HETEROCYCLIC COMPOUNDS IN BROWNING AND BROWNING/NITRITE MODEL SYSTEMS: OCCURRENCE, FORMATION MECHANISMS, FLAVOR CHARACTERISTICS AND MUTAGENIC ACTIVITY

Author(s):  
Takayuki Shibamoto
Author(s):  
Gaston Vernin ◽  
Jacques Metzger ◽  
Adel A. M. Sultan ◽  
Ahmed K. El-Shafei ◽  
Cyril Párkányi

Molecules ◽  
2019 ◽  
Vol 24 (7) ◽  
pp. 1252 ◽  
Author(s):  
Tatiana Soboleva ◽  
Lisa Berreau

Carbon monoxide-releasing molecules (CORMs) that enable the delivery of controlled amounts of CO are of strong current interest for applications in biological systems. In this review, we examine the various conditions under which CO is released from 3-hydroxyflavones and 3-hydroxy-4-oxoquinolines to advance the understanding of how these molecules, or derivatives thereof, may be developed as CORMs. Enzymatic pathways from quercetin dioxygenases and 3-hydroxy-4-oxoquinoline dioxygenases leading to CO release are examined, along with model systems for these enzymes. Base-catalyzed and non-redox-metal promoted CO release, as well as UV and visible light-driven CO release from 3-hydroxyflavones and 3-hydroxy-4-oxoquinolines, are summarized. The visible light-induced CO release reactivity of recently developed extended 3-hydroxyflavones and a 3-hydroxybenzo[g]quinolone, and their uses as intracellular CORMs, are discussed. Overall, this review provides insight into the chemical factors that affect the thermal and photochemical dioxygenase-type CO release reactions of these heterocyclic compounds.


Author(s):  
Chi-Tang Ho ◽  
Linda J. Bruechert ◽  
Yuangang Zhang ◽  
E-Mean Chiu

2018 ◽  
Vol 18 (4) ◽  
pp. 289-295 ◽  
Author(s):  
Phillip G. Hammer ◽  
Ruiqin Yi ◽  
Isao Yoda ◽  
H. James Cleaves ◽  
Michael P. Callahan

AbstractWe studied the radiolysis of a wide variety of N-heterocycles, including many of biological importance, and find that the majority are remarkably stable in the solid-state when subjected to large doses of ionizing gamma radiation from a 60Co source. Degradation of N-heterocycles as a function of dose rate and total dose was measured using high-performance liquid chromatography with UV detection. Many N-heterocycles show little degradation when γ-irradiated up to a total dose of ~1 MGy, which approximates hundreds of millions of years’ worth of radiation emitted in meteorite parent bodies due to slow radionuclide decay. Extrapolation of these results suggests that these N-heterocyclic compounds would be stable in dry parent bodies over solar system timescales. We suggest that the abundance of these N-heterocycles as measured presently in carbonaceous meteorites is largely reflective of their abundance at the time aqueous alteration stopped in their parent bodies and the absence of certain compounds in present-day samples is either due to the formation mechanisms or degradation which occurred during periods of aqueous alteration or thermal metamorphism.


2015 ◽  
Vol 2015 ◽  
pp. 1-11 ◽  
Author(s):  
Mingqing Wu ◽  
Chunyan Chang ◽  
Tao Li ◽  
Jian Zhou ◽  
Liping Zhao

A study is carried out on chemical constitution of sulfur compounds in MTBE and their formation mechanisms. These sulfur compounds are classified into three types: common sulfur compounds, newly formed sulfur compounds, and high boiling sulfur compounds. Common sulfur compounds which include mercaptans, low molecule sulfides and disulfides, are directly from C4, one of the stocks for production of MTBE. The newly formed sulfur compounds, with one sulfur atom and five or more total carbon atoms in one molecule, are mainly tert-butyl methyl sulfide and tert-butyl ethyl sulfide, thioetherification products of thiols with butenes. Many high boiling sulfur compounds, including polysulfides such as dimethyl trisulfide, multisulfur heterocyclic compounds such as 3,5-dimethyl-1,2,4-trithiolane, and oxygen-containing sulfur compounds such as 2-methoxy-3-methylthio-butane, are also found newly formed in the processes of LPG refining and succedent etherification reaction for producing MTBE. Polysulfides are additional products of elemental sulfur to disulfides, and other high boiling sulfur compounds may be formed by thiols reacting with dienes.


Author(s):  
B. Cunningham ◽  
D.G. Ast

There have Been a number of studies of low-angle, θ < 4°, [10] tilt boundaries in the diamond lattice. Dislocations with Burgers vectors a/2<110>, a/2<112>, a<111> and a<001> have been reported in melt-grown bicrystals of germanium, and dislocations with Burgers vectors a<001> and a/2<112> have been reported in hot-pressed bicrystals of silicon. Most of the dislocations were found to be dissociated, the dissociation widths being dependent on the tilt angle. Possible dissociation schemes and formation mechanisms for the a<001> and a<111> dislocations from the interaction of lattice dislocations have recently been given.The present study reports on the dislocation structure of a 10° [10] tilt boundary in chemically vapor deposited silicon. The dislocations in the boundary were spaced about 1-3nm apart, making them difficult to resolve by conventional diffraction contrast techniques. The dislocation structure was therefore studied by the lattice-fringe imaging technique.


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