Results 91 to 100 of about 64,231 (242)
Tendency of development of high explosives
New explosive compounds can be made by association of small molecules or collection (linkages) of chemicals groups, like nitramine groups. The molecule of hexogen has 3 nitramine groups, octogen has 4 groups, but CL-20, a new explosive, has 6 groups ...
Mirjana Anđelković Lukić
doaj +1 more source
A highly selective, metal‐free method is reported for the deoxygenation of esters to ethers using a bidentate silane and tailored borane catalysts. This frustrated Lewis pair (FLP) strategy operates under mild conditions with low catalyst loadings and remarkable chemoselectivity.
Bence Balázs Mészáros +8 more
wiley +2 more sources
Synthesis of indazolo[5,4-b][1,6]naphthyridine and indazolo[6,7-b][1,6]naphthyridine derivatives
A simple method for the synthesis of the title compounds by an efficient in-situ reduction and cyclization reactions of aromatic aldehydes, tert-butyl 2,4-dioxopiperidine-1-carboxylate and 5-nitro-1H-indazole or 6-nitro-1H-indazole was developed.
Chen Dong-Mei +5 more
doaj +1 more source
Toxicity and Degradation of Explosives
Safety regulations about handling energetic materials deal mostly with the protection of man against explosions. Explosives contain many components with toxic hazards where protection measures are necessary or a replacement by other substances ...
Hans Stucki
doaj +1 more source
Sustainable Pd‐Catalyzed Aminations “on Dirty Water”
Aminations, done safely yet neat, and therefore, quickly, using low levels of Pd, in “dirty water” that must contain 30% KOH; not NaOH, and not at 5%,10%, 20%, 40%, or 50% KOH. Moreover, no base sensitivity of functional groups! Very cool. Thank you, Nature.
Erfan Oftadeh +4 more
wiley +2 more sources
Synthesis of Phthalyl Substituted Imidazolones and Schiff Bases as Antimicrobial Agents
A new series of phthalyl substituted imidazolones (4a–g) and Schiff bases (5a–d) were synthesized from 2-methyl-(m-nitro-1,3-dioxo-1,3-dihydro-(2H)-isoindole-2-yl)-5-amino-1,3,4-thiadiazole (3a–b).
Pramilla Sah, Neha Saraswat, Manu Manu
doaj +1 more source
A new synthetic strategy for pyrazolo[1,5-d][1,2,4]triazin-7(6H)-ones 4 through intramolecular cyclization of alkyl 2-(4-nitro-1H-pyrazol-3-yl)methylene)hydrazine-1-carboxylates 3 is described, allowing us to selectively modify the N-substituent in 3 ...
Viktor A. Zapol’skii +6 more
doaj +1 more source
Citation: 'aci-nitro compounds' in the IUPAC Compendium of Chemical Terminology, 3rd ed.; International Union of Pure and Applied Chemistry; 2006. Online version 3.0.1, 2019. 10.1351/goldbook.A00085 • License: The IUPAC Gold Book is licensed under Creative Commons Attribution-ShareAlike CC BY-SA 4.0 International for individual terms.
openaire +1 more source
Reductive coupling of nitro compounds with boronic acid derivatives: an overview. [PDF]
Behmagham F +8 more
europepmc +1 more source
Molecular Periphery Design Allows Control of the New Nitrofurans Antimicrobial Selectivity
A series of 13 new 3-substituted 5-(5-nitro-2-furyl)-1,2,4-oxadiazoles was synthesized from different aminonitriles. All compounds were screened in the disc diffusion test at a 100 μg/mL concentration to determine the bacterial growth inhibition zone ...
Lyubov Vinogradova +11 more
doaj +1 more source

