Reaction products of dichloromethylenamides of dialkylphosphoric acids with amines and acetic anhydride

1974 ◽  
Vol 23 (6) ◽  
pp. 1317-1318
Author(s):  
L. A. Antokhina ◽  
P. I. Alimov
Keyword(s):  
Acetic Anhydride ◽  
Reaction Products

Reactions of phenyl-substituted heterocyclic compounds. VII. Reagent-dependent orientation in the nitration of 4-phenylpyrimidine

1967 ◽  
Vol 45 (13) ◽  
pp. 1431-1437 ◽  
Author(s):  
Brian M. Lynch ◽  
Lizzie Poon
Keyword(s):  
Nitric Acid ◽  
Acetic Anhydride ◽  
Nucleophilic Addition ◽  
Heterocyclic Compounds ◽  
Trifluoroacetic Anhydride ◽  
Reaction Products ◽  
Heterocyclic Nitrogen

In the nitration of 4-phenylpyrimidine, the nature of the reaction products is strongly dependent upon the nitrating reagent. Mixed nitric and sulfuric acids yield 4-o- and 4-m-nitrophenylpyrimidines in the ratio 2:3, whereas nitric acid – trifluoroacetic anhydride yields 4-o-, 4-m-, and 4-p-nitrophenylpyrimidines in the ratio 45:29:26, and nitric acid – acetic anhydride yields 2,4-diacetoxy-1,3,5-trinitro-6-phenyl-1,2,3,4-tetrahydropyrimidine.An explanation of these findings involves the possibility of the addition of nitronium ion at the heterocyclic nitrogen, followed in some circumstances by nucleophilic addition.

scholarly journals Preparation and activity of guanidinated or acetylated erabutoxins

1976 ◽  
Vol 153 (2) ◽  
pp. 217-222 ◽  
Author(s):  
H Hori ◽  
N Tamiya
Keyword(s):  
Circular Dichroism ◽  
Acetic Anhydride ◽  
Column Chromatography ◽  
Reaction Products ◽  
Amino Groups ◽  
Sea Snake ◽  
Lysine Residues ◽  
Erabutoxin B ◽  
Circular Dichroïsm

1. Erabutoxins, a, b and c, neurotoxic proteins of a sea snake Lacticauda semifasciata, were guanidinated with O-methylisourea. The amino groups of all the lysine residues and those at the N-termini of the toxins were modified. The lethal activity of the toxins decreased to 50% (erabutoxins a and b) or 17% (erabutoxin c) of the original value on the modification. The c.d. (circular dichroism) maximum at 227 nm of the modified toxins became lower, whereas the whole profile of the c.d. curve remained unchanged. 2. The amino groups of erabutoxin b were acetylated with acetic anhydride. All the five monoacetyl derivatives were isolated from the reaction products by CM-cellulose and Bio-Rex 70 column chromatography. [1-Nalpha-acetylarginine]-, [15-N6-acetyl-lysine]- and [51-N6-acetyl-lysine]-erabutoxin b retained the toxicity of the native toxin, whereas [27-N6-acetyl-lysine] and [47-N6-acetyl-lysine]-erabutoxin b were 17 and 8% active respectively. The overall profile of c.d. spectrum of erabutoxin b remained unchanged on the monoacetylation.

Unexpected Reaction Products of Uracil and Its Methyl Derivatives with Acetic Anhydride and Methylene Chloride

2021 ◽  
Author(s):  
Olga Michalak ◽  
Piotr Cmoch ◽  
Andrzej Leś ◽  
Marcin Cybulski ◽  
Piotr Krzeczyński ◽  
...  
Keyword(s):  
Acetic Anhydride ◽  
Methylene Chloride ◽  
Reaction Products ◽  
Unexpected Reaction ◽  
Methyl Derivatives

scholarly journals THE ESTIMATION OF SOME 17-ALKYL-SUBSTITUTED STEROIDS WITH THE ZINC CHLORIDE – ACETYL CHLORIDE (TSHUGAEV) REAGENT AND A POSTULATED REACTION MECHANISM

1951 ◽  
Vol 29 (2) ◽  
pp. 217-222 ◽  
Author(s):  
R. H. Cox ◽  
E. Y. Spencer
Keyword(s):  
Reaction Mechanism ◽  
Acetic Anhydride ◽  
Sulphuric Acid ◽  
Zinc Chloride ◽  
Acetyl Chloride ◽  
Maximum Absorption ◽  
Ring Cleavage ◽  
Reaction Products ◽  
Experimental Support

The reactivity of a number of 17-alkyl-substituted steroids toward the zinc chloride – acetyl chloride (Tshugaev) reagent has been investigated. Maximum absorption values of reaction products were determined spectrophotometrically. A general parallelism between the Liebermann–Burchard (sulphuric acid-acetic anhydride) and the Tshugaev reagent was confirmed except in the case of 5: 6 unsaturated 7-ketosteroids, which reacted to the latter reagent only. Arguments against currently suggested mechanisms for the Liebermann–Burchard reaction are presented, and a new mechanism for color production is postulated which involves ring cleavage. Experimental support is offered.

