Methoxydioxasilepane: A Versatile and Stable Synthetic Precursor of Trimethoxysilane

Abstract This study introduces aryl(methoxy)dioxasilepane as a versatile and stable precursor for aryl(trimethoxy)silanes. We conducted a quantitative assessment of the stability of this silicon moiety under acidic and basic conditions, demonstrating its superior stability compared to triethoxysilane, and methyl- or (trifluoroethoxy)dioxasilepanes. The synthetic utility of the methoxydioxasilepane unit was further elucidated through an examination of its orthogonality and selective functionalization capabilities. Notably, we developed an efficient method for the conversion of methoxydioxasilepane into trimethoxysilane. This method underscores the potential of a methoxydioxasilepane as a surrogate in multistep syntheses of silanetriols, which offer advantages in the development of silicon-based bioisosteres for medicinal chemistry applications.

Authors

Institutions

Publication Details

Journal
Synthesis
Published
2024-09-02
DOI
https://doi.org/10.1055/a-2408-7577
Citations
1
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.21

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Methoxydioxasilepane: A Versatile and Stable Synthetic Precursor of Trimethoxysilane

Hideki Yorimitsu, Jun Shimokawa, Hayate Saito, Kenshiro Hitoshio et al.
1 citations
Synthesis
Fluorine in Organic Chemistry
0.21
article

Methoxydioxasilepane: A Versatile and Stable Synthetic Precursor of Trimethoxysilane

Hideki Yorimitsu, Jun Shimokawa, Hayate Saito, Kenshiro Hitoshio, Hiroki Yamagishi, Takuto Morinaga, Ryohei Sahashi, Shinya Goshona
article en
1 citations

Abstract

Abstract This study introduces aryl(methoxy)dioxasilepane as a versatile and stable precursor for aryl(trimethoxy)silanes. We conducted a quantitative assessment of the stability of this silicon moiety under acidic and basic conditions, demonstrating its superior stability compared to triethoxysilane, and methyl- or (trifluoroethoxy)dioxasilepanes. The synthetic utility of the methoxydioxasilepane unit was further elucidated through an examination of its orthogonality and selective functionalization capabilities. Notably, we developed an efficient method for the conversion of methoxydioxasilepane into trimethoxysilane. This method underscores the potential of a methoxydioxasilepane as a surrogate in multistep syntheses of silanetriols, which offer advantages in the development of silicon-based bioisosteres for medicinal chemistry applications.

SynthesisVol. 57(08)
Kyoto University (JP)
Japan Society for the Promotion of Science, Japan Science and Technology Agency
Openalex Percentile: Top 51%
Fluorine in Organic Chemistry
0.21
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.