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1.
Acta Crystallogr Sect E Struct Rep Online ; 70(Pt 10): 192-5, 2014 Oct 01.
Artigo em Inglês | MEDLINE | ID: mdl-25484649

RESUMO

The title compound, C23H20N2O6S, crystallizes as a racemate in the space group P-1, with an overall L- or J-shape to each mol-ecule. Centrosymmetric pairs of mol-ecules are tandem hydrogen bonded between the hydro-per-oxy H atom and carbonyl O atom. A different centrosymmetric pairing has stacked S-tolyl rings, and a third pairing is L,J-inter-locked by the short leg. Except for stacked tolyl pairs, neighboring π-systems are much closer to orthogonal than coaxial. The title compound is the first example of a hydro-peroxide obtained from the autoxidation of a Diels-Alder adduct of a 2-vinyl-pyrrole.

2.
ACS Omega ; 9(9): 10201-10206, 2024 Mar 05.
Artigo em Inglês | MEDLINE | ID: mdl-38463253

RESUMO

Superabsorbent polymer (SAP) granules, typically used in personal care devices such as diapers, incontinence devices, hygiene pads, and wound dressings, and granular particles of zeolite and bentonite were each subjected to modification by exposure to solutions of 1-chloro-2,2,5,5-tetramethyl-4-imidazolidinone (MC) in ethanol at room temperature. The air-dried granules showed newly acquired properties attributable to the presence of active chlorine (Cl+). The treated particles effectively oxidized the malodorant 3-mercapto-3-methylbutanol (3M3MB). MC-treated granules inactivated urease, a microbial exoenzyme commonly involved in ammonia production. Modified SAP granules and superabsorbent fibers (SAFs) showed powerful antibacterial activity in an in vitro chronic wound model. The results suggest that processing of SAP granules and SAFs by this simple method at an industrial scale could add value to their widespread use in a variety of personal hygiene devices and specifically to the improvement of chronic wound care.

3.
Org Lett ; 8(2): 191-3, 2006 Jan 19.
Artigo em Inglês | MEDLINE | ID: mdl-16408872

RESUMO

[reaction: see text] A Lewis acid-catalyzed formal cycloaddition of alpha,beta-unsaturated aldehydes with 6-methyl-4-hydroxy-2-pyrone, 1,3-diketones, and vinylogous silyl esters is described here.


Assuntos
Aldeídos/química , Cetonas/química , Piranos/síntese química , Pironas/química , Compostos de Vinila/química , Catálise , Ciclização , Ésteres , Indicadores e Reagentes , Estrutura Molecular , Piranos/química , Estereoisomerismo
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