Ring Contractions of 3-Azido-4H-quinolizin-4-ones and 3-Azido-4H-azino[1,2 - x]pyrimidin-4-ones: a Novel Approach to 3-Aminoindolizines and their Aza Analogues

2008 ◽  
Vol 61 (2) ◽  
pp. 107 ◽  
Author(s):  
Simon Rečnik ◽  
Anton Meden ◽  
Branko Stanovnik ◽  
Jurij Svete
Keyword(s):  
Acetic Acid ◽  
Nmr Spectroscopy ◽  
Acetic Anhydride ◽  
Trifluoroacetic Anhydride ◽  
Reaction Products ◽  
Thermal Transformations ◽  
X Ray Diffraction ◽  
Ring Contraction ◽  
X Ray ◽  
Novel Approach

Thermal transformations of 3-azido-4H-quinolizin-4-ones 4a,b and 3-azido-4H-azino[1,2–x]pyrimidin-4-ones 4c,d, available from the corresponding heteroarylamines 2a–d, were studied. The reaction products were mostly dependent on the solvent. Thus, heating of 3-azido-1-cyano-4H-quinolizin-4-one (4a) in toluene afforded 2-(pyridin-2-yl)fumaronitrile 5a, whereas 3-amino-1-cyano-4H-quinolizin-4-one (8) was obtained on treatment of 4a in a mixture of toluene and trifluoroacetic anhydride. However, heating of 4a in acetic anhydride and in acetic acid resulted in a ring contraction to produce 3-(diacetylamino)indolizine-1-carbonitrile 6a and 3-(acetylamino)indolizine-1-carbonitrile 7a, respectively. Similarly, ring contractions took place on heating ethyl 3-azido-4-oxo-4H-quinolizin-1-carboxylate 4b and 3-azido-4H-azino[1,2–x]pyrimidin-4-ones 4c,d in acetic anhydride or acetic acid to produce the N-acetylated 3-aminoindolizine derivatives 6b, 7b and 3-aminoimidazo[1,2–x]azine derivatives 6c,d in 30–89% yields. The structures of compounds 5–8 were determined by NMR spectroscopy and X-ray diffraction.

Lead aspartate: a new en bloc stain for electron microscopy

1978 ◽  
Vol 36 (2) ◽  
pp. 34-35
Author(s):  
J.R. Walton
Keyword(s):  
Electron Microscopy ◽  
Calcium Ion ◽  
Enzyme Reaction ◽  
Lead Citrate ◽  
Reaction Products ◽  
En Bloc ◽  
Thin Sections ◽  
Lead Salts ◽  
Thin Sectioning ◽  
High Alkalinity

In electron microscopy, lead is the metal most widely used for enhancing specimen contrast. Lead citrate requires a pH of 12 to stain thin sections of epoxy-embedded material rapidly and intensively. However, this high alkalinity tends to leach out enzyme reaction products, making lead citrate unsuitable for many cytochemical studies. Substitution of the chelator aspartate for citrate allows staining to be carried out at pH 6 or 7 without apparent effect on cytochemical products. Moreover, due to the low, controlled level of free lead ions, contamination-free staining can be carried out en bloc, prior to dehydration and embedding. En bloc use of lead aspartate permits the grid-staining step to be bypassed, allowing samples to be examined immediately after thin-sectioning.Procedures. To prevent precipitation of lead salts, double- or glass-distilled H20 used in the stain and rinses should be boiled to drive off carbon dioxide and glassware should be carefully rinsed to remove any persisting traces of calcium ion.

Studies of Oxide Formation on Copper Thin Films by Electron Microscopy

1977 ◽  
Vol 35 ◽  
pp. 316-317
Author(s):  
G. G. Hembree ◽  
M. A. Otooni ◽  
J. M. Cowley
Keyword(s):  
Electron Microscopy ◽  
Electron Diffraction ◽  
Single Crystal ◽  
Crystal Surface ◽  
Crystal Defects ◽  
Diffraction Reflection ◽  
Reaction Products ◽  
Intermediate Energies ◽  
Crystal Films ◽  
Reflection Electron Microscopy

The formation of oxide structures on single crystal films of metals has been investigated using the REMEDIE system (for Reflection Electron Microscopy and Electron Diffraction at Intermediate Energies) (1). Using this instrument scanning images can be obtained with a 5 to 15keV incident electron beam by collecting either secondary or diffracted electrons from the crystal surface (2). It is particularly suited to studies of the present sort where the surface reactions are strongly related to surface morphology and crystal defects and the growth of reaction products is inhomogeneous and not adequately described in terms of a single parameter. Observation of the samples has also been made by reflection electron diffraction, reflection electron microscopy and replication techniques in a JEM-100B electron microscope.A thin single crystal film of copper, epitaxially grown on NaCl of (100) orientation, was repositioned on a large copper single crystal of (111) orientation.

