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1.
J Patient Exp ; 8: 23743735211014036, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-34179442

RESUMO

At the onset of the COVID-19 pandemic, many senior patients in the USC-Keck Family Medicine clinics were limited or lacking in telemedicine participation. Three factors contributed: lack of video-enabled devices, technological literacy, and/or absence of Wi-Fi connectivity. We addressed the first 2 of these factors. Via phone contact, 9 patients agreed to receive donated Android or Apple devices and to trial instruction manuals for use. Donated equipment and instructions were prepared and delivered in accordance with pandemic guidelines. Follow-up calls indicated that 4 participants were able to set up their devices and 3 of whom had connected with their providers. The remaining 5 participants had not set up their devices by the end of the follow-up period, had difficulty with device setup, accessing applications necessary for telemedicine, or had limited access to Wi-Fi. This project highlights some telemedicine barriers that senior patients may overcome with the additional support of care providers.

2.
Nucleosides Nucleotides Nucleic Acids ; 37(1): 20-34, 2018 Jan 02.
Artigo em Inglês | MEDLINE | ID: mdl-29336673

RESUMO

The Corey-Bakshi-Shibata (CBS) catalyst provides an efficient mechanism to reduce ketones and achieve desired enantiopure alcohols. Herein, the diastereoselective reduction of C-2' and C-3'-keto ribofuranoside derivatives to the corresponding arabino- and xylofuranosides in greater than 95% diastereomeric excess is reported. The stereo-directed substitution with an azido group as well as the synthesis of prodrugs cytarabine and vidarabine are also described. The reported strategy offers superior diastereoselectivity, shorter reaction times, and obviates cooling required with comparable protocols involving achiral reductants.


Assuntos
Arabinonucleosídeos/síntese química , Glucosídeos/síntese química , Pró-Fármacos/síntese química , Catálise , Estrutura Molecular , Oxirredução , Estereoisomerismo , Vidarabina/síntese química
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