Glioblastoma: current status, emerging targets, and recent advances

A Thakur, C Faujdar, R Sharma, S Sharma… - Journal of Medicinal …, 2022 - ACS Publications
Glioblastoma (GBM) is a highly malignant brain tumor characterized by a heterogeneous
population of genetically unstable and highly infiltrative cells that are resistant to …

Progress in the medicinal chemistry of silicon: C/Si exchange and beyond

S Fujii, Y Hashimoto - Future Medicinal Chemistry, 2017 - Taylor & Francis
Application of silyl functionalities is one of the most promising strategies among various
'elements chemistry'approaches for the development of novel and distinctive drug …

The role of silicon in drug discovery: a review

JL Panayides, DL Riley, F Hasenmaile… - RSC Medicinal …, 2024 - pubs.rsc.org
This review aims to highlight the role of silicon in drug discovery. Silicon and carbon are
often regarded as being similar with silicon located directly beneath carbon in the same …

Silicon switch: Carbon–silicon Bioisosteric replacement as a strategy to modulate the selectivity, physicochemical, and drug‐like properties in anticancer …

J Fotie, CM Matherne… - Chemical Biology & Drug …, 2023 - Wiley Online Library
Bioisosterism is one of the leading strategies in medicinal chemistry for the design and
modification of drugs, consisting in replacing an atom or a substituent with a different atom or …

Simmons–Smith Cyclopropanation: A Multifaceted Synthetic Protocol toward the Synthesis of Natural Products and Drugs: A Review

R Munir, AF Zahoor, S Javed, B Parveen, A Mansha… - Molecules, 2023 - mdpi.com
Simmons–Smith cyclopropanation is a widely used reaction in organic synthesis for
stereospecific conversion of alkenes into cyclopropane. The utility of this reaction can be …

Synthesis and anticancer and antiviral activities of C-2′-branched arabinonucleosides

M Bege, A Kiss, I Bereczki, J Hodek, L Polyák… - International Journal of …, 2022 - mdpi.com
d-Arabinofuranosyl-pyrimidine and-purine nucleoside analogues containing alkylthio-,
acetylthio-or 1-thiosugar substituents at the C2'position were prepared from the …

Synthesis of 4′/5′-Spirocyclopropanated Uridine and d-Xylouridine Derivatives and Their Activity against the Human Respiratory Syncytial Virus

C Köllmann, SM Wiechert, PG Jones… - Organic …, 2019 - ACS Publications
The Simmons–Smith–Furukawa reaction was used to generate 4′/5′-
spirocyclopropanated uridine analogs from electron-rich exocyclic enol esters. During …

Rhodium-catalyzed synthesis of Si-stereogenic alkoxysilanes and silyl enol ethers via hydrosilylation of carbonyl compounds

Y Ding, J Ke, W Zhang, B Li, C He - Chemical Communications, 2024 - pubs.rsc.org
A highly efficient rhodium-catalyzed asymmetric hydrosilylation of aldehydes, ketones, and
α, β-unsaturated ketones with dihydrosilanes is developed, that allows the rapid assembly of …

New 3-Aminopropylsilatrane Derivatives: Synthesis, Structure, Properties, and Biological Activity

SN Adamovich, IA Ushakov, EN Oborina… - International Journal of …, 2023 - mdpi.com
The biologically active compound 3-aminopropylsilatrane (a compound with a
pentacoordinated silicon atom) underwent an aza-Michael reaction with various acrylates …

Enantioselective synthesis of 4-Silyl-1, 2, 3, 4-tetrahydroquinolines via copper (I) hydride catalyzed asymmetric hydrosilylation of 1, 2-dihydroquinolines

QF Xu-Xu, P Yang, X Zhang, SL You - Synlett, 2021 - thieme-connect.com
C–Si bonds were constructed by utilizing copper hydride-catalyzed asymmetric
hydrosilylation of 1, 2-dihydroquinolines, affording various chiral 4-silyl-1, 2, 3, 4 …