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2.
J Family Med Prim Care ; 9(12): 6158-6163, 2020 Dec.
Article in English | MEDLINE | ID: mdl-33681057

ABSTRACT

AIM: The aim of the cross-sectional study was to ascertain the oral health status and treatment needs of special health care need children of age group 3-16 years in rural and urban areas of Hyderabad, Telangana, India. MATERIALS AND METHOD: To assess and compare the caries status, oral health status, oral hygiene measures, diet and treatment needs in rural and urban population. The data collected was processed and analyzed using the SPSS statistical software program. RESULTS: Among 1000 subjects in rural and urban population highly significant difference was observed for Oral hygiene aids (P < 0.003) and for DMFT (P < 0.008) and no significant difference for dmft (P > 0.26). OHIs status showed no difference in primary and permanent in both rural and urban population (P > 1). Filled and missed were in DMFT, dmft was very low even though there were carious tooth in study population. Most of the children in rural and urban population required varied treatment needs like oral prophylaxis, restoration, pulp therapy, crowns and extractions. CONCLUSION: High prevalence of dental caries and the need for restorative care was noted in these children emphasizing the necessity of change of attitude towards oral health and improved oral care by repeated counselling of parents by primary health care physicians.

3.
Chem Commun (Camb) ; 49(68): 7519-21, 2013 Sep 04.
Article in English | MEDLINE | ID: mdl-23864053

ABSTRACT

We show that ultrasound-induced mechanical force isomerizes an azobenzene centered within a poly(methyl acrylate) polymer from cis to trans configuration without cleaving the azo bond. The isomerization rate was not altered by the polarity of the solvent indicating that the isomerization occurs through a non-polar, inversion transition state.


Subject(s)
Azo Compounds/chemistry , Molecular Structure , Polymers/chemical synthesis , Polymers/chemistry , Stereoisomerism
4.
J Org Chem ; 77(4): 2074-9, 2012 Feb 17.
Article in English | MEDLINE | ID: mdl-22283229

ABSTRACT

We describe a synthetic protocol to selectively functionalize chiral bridged triarylamines at the apical position using regioselective copper-catalyzed amination reaction. This protocol allows the coupling of diphenylamines with a sterically hindered but electronically activated aryl-Br bond in the presence of a sterically unhindered but electronically unactivated aryl-Br bond. The unactivated aryl-Br bond was utilized further to synthesize a chiral heterohelicene homodimer using Stille coupling.

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