Precipitation in silicon: Microanalysis

1988 ◽  
Vol 46 ◽  
pp. 474-475
Author(s):  
R.W. Carpenter
Keyword(s):  
Transition Metals ◽  
Spatial Resolution ◽  
Thin Foil ◽  
Precipitation Reaction ◽  
High Current ◽  
Reaction Products ◽  
Carbon And Nitrogen ◽  
Dielectric Layers ◽  
Precipitation Processes ◽  
Areas Of Interest

Interest in precipitation processes in silicon appears to be centered on transition metals (for intrinsic and extrinsic gettering), and oxygen and carbon in thermally aged materials, and on oxygen, carbon, and nitrogen in ion implanted materials to form buried dielectric layers. A steadily increasing number of applications of microanalysis to these problems are appearing. but still far less than the number of imaging/diffraction investigations. Microanalysis applications appear to be paced by instrumentation development. The precipitation reaction products are small and the presence of carbon is often an important consideration. Small high current probes are important and cryogenic specimen holders are required for consistent suppression of contamination buildup on specimen areas of interest. Focussed probes useful for microanalysis should be in the range of 0.1 to 1nA, and estimates of spatial resolution to be expected for thin foil specimens can be made from the curves shown in Fig. 1.

TEM characterization of reaction zone in a SiC fiber-reinforced titanium alloy

1988 ◽  
Vol 46 ◽  
pp. 738-739
Author(s):  
G. Das ◽  
R. E. Omlor
Keyword(s):  
Titanium Alloys ◽  
Reaction Zone ◽  
Carbon Layer ◽  
Fiber Reinforced ◽  
Reaction Products ◽  
Sic Fibers ◽  
Sic Fiber ◽  
The Matrix ◽  
Immense Potential

Fiber reinforced titanium alloys hold immense potential for applications in the aerospace industry. However, chemical reaction between the fibers and the titanium alloys at fabrication temperatures leads to the formation of brittle reaction products which limits their development. In the present study, coated SiC fibers have been used to evaluate the effects of surface coating on the reaction zone in the SiC/IMI829 system.IMI829 (Ti-5.5A1-3.5Sn-3.0Zr-0.3Mo-1Nb-0.3Si), a near alpha alloy, in the form of PREP powder (-35 mesh), was used a茸 the matrix. CVD grown AVCO SCS-6 SiC fibers were used as discontinuous reinforcements. These fibers of 142μm diameter contained an overlayer with high Si/C ratio on top of an amorphous carbon layer, the thickness of the coating being ∽ 1μm. SCS-6 fibers, broken into ∽ 2mm lengths, were mixed with IMI829 powder (representing < 0.1vol%) and the mixture was consolidated by HIP'ing at 871°C/0. 28GPa/4h.

Microstructural and fractographic characterization of B4C-Al cermets tested under dynamic and static loading

1989 ◽  
Vol 47 ◽  
pp. 562-563
Author(s):  
Gyeung Ho Kim ◽  
Mehmet Sarikaya ◽  
D. L. Milius ◽  
I. A. Aksay
Keyword(s):  
Thin Film ◽  
Mechanical Properties ◽  
Fracture Toughness ◽  
Static Loading ◽  
Carbon Deposition ◽  
Full Density ◽  
Unique Combination ◽  
Strong Component ◽  
Reaction Products

Cermets are designed to optimize the mechanical properties of ceramics (hard and strong component) and metals (ductile and tough component) into one system. However, the processing of such systems is a problem in obtaining fully dense composite without deleterious reaction products. In the lightweight (2.65 g/cc) B4C-Al cermet, many of the processing problems have been circumvented. It is now possible to process fully dense B4C-Al cermet with tailored microstructures and achieve unique combination of mechanical properties (fracture strength of over 600 MPa and fracture toughness of 12 MPa-m1/2). In this paper, microstructure and fractography of B4C-Al cermets, tested under dynamic and static loading conditions, are described.The cermet is prepared by infiltration of Al at 1150°C into partially sintered B4C compact under vacuum to full density. Fracture surface replicas were prepared by using cellulose acetate and thin-film carbon deposition. Samples were observed with a Philips 3000 at 100 kV.

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