, and removal of sialic acid does not result in the rapid hepatic uptake seen with other desialop rote ins. In contrast, a variety of studies have shown that fibrin is taken up by the RES by at least 2 mechanisms. The first is phagocytosis of microparticulate fibrin. The second involves a RES cell membrane binding of soluble fibrin which remains soluble in the blood, when complexed to fibrinogen or degradation products. Fibrinogen degradation products alone may in part also be cleared in the RES. Fragments D and E appear to be catabolized in the kidney, although both the intrarenal site of catabolism and the means of cellular uptake is unknown. It is clear that normally there is no urinary excretion of D and E. Another fibrinogen derivative, low molecular weight clottable fraction 1–8, is derived in vivo from intact fibrinogen. 1–8 is found normally in the blood and has a shorter t ½ than fibrinogen although much longer than D and E. While originally thought to be the result of limited plasmin degradation, 1–8 may be the result of another type of proteolysis. The sites of both 1–8 formation and degradation are unknown. Catabolism via fibrin, 1–8, or D and E appears to be only a small percent of normal turnover, albeit of much greater significance in disease. The relationship of these pathways to the as yet unknown catabolic site for the bulk of normal fibrinogen remains to be determined.


1948 ◽  
Vol 21 (1) ◽  
pp. 195-219 ◽  
Author(s):  
L. J. Bellamy ◽  
J. H. Lawrie ◽  
E. W. S. Press

Abstract The work is still in a preliminary stage, but sufficient has now been done to demonstrate the applicability of chromatographic methods to rubber analysis. The acetone extracts of vulcanizates are complex mixtures not readily amenable to analysis by normal chemical methods. By the use of this elegant technique, however, it has been possible to effect the efficient separation of wax, fat acids, accelerators, and antioxidants, not only from each other but also from naturally occurring coloring matter and from degradation products. The subsequent identification of the main fractions is then a relatively simple matter, as tests such as the cobalt oleate reaction for accelerators and the spot reactions for antioxidants can be applied without interference from any other components. The elegance of the method is further demonstrated by the fact that it can be used in the identification of components present in much smaller quantities than are detectable by other chemical methods. The accelerators and antioxidants studied so far are rather limited in number, but cover the main classes of these materials, and the method should, therefore, be applicable to the analysis of a number of technical vulcanizates, and the authors have, in fact, already made use of it with some success for this purpose. It is noteworthy that the adsorption and elution processes are quantitative, and that the whole of the material put on to a column can, therefore, be recovered from the various fractions. This, therefore, offers the possibility of quantitative work on such problems as the rate of consumption of accelerators during cure or the relationship of antioxidant content to behavior on aging. Such work would necessarily be restricted to experiments using pure accelerators and pure antioxidants which are single chemical entities. In this connection the degradation products obtained from mixes accelerated with T.M.T. or M.B.T.S. or D.P.G. are of interest both in the actual isolation of the components in question and in partial confirmation of the work of others in this field. A much more intensive study of the degradation products of each accelerator in mixes cured to varying degrees may well throw more light on the complex subject of accelerators. Although, therefore, the authors have been able to show the utility of chromatography for their own particular analytical problems, it is likely, ultimately, to be of great value in the exploration of some of the fundamental problems of rubber chemistry.


1980 ◽  
Vol 17 (1) ◽  
pp. 1-13 ◽  
Author(s):  
William D. Perreault ◽  
Forrest W. Young

The authors discuss and illustrate the advantages and limitations of a family of new approaches to the analysis of metric and nonmetric data in marketing research. The general method, which is based on alternating least squares optimal scaling procedures, extends the analytical flexibility of the general linear model procedures (ANOVA, regression, canonical correlation, discriminant analysis, etc.) to situations in which the data (1) are measured at any mixture of the nominal, ordinal, or interval levels and (2) are derived from either a discrete or continuous distribution. The relationship of these procedures to traditional linear models and to other nonmetric approaches (such as multidimensional scaling and conjoint analysis) is reviewed.


Paleobiology ◽  
1980 ◽  
Vol 6 (02) ◽  
pp. 146-160 ◽  
Author(s):  
William A. Oliver

The Mesozoic-Cenozoic coral Order Scleractinia has been suggested to have originated or evolved (1) by direct descent from the Paleozoic Order Rugosa or (2) by the development of a skeleton in members of one of the anemone groups that probably have existed throughout Phanerozoic time. In spite of much work on the subject, advocates of the direct descent hypothesis have failed to find convincing evidence of this relationship. Critical points are:(1) Rugosan septal insertion is serial; Scleractinian insertion is cyclic; no intermediate stages have been demonstrated. Apparent intermediates are Scleractinia having bilateral cyclic insertion or teratological Rugosa.(2) There is convincing evidence that the skeletons of many Rugosa were calcitic and none are known to be or to have been aragonitic. In contrast, the skeletons of all living Scleractinia are aragonitic and there is evidence that fossil Scleractinia were aragonitic also. The mineralogic difference is almost certainly due to intrinsic biologic factors.(3) No early Triassic corals of either group are known. This fact is not compelling (by itself) but is important in connection with points 1 and 2, because, given direct descent, both changes took place during this only stage in the history of the two groups in which there are no known corals.


Author(s):  
D. F. Blake ◽  
L. F. Allard ◽  
D. R. Peacor

Echinodermata is a phylum of marine invertebrates which has been extant since Cambrian time (c.a. 500 m.y. before the present). Modern examples of echinoderms include sea urchins, sea stars, and sea lilies (crinoids). The endoskeletons of echinoderms are composed of plates or ossicles (Fig. 1) which are with few exceptions, porous, single crystals of high-magnesian calcite. Despite their single crystal nature, fracture surfaces do not exhibit the near-perfect {10.4} cleavage characteristic of inorganic calcite. This paradoxical mix of biogenic and inorganic features has prompted much recent work on echinoderm skeletal crystallography. Furthermore, fossil echinoderm hard parts comprise a volumetrically significant portion of some marine limestones sequences. The ultrastructural and microchemical characterization of modern skeletal material should lend insight into: 1). The nature of the biogenic processes involved, for example, the relationship of Mg heterogeneity to morphological and structural features in modern echinoderm material, and 2). The nature of the diagenetic changes undergone by their ancient, fossilized counterparts. In this study, high resolution TEM (HRTEM), high voltage TEM (HVTEM), and STEM microanalysis are used to characterize tha ultrastructural and microchemical composition of skeletal elements of the modern crinoid Neocrinus blakei.


Sign in / Sign up

Export Citation Format

Share Document