Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Más filtros

Banco de datos
Tipo del documento
Intervalo de año de publicación
1.
J Am Chem Soc ; 143(48): 20035-20041, 2021 12 08.
Artículo en Inglés | MEDLINE | ID: mdl-34817163

RESUMEN

Methylene-selective C-H functionalization is a significant hurdle that remains to be addressed in the field of Pd(II) catalysis. We report a Pd(II)-catalyzed synthesis of benzocyclobutenes by methylene-selective C(sp3)-H arylation of ketones. The reaction utilizes glycine as a transient directing group and a 2-pyridone ligand, which may govern the methylene selectivity by making intimate molecular associations with the substrate during concerted metalation-deprotonation. This reaction is shown to be highly selective for intramolecular methylene C(sp3)-H arylation, thus enabling sequential C(sp3)-H functionalization.

2.
Chem Soc Rev ; 47(23): 8925-8967, 2018 Dec 07.
Artículo en Inglés | MEDLINE | ID: mdl-30426998

RESUMEN

In this review, recent examples featuring C-H functionalization in the synthesis of complex natural products are discussed. A focus is given to the way in which C-H functionalization can influence the logical process of retrosynthesis, and the review is organized by the type and method of C-H functionalization.

3.
J Org Chem ; 80(19): 9603-9, 2015 Oct 02.
Artículo en Inglés | MEDLINE | ID: mdl-26393809

RESUMEN

4-(4-Nitrobenzyl)pyridine (NBP) is a colorimetric indicator compound for many types of carcinogenic alkylating agents. Because of the similar reactivity of NBP and guanine in DNA, NBP serves as a DNA model. NBP assays are used in the toxicological screening of pharmaceutical compounds, detection of chemical warfare agents, environmental hygiene technology, preliminary toxicology tests, mutagenicity of medicinal compounds, and other chemical analyses. Nevertheless, the use of NBP as a DNA model suffers from the compound's low water solubility, its lack of reactive oxygen sites, and dissimilar steric encumbrance compared to DNA. We report herein the design and synthesis of NBP derivatives that address some of these issues. These derivatives have been tested in solution and found to be superior in the colorimetric assay of the alkylating anticancer drug cyclophosphamide. The derivatives have also been integrated into a polymeric silica material which changes color upon the exposure to dangerous alkylating agents, such as iodomethane vapor, without the need for an exogenous base. This material modernizes the NBP assay from a time-consuming laboratory analysis to a real-time solid state sensor, which requires neither solvent nor additional reagents and can detect both gas- and solution-phase alkylating agents.


Asunto(s)
Alquilantes/síntesis química , Antineoplásicos/química , Ciclofosfamida/química , ADN/química , Indicadores y Reactivos/síntesis química , Piridinas/síntesis química , Alquilantes/química , Antineoplásicos/farmacología , Biomimética , Colorimetría , Ciclofosfamida/farmacología , Indicadores y Reactivos/química , Piridinas/química
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA